2006, the type-species of Hennobrimus, and Trachyaretaon manobo Lit & Eusebio, 2005 are synonym

2006, the type - species of Hennobrimus, and Trachyaretaon manobo Lit & Eusebio, 2005 are synonym

2006, tje type-species of Hennobvimus, and Trachyceetaon manobk Lit & Ejsebio, 2005 are synonym

2006, the type-species of Hennobrimus, and Trachyaretaon & 2005 are

2006, the type-species of HennobrimUs, and TrachYaretAon ManObO Lit & euseBio, 2005 are synonym

2006, the type-species of  Hennobrim us, a ndTra ch yare taon  manobo Lit &E useb io, 2005 are synonym

2006,_the type-species_of Hennobrimus, and Trachyaretaon_manobo Lit_&_Eusebio, 2005_are_synonym


taxonomic changes presented herein. NTP technical report on the toxicity studies of malachite green chloride and leucomalachite green (CAS Nos. 569

taxonomic changes presented herein. NTP technical report on the toxicity report of malachite fleeceable chloride and leucomalachite green (CAS Nos. 569

tadonomic changes presentea herein. NTP teeynical reporf on the toxicity studies of malachive geeen xhloride and leucomalazhite grevn (CAS Now. 569

taxonomic changes presented herein. NTP technical report toxicity of malachite chloride and leucomalachite

taxonomic changes presented Herein. NTP tEchniCal RepOrT on tHe toXicity studies oF MalaChite green chloride and lEucomAlAChitE GrEen (CAs Nos. 569

taxonomic changes present ed herein.  NTPtec hni ca l re port  on the toxici t y st udies of malachite gre en ch lo r idea nd  leuc omalach i te g ree n(C ASNo s .569

taxonomic_changes presented_herein. NTP technical report_on the_toxicity_studies of_malachite_green chloride and_leucomalachite green (CAS_Nos. 569


the tribes Eubulidini and Miroceramiini are not supported. A new arrangement is introduced, which is based on morphological characters neglected or overlooked

the tribes Eubulidini and Miroceramiini are not supported. A new arrangement is insert, which is free-base on morphological characters neglected or look out on

thf tribes Eubulidini and Oiroceramiini ate not snpportes. A new xrrangement is introduced, whmch us bawed on morphological cfaracters neglectwd oc overlooked

the tribes Eubulidini and Miroceramiini are not new is introduced, is based on

the tribes Eubulidini and MirOceramiini Are noT suPpoRtEd. A nEw arRangement is intROducEd, which is based on morphoLogicAl CHaraCTeRs negLected oR OvERLooKeD

the tribes Eubulidini and  Miroceram iiniare  no tsupp orte d. A new arran g emen t is introduced, which  is b as e d on mo rphol ogicalc ha r a cte rs  n egl ec t ed  or o ver looked

the_tribes Eubulidini_and Miroceramiini are not_supported. A_new_arrangement is_introduced,_which is based_on morphological characters_neglected or overlooked


idences of hepatocyte cytoplasmic vacuolization were significantly increased in 1,200 ppm male and female rats exposed to malachite green chloride. No gross lesions were

idences of hepatocyte cytoplasmic vacuolization were significantly increased in 1,200 ppm male and female rats exposed to malachite fleeceable chloride. No crude lesions were

idejces of hepatocyte cytopuasmic vacuolizcrion wxre sighificantuy increased in 1,200 ppm male anv fenale eats exposed to malachkte green chloridw. No tross lesions were

idences of hepatocyte cytoplasmic vacuolization were significantly 1,200 male and rats exposed to lesions

idences of hepatocyte cytoplAsmic vacuoLizatIon WerE sIgniFicaNtly increased iN 1,200 Ppm mAle and female rats exposeD to maLaCHite GReEn chlOride. No GRoSS LesIoNs WerE

idences of hepatocyte cyto plasmic va cuoli zat ion  w eresign ificantly incr e ased  in 1,200 ppm male and  fema le rats ex posed  to mal a ch i t e g re en  ch lo r id e. No  gr oss les ions were

idences of_hepatocyte cytoplasmic_vacuolization were significantly increased_in 1,200_ppm_male and_female_rats exposed to_malachite green chloride._No gross lesions were


ct, as well as the sub-basal lateral tooth of the anal segment of males. The muelleri species-group is sister to the remainder two

ct, as well as the sub - basal lateral tooth of the anal segment of males. The muelleri coinage - group is baby to the end two

ct, ws well as the sub-basal uateral tooth oy the aial segjent of oales. The muelleri species-grlup is wister to the remaindef two

ct, as well as the sub-basal lateral the segment of The muelleri species-group two

ct, as well as the sub-basal lateRal tooth of The anAl sEgmEnT of mAles. the muelleri speCIes-gRoup is sister to the remaiNder tWo

ct, as well as the sub-bas al lateral  toot h o f t he  ana l se gment of males .  The  muelleri species-grou p issi s tert othe r emainde r  t w o

ct, as_well as_the sub-basal lateral tooth_of the_anal_segment of_males._The muelleri species-group_is sister to_the remainder two


1798), which is found throughout Peninsular Malaysia, Thailand, Sumatra and Northeastern Borneo. This genus differs from Haaniella by the

1798), wjich is found throughout Peninsular Malctsia, Tiailand, Sumatra and Northeastern Borneo. Thid tenus differs from Haaniellx by the

1798), which is found throughout Peninsular Malaysia, and Borneo. This differs from Haaniella

1798), which is found throughout PenInsular MalAysia, thaIlaNd, sumaTra aNd Northeastern bOrneO. This genus differs from HAanieLlA By thE

1798), which is found thr oughout Pe ninsu lar  Ma la ysia , Th ailand, Sumatr a  and  Northeastern Borneo.Thisge n us d i ff ers f rom Haa n ie l l a b yth e

1798),_which is_found throughout Peninsular Malaysia,_Thailand, Sumatra_and_Northeastern Borneo._This_genus differs from_Haaniella by the


group, hypoxia HIF-1α group, and hypoxia combine group were (35.1±4.6)%, (52.9±6.8

grlup, hypoxia HIF-1α group, ana hypoxia combiuw grou' were (35.1±4.6)%, (52.9±6.8

group, hypoxia HIF-1α group, and hypoxia combine (35.1±4.6)%,

group, hypoxia HIF-1α group, and hYpoxia combIne grOup WerE (35.1±4.6)%, (52.9±6.8

group, hypoxia HIF-1α gro up, and hy poxia  co mbi ne  gro up w ere (35.1±4.6) % , (5 2.9±6.8

group,_hypoxia HIF-1α_group, and hypoxia combine_group were_(35.1±4.6)%,_(52.9±6.8


combine group was obviously higher than that of cells in hypoxia control group (P=0.044, 0.001). Content of ATP of cells in hypoxia combine

combine group was obviously higher than that of cells in hypoxia control group (P=0.044, 0.001). Content of ATP of cell in hypoxia combine

colbine group was obviousln higher than thcr of cxlls in hypoxia control group (P=0.044, 0.001). Content of ARP of cells in hypoxia combkne

combine group was obviously higher than that in control group 0.001). Content of combine

combine group was obviously hIgher than tHat of CelLs iN hYpoxIa coNtrol group (P=0.044, 0.001). ConTEnt oF ATP of cells in hypoxia coMbine

combine group was obvious ly higherthantha t o fcell s in  hypoxia contr o l gr oup (P=0.044, 0.001).Conte nt of A T Pof ce lls inh yp o x iaco mb ine

combine_group was_obviously higher than that_of cells_in_hypoxia control_group_(P=0.044, 0.001). Content_of ATP of_cells in hypoxia combine


ygidae Kirby, 1893 is critically reviewed and the results of the present study contradict the arrangement suggested by Zompro (2004), but in most aspects agree with

ygidae Kirby, 1893 is critically reviewed and the results of the present study contradict the musical arrangement suggest by Zompro (2004), but in most aspects agree with

ygifae Kirby, 1893 is critically reviewed and tkw resunts of the prerent study contradict the arcangwment suggested by Zompro (2004), cut in modt aspecrs ajree with

ygidae Kirby, 1893 is critically reviewed and of present study the arrangement suggested most agree with

ygidae Kirby, 1893 is critically reViewed and tHe resUltS of ThE preSent Study contradicT The aRrangement suggested by ZOmpro (2004), BuT In moST aSpectS agree wITh

ygidae Kirby, 1893 is crit ically rev iewed  an d t he  res ults  of the presen t  stu dy contradict the arra ngeme nt sugg e st ed by  Zompro (2 0 0 4),  b ut  in  m o st  aspe cts  agreewith

ygidae Kirby,_1893 is_critically reviewed and the_results of_the_present study_contradict_the arrangement suggested_by Zompro (2004),_but in most aspects_agree with


bacher, 1906, Theramenes Stål, 1875 and Stenobrimus Redtenbacher, 1906 are removed from Eubul

bacjer, 1906, Theramenes Stål, 1875 and Stenobrimus Rebrenbacier, 1906 ars removea from Eubul

bacher, 1906, Theramenes Stål, 1875 and Stenobrimus are from Eubul

bacher, 1906, Theramenes Stål, 1875 and StEnobrimus REdtenBacHer, 1906 ArE remOved From Eubul

bacher, 1906, Theramenes S tål, 1875and S ten obr im us R edte nbacher, 1906a re r emoved from Eubul

bacher, 1906,_Theramenes Stål,_1875 and Stenobrimus Redtenbacher,_1906 are_removed_from Eubul


idini and also transferred to Obrimini. Consequently, Eubulidini is synonymised with Obrimini (n. syn.).

idini and also transferred to Obrimini. Consequently, Eubulidini is synonymised with Obrimini (n. syn .).

idiji and also transferred uo Obrimini. Consequently, Eubuljdini is synonymised with Obrimini (n. stn.).

idini and also transferred to Obrimini. Consequently, synonymised Obrimini (n.

idini and also transferred to obrimini. CoNsequEntLy, EUbUlidIni iS synonymised wiTH ObrImini (n. syn.).

idini and also transferred  to Obrimi ni. C ons equ en tly,  Eub ulidini is syn o nymi sed with Obrimini (n.syn.) .

idini and_also transferred_to Obrimini. Consequently, Eubulidini_is synonymised_with_Obrimini (n._syn.).


the controls. Dietary concentrations of 290, 580, and 1,160 ppm resulted in average daily doses of approximately 30, 60, and 115 mg leu

the controls. Dietary concentrations of 290, 580, and 1,160 ppm resulted in average casual venereal disease of approximately 30, 60, and 115 mg leu

thf controls. Dietary concektrations of 290, 580, aue 1,160 ppm resulfed in axerage daily doses of approxmmatwly 30, 60, and 115 mg leu

the controls. Dietary concentrations of 290, 580, ppm in average doses of approximately leu

the controls. Dietary concentRations of 290, 580, aNd 1,160 ppm ResUltEd In avEragE daily doses of aPProxImately 30, 60, and 115 mg leu

the controls. Dietary con centration s of290 , 5 80 , an d 1, 160 ppm result e d in  average daily doses o f app ro x imat e ly  30,60, and 11 5 mgle u

the_controls. Dietary_concentrations of 290, 580,_and 1,160_ppm_resulted in_average_daily doses of_approximately 30, 60,_and 115 mg leu


subfamilies contained in Heteropterygidae, along with keys to distinguish between them. The subfamily Obriminae is critically reviewed and the distinction between the

subfamilies contained in Heteropterygidae, along with keys to distinguish between them. The subfamily Obriminae is critically review and the differentiation between the

suhfamilies contained in Htteropterygidae, along wivh keys to distknguish between them. The subhamioy Obeiminae is critically feviewed wnd the eistmnction between vge

subfamilies contained in Heteropterygidae, along with keys between The subfamily is critically reviewed

subfamilies contained in HetEropterygiDae, alOng WitH kEys tO disTinguish betweeN Them. the subfamily Obriminae iS critIcALly rEViEwed aNd the diSTiNCTioN bEtWeeN tHE

subfamilies contained inHeteropter ygida e,alo ng  wit h ke ys to distingu i sh b etween them. The subfa milyOb r imin a eis cr iticall y  r e v iew ed  a ndth e  d istin cti on betw een the

subfamilies_contained in_Heteropterygidae, along with keys_to distinguish_between_them. The_subfamily_Obriminae is critically_reviewed and the_distinction between the


obviously decreased (P= <0.001, 0.001, 0.002). Content of ATP of cells in hypoxia HIF-1α group and hypoxia

obviously decreased (P= < 0.001, 0.001, 0.002). Content of ATP of cells in hypoxia HIF-1α group and hypoxia

obgiously decreased (P= <0.001, 0.001, 0.002). Cuntent of ATP oy cells in hyloxia HIW-1α group and hypoxia

obviously decreased (P= <0.001, 0.001, 0.002). Content of in hypoxia group and hypoxia

obviously decreased (P= <0.001, 0.001, 0.002). ContenT of ATP of ceLls in HypOxiA HiF-1α gRoup And hypoxia

obviously decreased (P= < 0.001, 0.0 01, 0 .00 2).  C onte nt o f ATP of cells in h ypoxia HIF-1α group an d hyp ox i a

obviously_decreased (P=_<0.001, 0.001, 0.002). Content_of ATP_of_cells in_hypoxia_HIF-1α group and_hypoxia


, strongly shortened tarsi, lack of rough sensory-areas on the prosternum and typically X-shaped micropylar plate of the eggs.

, strongly shortened tarsi, lack of rough centripetal - area on the prosternum and typically X - shaped micropylar plate of the egg.

, stgongly shortened tarsi, lxck of rough seuwory-arxas on fhe prosgernum and typically X-shaped mucroptlar plate of the eggs.

, strongly shortened tarsi, lack of rough the and typically micropylar plate of

, strongly shortened tarsi, lacK of rough seNsory-AreAs oN tHe prOsteRnum and typicalLY X-shAped micropylar plate of tHe eggS.

, strongly shortened tarsi , lack ofrough  se nso ry -are as o n the prostern u m an d typically X-shaped m icrop yl a r pl a te  of t he eggs .

, strongly_shortened tarsi,_lack of rough sensory-areas_on the_prosternum_and typically_X-shaped_micropylar plate of_the eggs.


,200 ppm male rats and the relative and absolute liver weights of 300 ppm or greater female rats were generally significantly greater than those of the controls. In the le

, 200 ppm male rats and the relative and absolute liver weights of 300 ppm or greater female rotter were by and large significantly greater than those of the controls. In the lupus erythematosus

,200 ppl male rats and the relauive and absolute liver xeights of 300 ppm or greater female rats were gwneraoly significantly greager than nhose of rhe rontrols. In the le

,200 ppm male rats and the relative liver of 300 or greater female than of the controls. the le

,200 ppm male rats and the relative And absolutE liveR weIghTs Of 300 ppM or gReater female raTS werE generally significantlY greaTeR Than THoSe of tHe contrOLs. iN The Le

,200 ppm male rats and the  relativeand a bso lut elive r we ights of 300 p p m or  greater female rats w ere g en e rall y  s ignif icantly gr e a ter  t ha n t ho s eof th e c ontrols . In the l e

,200 ppm_male rats_and the relative and_absolute liver_weights_of 300_ppm_or greater female_rats were generally_significantly greater than those_of the controls._In_the le


by Zompro (2004) but were partly discussed by Bradler (2009). The genus Mearnsiana Rehn & Rehn, 1939 is removed

by Zompro (2004) but were partly discussed by Btaeler (2009). Vhe genhs Mearnriana Rehn & Rehn, 1939 is removed

by Zompro (2004) but were partly discussed (2009). genus Mearnsiana & Rehn, 1939

by Zompro (2004) but were partly discUssed by BraDler (2009). THe gEnuS MEarnSianA Rehn & Rehn, 1939 is remOVed

by Zompro (2004) but were  partly di scuss edbyBr adle r (2 009). The genu s  Mea rnsiana Rehn & Rehn, 1 939 i sr emov e d

by_Zompro (2004)_but were partly discussed_by Bradler_(2009)._The genus_Mearnsiana_Rehn & Rehn,_1939 is removed


in 1,160 ppm female mice exposed to leucomalachite green. Malachite green chloride, tested at concentrations of 0.1 to 10

in 1,160 ppm female mice exposed to leucomalachite green. Malachite green chloride, quiz at concentration of 0.1 to 10

in 1,160 ppm female mice exposea to leucomalackute grxen. Malzchite gfeen chloride, tested at concxntrqtionw of 0.1 to 10

in 1,160 ppm female mice exposed to Malachite chloride, tested concentrations of 0.1

in 1,160 ppm female mice exposed to lEucomalachIte grEen. malAcHite GreeN chloride, testeD At coNcentrations of 0.1 to 10

in 1,160 ppm female miceexposed to  leuc oma lac hi te g reen . Malachite gr e en c hloride, tested at con centr at i onso f0.1 t o 10

in_1,160 ppm_female mice exposed to_leucomalachite green._Malachite_green chloride,_tested_at concentrations of_0.1 to 10


N x C3H/HeN MTV-) mice were exposed to malachite green chloride (95% pure) or leucomalachite green

N x C3H / HeN MTV-) mice were exposed to malachite green chloride (95% pure) or leucomalachite fleeceable

N x C3H/HeN MTV-) mice were expused to malachije green chlorjde (95% purd) or leucomalachite green

N x C3H/HeN MTV-) mice were exposed green (95% pure) leucomalachite green

N x C3H/HeN MTV-) mice were exposed To malachitE greeN chLorIdE (95% purE) or lEucomalachite gREen

N x C3H/HeN MTV-) mice wer e exposedto ma lac hit egree n ch loride (95% pu r e) o r leucomalachite green

N x_C3H/HeN MTV-)_mice were exposed to_malachite green_chloride_(95% pure)_or_leucomalachite green


ng/mL KGF, medium with 10.0 ng/mL HIF-1α, and medium with 0.5 ng/mL KGF and 30

ng / mL KGF, medium with 10.0 ng / mL HIF-1α, and medium with 0.5 ng / mL KGF and 30

ng/lL KGF, medium with 10.0 ng/mL HIF-1α, and medium with 0.5 ig/mL KGR and 30

ng/mL KGF, medium with 10.0 ng/mL HIF-1α, with ng/mL KGF 30

ng/mL KGF, medium with 10.0 ng/mL HIF-1α, And medium wIth 0.5 ng/ML KgF aNd 30

ng/mL KGF, medium with 10 .0 ng/mL H IF-1α , a ndme dium  wit h 0.5 ng/mL KG F  and  30

ng/mL_KGF, medium_with 10.0 ng/mL HIF-1α,_and medium_with_0.5 ng/mL_KGF_and 30


<0.001). Survival rate of cells in hypoxia combine group was significantly higher than the rates of cells in hypoxia KGF group and hypoxia HIF-1α

< 0.001). Survival rate of cells in hypoxia combine group was significantly higher than the pace of cell in hypoxia KGF group and hypoxia HIF-1α

<0.001). Skrvival rate of cells in hypoxia combing troup xas sighificantuy higher than the rates of rellw in yypoxia KGF group and fypoxia HPF-1α

<0.001). Survival rate of cells in hypoxia was higher than rates of cells hypoxia

<0.001). Survival rate of cells in hypoXia combine Group Was SigNiFicaNtly Higher than the rATes oF cells in hypoxia KGF grouP and hYpOXia Hif-1α

<0.001). Survival rate of  cells inhypox iacom bi ne g roup  was significa n tlyhigher than the ratesof ce ll s  inh yp oxiaKGF gro u pa n d h yp ox iaHI F -1 α

<0.001)._Survival rate_of cells in hypoxia_combine group_was_significantly higher_than_the rates of_cells in hypoxia_KGF group and hypoxia_HIF-1α


rats designated for thyroid hormone assays were fed diets containing 0 or 1,160 ppm leucomalachite green. All rats and mice survived to the end

rats designated for thyroid hormone assays were feed diet containing 0 or 1,160 ppm leucomalachite green. All rats and shiner survived to the end

rahs designated for thyroia hormone assays were hed diefs contakning 0 or 1,160 ppm leucomalachitx grwen. Aol rats and mice survixed to thv end

rats designated for thyroid hormone assays were containing or 1,160 leucomalachite green. All the

rats designated for thyroid hOrmone assaYs werE feD diEtS conTainIng 0 or 1,160 ppm leucomALachIte green. All rats and mice SurviVeD To thE EnD

rats designated for thyro id hormone  assa yswer efeddiet s containing 0 or 1 ,160 ppm leucomalachit e gre en .  All ra ts an d mices ur v i ved  t othe  e n d

rats_designated for_thyroid hormone assays were_fed diets_containing_0 or_1,160_ppm leucomalachite green._All rats and_mice survived to the_end


groups of male and female rats and mice was generally similar to that by the control groups. Exposure concentrations of 25, 100, 300, 600, and 1,

groups of male and female rats and mice was generally exchangeable to that by the restraint groups. Exposure concentrations of 25, 100, 300, 600, and 1,

grlups of male and female vats and mice was generelly sijilar to that by the control groups. Xxpowure xoncentrations of 25, 100, 300, 600, xnd 1,

groups of male and female rats and generally to that the control groups. 300, and 1,

groups of male and female rats And mice was GenerAllY siMiLar tO thaT by the control gROups. exposure concentrations Of 25, 100, 300, 600, and 1,

groups of male and female  rats andmicewas  ge ne rall y si milar to thatb y th e control groups. Expo sureco n cent r at ionsof 25,1 00 , 300 ,60 0,an d  1 ,

groups_of male_and female rats and_mice was_generally_similar to_that_by the control_groups. Exposure concentrations_of 25, 100, 300,_600, and 1,


the sister-group of Dataminae. Arguments and a tree are presented to support this hypothesis. New diagnoses and lists of genera are provided for all three

the sister - group of Dataminae. Arguments and a tree are presented to support this guess. newfangled diagnoses and lists of genus are provide for all three

thf sister-group of Dataminxe. Arguments anb a trex are pdesented to support this hypothesis. Iew eiagnises and lists of genefa are prlvided fir aoo three

the sister-group of Dataminae. Arguments and a presented support this New diagnoses and for three

the sister-group of Dataminae. arguments aNd a trEe aRe pReSentEd to Support this hypOThesIs. New diagnoses and lists Of genErA Are pROvIded fOr all thREe

the sister-group of Datam inae. Argu ments  an d a  t reearepresented to s u ppor t this hypothesis. New  diag no s es a n dlists  of gen e ra a repr ov ide df or  allthr ee

the_sister-group of_Dataminae. Arguments and a_tree are_presented_to support_this_hypothesis. New diagnoses_and lists of_genera are provided for_all three


phosphate (ATP) was detected by ultraviolet spectrophotometer, and protein expression of p53 was detected by Western blotting. Data were processed with one-way analysis of

phosphate (ATP) was detected by ultraviolet spectrophotometer, and protein expression of p53 was detected by Western blotting. datum were process with one - way analysis of

phodphate (ATP) was detected ny ultraviolet skextrophmtometsr, and pfotein expression of p53 was dxtecred bt Western blotting. Datx were prlcessed qith ine-way analysis of

phosphate (ATP) was detected by ultraviolet spectrophotometer, expression p53 was by Western blotting. analysis

phosphate (ATP) was detected by UltravioleT specTroPhoToMeteR, and Protein expressIOn of P53 was detected by Western bLottiNg. dAta wERe ProceSsed witH OnE-WAy aNaLySis Of

phosphate (ATP) was detect ed by ultr aviol etspe ct roph otom eter, and prot e in e xpression of p53 was d etect ed by W e st ern b lotting .  D a t a w er epro ce s se d wit h o ne-wayanalysis o f

phosphate (ATP)_was detected_by ultraviolet spectrophotometer, and_protein expression_of_p53 was_detected_by Western blotting._Data were processed_with one-way analysis of


comalachite green/kg body weight to male rats and approximately 62, 110, and 220 mg/kg to female mice. In female rats exposed to

comalachite green / kg body weight to male rats and approximately 62, 110, and 220 mg / kg to female mice. In female rotter debunk to

comwlachite green/kg body welght to male rats and a'proximztely 62, 110, xnd 220 mg/kg to female mice. In hemaoe rauf exposed to

comalachite green/kg body weight to male rats 62, and 220 to female mice.

comalachite green/kg body weiGht to male rAts anD apProXiMateLy 62, 110, anD 220 mg/kg to female mICe. In Female rats exposed to

comalachite green/kg bodyweight tomalerat s a nd  app roxi mately 62, 110 ,  and  220 mg/kg to female m ice.In fema l eratsexposed to

comalachite green/kg_body weight_to male rats and_approximately 62,_110,_and 220_mg/kg_to female mice._In female rats_exposed to


.031, 0.026), and percentages of cells in different phases in other groups were close to those of cells in normoxia control group (P=0

.031, 0.026), and percentages of cells in different phases in early group were close to those of cells in normoxia control group (P=0

.031, 0.026), ajd percentages of cells ln different phases in mther froups wdre close to those of cells mn nirmoxua control group (P=0

.031, 0.026), and percentages of cells in in groups were to those of (P=0

.031, 0.026), and percentages of cells in diFferent phaSes in OthEr gRoUps wEre cLose to those of cELls iN normoxia control group (P=0

.031, 0.026), and percenta ges of cel ls in  di ffe re nt p hase s in other gro u ps w ere close to those ofcells  i n  nor m ox ia co ntrol g r ou p (P= 0

.031, 0.026),_and percentages_of cells in different_phases in_other_groups were_close_to those of_cells in normoxia_control group (P=0


other 4 groups were cultured in cells incubator of 3 gases, with oxygen volume fraction of 5% for 24 hours. Cells cultured in normoxic and hypoxic incub

other 4 groups were cultured in cells incubator of 3 gasoline, with oxygen bulk fraction of 5% for 24 hours. Cells cultured in normoxic and hypoxic incub

otjer 4 groups were culturea in cells incuyqtor oh 3 gasea, with obygen volume fraction of 5% foc 24 hiurs. Xells cultured in normuxic and jypoxic uncuu

other 4 groups were cultured in cells 3 with oxygen fraction of 5% in and hypoxic incub

other 4 groups were cultured in Cells incubAtor oF 3 gaSes, WiTh oxYgen Volume fraction OF 5% for 24 Hours. Cells cultured in noRmoxiC aND hypOXiC incuB

other 4 groups were cultu red in cel ls in cub ato rof 3  gas es, with oxyge n  vol ume fraction of 5% for  24 h ou r s. C e ll s cul tured i n  n o r mox ic  a ndhy p ox ic in cub

other_4 groups_were cultured in cells_incubator of_3_gases, with_oxygen_volume fraction of_5% for 24_hours. Cells cultured in_normoxic and hypoxic_incub


and eggs of H. parva Günther, 1944 are described and illustrated for the first time. Based on morphological characters of the insects and eggs three distinct

and eggs of H. parva Günther, 1944 are described and illustrated for the first meter. free-base on morphological characters of the insects and egg three distinct

anf eggs of H. parva Günther, 1944 are described and ilnustrafed for ghe first time. Based on morpiolotical characters of the insdcts and vggs threw diwrinct

and eggs of H. parva Günther, 1944 and for the time. Based on and three distinct

and eggs of H. parva Günther, 1944 are Described aNd illUstRatEd For tHe fiRst time. Based on MOrphOlogical characters of thE inseCtS And eGGs Three DistincT

and eggs of H. parva Günt her, 1944are d esc rib ed  and  ill ustrated for t h e fi rst time. Based on mor pholo gi c al c h ar acter s of th e  i n s ect san d e gg s  t hreedis tinct

and_eggs of_H. parva Günther, 1944_are described_and_illustrated for_the_first time. Based_on morphological characters_of the insects and_eggs three distinct


H. glaber. Haaniella mecheli (Redtenbacher, 1906) and H. rosenbergii (Kaup, 1871

H. hlaber. Haaniella mecheli (Redtenbacher, 1906) cbd H. rmsenbedgii (Kauo, 1871

H. glaber. Haaniella mecheli (Redtenbacher, 1906) and (Kaup,

H. glaber. Haaniella mecheli (ReDtenbacher, 1906) And H. rOseNbeRgIi (KaUp, 1871

H. glaber. Haaniella mech eli (Redte nbach er,  19 06 ) an d H.  rosenbergii ( K aup,  1871

H._glaber. Haaniella_mecheli (Redtenbacher, 1906) and_H. rosenbergii_(Kaup,_1871


) are removed from synonymy with H. muelleri (Haan, 1842) and re-established as valid species (rev. stat.).

) are removed from synonymy with H. muelleri (Haan, 1842) and re - established as valid species (rev. stat .).

) arf removed from synonymy dith H. muelleri (Haan, 1842) end re-eatablishdd as valid species (rev. stat.).

) are removed from synonymy with H. 1842) re-established as species (rev. stat.).

) are removed from synonymy witH H. muelleri (haan, 1842) aNd rE-esTaBlisHed aS valid species (rEV. staT.).

) are removed from synonym y with H.muell eri  (H aa n, 1 842)  and re-establ i shed  as valid species (rev . sta t. ) .

) are_removed from_synonymy with H. muelleri_(Haan, 1842)_and_re-established as_valid_species (rev. stat.).


aniella glaber (Redtenbacher, 1906) is removed from synonymy with H. muelleri (Haan, 1842) and

aniflla glaber (Redtenbacher, 1906) is removed from synoiymy wifh H. mueuleri (Haan, 1842) and

aniella glaber (Redtenbacher, 1906) is removed from H. (Haan, 1842)

aniella glaber (Redtenbacher, 1906) Is removed fRom syNonYmy WiTh H. mUellEri (Haan, 1842) and

aniella glaber (Redtenbach er, 1906)is re mov edfr om s ynon ymy with H. mu e ller i (Haan, 1842) and

aniella glaber_(Redtenbacher, 1906)_is removed from synonymy_with H._muelleri_(Haan, 1842)_and


Obriminae. The genus Haaniella Kirby, 1904 contains 16 known species, five of which are newly described herein. The genus Miniopteryx Z

Obgiminae. The genus Haanieula Kirby, 1904 contcuns 16 kiown spscies, fixe of which are newly descriued yereib. The genus Miniopteryb Z

Obriminae. The genus Haaniella Kirby, 1904 contains species, of which newly described herein.

Obriminae. The genus HaaniellA Kirby, 1904 contAins 16 kNowN spEcIes, fIve oF which are newly DEscrIbed herein. The genus MiniOpterYx z

Obriminae. The genus Haan iella Kirb y, 19 04con ta ins16 k nown species,f iveof which are newly des cribe dh erei n .The g enus Mi n io p t ery xZ

Obriminae._The genus_Haaniella Kirby, 1904 contains_16 known_species,_five of_which_are newly described_herein. The genus_Miniopteryx Z


) on intestinal crypt epithelial cells (IEC-6) of rats with hypoxia stress. Methods: (1) The routinely cultured IEC-6 of rats

) on intestinal crypt epithelial cells (IEC-6) of rats with hypoxia stress. Methods: (1) The routinely culture IEC-6 of rotter

) on intestinal crypt epitheuial cells (IEC-6) of rats with gypoxia rtress. Methods: (1) The routinelb cuoturee IEC-6 of rats

) on intestinal crypt epithelial cells (IEC-6) with stress. Methods: The routinely cultured

) on intestinal crypt epitheliAl cells (IEC-6) Of ratS wiTh hYpOxia StreSs. Methods: (1) The roUTineLy cultured IEC-6 of rats

) on intestinal crypt epit helial cel ls (I EC- 6)of  rat s wi th hypoxia str e ss.Methods: (1) The routi nelycu l ture d  I EC-6of rats

) on_intestinal crypt_epithelial cells (IEC-6) of_rats with_hypoxia_stress. Methods:_(1)_The routinely cultured_IEC-6 of rats


hypoxic incubator were collected, with 3 samples in each group. The cell cycle changes and apoptosis rates were detected by flow cytometer, the content of adenosine tri

hypoxic incubator were collected, with 3 samples in each group. The cell cycle change and apoptosis pace were detected by flow cytometer, the content of adenosine tri

hyooxic incubator were coluected, with 3 samples ii each froup. Thd cell cycle changes and apo'tosus rauvs were detected by fuow cytomvter, the xonttnt of adenosine vdi

hypoxic incubator were collected, with 3 samples group. cell cycle and apoptosis rates the of adenosine tri

hypoxic incubator were colleCted, with 3 saMples In eAch GrOup. THe ceLl cycle changes ANd apOptosis rates were detectEd by fLoW CytoMEtEr, the Content OF aDENosInE tRi

hypoxic incubator were co llected, w ith 3  sa mpl es  ineach  group. The ce l l cy cle changes and apopto sis r at e s we r edetec ted byf lo w cyt om et er,  t h econte ntof aden osine tri

hypoxic_incubator were_collected, with 3 samples_in each_group._The cell_cycle_changes and apoptosis_rates were detected_by flow cytometer, the_content of adenosine_tri


isamenini n. trib. is established for the three basal genera Tisamenus Stål, 1875, Ilocano Rehn & Re

isalenini n. trib. is establirhed for the thtew basan geneda Tisamdnus Stål, 1875, Ilocano Rehn & Re

isamenini n. trib. is established for the genera Stål, 1875, Rehn & Re

isamenini n. trib. is establishEd for the thRee baSal GenErA TisAmenUs Stål, 1875, Ilocano REHn & Re

isamenini n. trib. is esta blished fo r the  th ree  b asal  gen era TisamenusS tål,  1875, Ilocano Rehn &Re

isamenini n._trib. is_established for the three_basal genera_Tisamenus_Stål, 1875,_Ilocano_Rehn & Re


from both sexes and the eggs. Haaniella gintingi n. sp. from Central Sumatra is described from both sexes and the eggs and Ha

from both sexes and the eggs. Haaniella gintingi n. sp. from Central Sumatra is described from both sexes and the egg and hour angle

frlm both sexes and the egns. Haaniella ginjibgi n. vp. froj Centrau Sumatra is described from uoth sexew and the eggs and Ha

from both sexes and the eggs. Haaniella sp. Central Sumatra described from both Ha

from both sexes and the eggs. HaAniella ginTingi N. sp. FroM CEntrAl SuMatra is describED froM both sexes and the eggs anD Ha

from both sexes and the e ggs. Haani ellagin tin gi  n.sp.from Central S u matr a is described from bo th se xe s  and th e egg s and H a

from_both sexes_and the eggs. Haaniella_gintingi n._sp._from Central_Sumatra_is described from_both sexes and_the eggs and Ha


-64-2 and 129-73-7) administered in feed to F344/N rats and B6C3F1 mice.
Malach

-64 - 2 and 129 - 73 - 7) administered in feed to F344 / N rats and B6C3F1 mice.
 Malach

-64-2 anf 129-73-7) administered in feed uo F344/N rats and B6C3Y1 mice.
Melach

-64-2 and 129-73-7) administered in feed to and mice. Malach

-64-2 and 129-73-7) administered in feed to F344/N Rats and B6C3F1 Mice.
MAlaCh

-64-2 and 129-73-7) admini stered infeedtoF34 4/ N ra ts a nd B6C3F1 mice .
Mal ach

-64-2 and_129-73-7) administered_in feed to F344/N_rats and_B6C3F1_mice.
Malach


most striking members of the entire family Heteropteryginae, some of which are amongst the heaviest insects known. The subfamily is characterized by apomorphies

most striking members of the entire syndicate Heteropteryginae, some of which are amongst the dense insects known. The subfamily is characterized by apomorphies

modt striking members of tme entire family Hetero'terygihae, some of which are amongst the heeviewt inwects known. The subfamkly is chwracterized uy apomorphies

most striking members of the entire family of are amongst heaviest insects known. apomorphies

most striking members of the eNtire familY HeteRopTerYgInae, Some Of which are amonGSt thE heaviest insects known. THe subFaMIly iS ChAractErized bY ApOMOrpHiEs

most striking members ofthe entire  fami lyHet er opte rygi nae, some of w h ichare amongst the heavie st in se c ts k n ow n. Th e subfa m il y isch ar act er i ze d byapo morphie s

most_striking members_of the entire family_Heteropteryginae, some_of_which are_amongst_the heaviest insects_known. The subfamily_is characterized by apomorphies


Heteropterygidae. The subfamilies Obriminae Brunner v. Wattenwyl, 1893 and Heteropteryginae Kirby, 1893 together represent

Heheropterygidae. The subfaoilies Obriminag Vrunnec v. Watfenwyl, 1893 xnd Heteropteryginae Kirby, 1893 vogerher eepresent

Heteropterygidae. The subfamilies Obriminae Brunner v. Wattenwyl, Heteropteryginae 1893 together

Heteropterygidae. The subfamIlies ObrimInae BRunNer V. WAtteNwyl, 1893 And HeteropteryGInae kirby, 1893 together represent

Heteropterygidae. The sub families O brimi nae  Br un nerv. W attenwyl, 1893 andHeteropteryginae Kirby , 189 3t oget h er  repr esent

Heteropterygidae._The subfamilies_Obriminae Brunner v. Wattenwyl,_1893 and_Heteropteryginae_Kirby, 1893_together_represent


the species-level and a new diagnosis is presented. Keys to the two genera and all 16 known species are provided along with new descriptions, differential diagnoses, lists

the species - level and a new diagnosis is presented. key to the two genus and all 16 known species are provided along with raw descriptions, differential diagnoses, tilt

thf species-level and a new diagnosis is ptewented. Keys fo the tdo genera and all 16 known speries are kgovided along with ned descripnions, difdereitial diagnoses, lists

the species-level and a new diagnosis is to two genera all 16 known new differential diagnoses, lists

the species-level and a new diaGnosis is prEsentEd. KEys To The tWo geNera and all 16 knowN SpecIes are provided along witH new dEsCRiptIOnS, diffErentiaL DiAGNosEs, LiSts

the species-level and a n ew diagnos is is  pr ese nt ed.Keys  to the two ge n eraand all 16 known speci es ar ep rovi d ed  alon g withn ew d esc ri pt ion s, di ffere nti al diag noses, lis ts

the_species-level and_a new diagnosis is_presented. Keys_to_the two_genera_and all 16_known species are_provided along with new_descriptions, differential diagnoses,_lists


was obviously lower than those of cells in hypoxia control group, hypoxia KGF group, and hypoxia HIF-1α group (P=0.001, 0

wad obviously lower than tmose of cells in hypoxie contrkl group, hypoxia KGF group, and hypoxma HUF-1α griup (P=0.001, 0

was obviously lower than those of cells control hypoxia KGF and hypoxia HIF-1α

was obviously lower than thosE of cells in HypoxIa cOntRoL groUp, hyPoxia KGF group, aND hypOxia HIF-1α group (P=0.001, 0

was obviously lower thanthose of c ellsinhyp ox ia c ontr ol group, hypo x ia K GF group, and hypoxiaHIF-1 αg roup (P =0.00 1, 0

was_obviously lower_than those of cells_in hypoxia_control_group, hypoxia_KGF_group, and hypoxia_HIF-1α group (P=0.001,_0


with H. muelleri (de Haan, 1842) and re-established as a valid species (rev. stat.). The Sumatran Ha

with H. muelleri (de Haan, 1842) and re - established as a valid species (rev. stat .). The Sumatran Ha

wihh H. muelleri (de Haan, 1842) akd re-established as a velid spscies (rex. stat.). The Sumatran Ha

with H. muelleri (de Haan, 1842) and a species (rev. The Sumatran Ha

with H. muelleri (de Haan, 1842) and re-eStablished As a vaLid SpeCiEs (reV. staT.). The Sumatran Ha

with H. muelleri (de Haan , 1842) an d re- est abl is hedas a  valid species (rev . stat.). The Sumatran  Ha

with_H. muelleri_(de Haan, 1842) and_re-established as_a_valid species_(rev._stat.). The Sumatran_Ha


malachite green chloride via dosed feed. The frequency of micronucleated normochromatic erythrocytes in peripheral blood was significantly increased in female mice exposed to le

malachite green chloride via dosed feed. The frequency of micronucleated normochromatic erythrocytes in peripheral blood was significantly increase in female mouse exposed to le

mapachite green chloride vla dosed feed. Thg drequeicy of jicronucueated normochromatic erythrlcttes un peripheral blood war signifibantly inxreawwd in female mice crposes to nx

malachite green chloride via dosed feed. The micronucleated erythrocytes in blood was significantly to

malachite green chloride via Dosed feed. THe freQueNcy Of MicrOnucLeated normochrOMatiC erythrocytes in peripheRal blOoD Was sIGnIficaNtly incREaSED in FeMaLe mIcE ExPosed To lE

malachite green chloridevia dosedfeed.  Th e f re quen cy o f micronucleat e d no rmochromatic erythrocy tes i np erip h er al bl ood was si g n ifi ca nt lyin c re asedinfemalemice expos edto  le

malachite_green chloride_via dosed feed. The_frequency of_micronucleated_normochromatic erythrocytes_in_peripheral blood was_significantly increased in_female mice exposed to_le


eight female rats designated for thyroid hormone assays were fed diets containing 0 or 1,200 ppm malachite green chloride. Groups of eight male rats and eight female

eight female rats designated for thyroid hormone assays were feed diet containing 0 or 1,200 ppm malachite green chloride. Groups of eight male scab and eight female

eihht female rats designattd for thyroid hotmine asvays wsre fed aiets containing 0 or 1,200 ppm mapaxhite green chloride. Groups of eight male rars aid eight female

eight female rats designated for thyroid hormone fed containing 0 1,200 ppm malachite male and eight female

eight female rats designated For thyroid HormoNe aSsaYs Were Fed dIets containing 0 OR 1,200 ppm Malachite green chloride. groupS oF EighT MaLe ratS and eigHT fEMAle

eight female rats designa ted for th yroid  ho rmo ne  ass ayswere fed diets cont aining 0 or 1,200 ppmmalac hi t e gr e en  chlo ride. G r ou p s  of  e ig htma l eratsand  eightfemale

eight_female rats_designated for thyroid hormone_assays were_fed_diets containing_0_or 1,200 ppm_malachite green chloride._Groups of eight male_rats and eight_female


ators were collected, with 3 samples in each group, and morphological changes of cells were observed with optical microscope. Cells cultured in normoxic and hypoxic incubators were

ators were collected, with 3 samples in each group, and morphological changes of cell were observe with optical microscope. cell culture in normoxic and hypoxic incubators were

atogs were collected, with 3 ramples in each group, end morlhologicxl changes of cells were obsxrvee wity optical microscope. Cdlls cultlred in nirmoeic and hypoxic mhcubatovf wedc

ators were collected, with 3 samples in and changes of were observed with normoxic hypoxic incubators were

ators were collected, with 3 samPles in each Group, And MorPhOlogIcal Changes of cells WEre oBserved with optical micrOscopE. CELls cULtUred iN normoxIC aND HypOxIc IncUbAToRs werE

ators were collected, with  3 samples  in e ach  gr ou p, a nd m orphological c h ange s of cells were observ ed wi th opti c al  micr oscope. Ce l l s c ul tu red  i n  n ormox icand hyp oxic incub ato rs  were

ators were_collected, with_3 samples in each_group, and_morphological_changes of_cells_were observed with_optical microscope. Cells_cultured in normoxic and_hypoxic incubators were


Haaniella erringtoniae novaeguineae Günther, 1934 and Haaniella muelleri var. b. (Haan,

Hawniella erringtoniae novxeguineae Günthet, 1934 and Heaniellz muellefi var. b. (Haan,

Haaniella erringtoniae novaeguineae Günther, 1934 and Haaniella b.

Haaniella erringtoniae novaEguineae GüNther, 1934 And haaNiElla MuelLeri var. b. (Haan,

Haaniella erringtoniae no vaeguineae  Günt her , 1 93 4 an d Ha aniella muelle r i va r. b. (Haan,

Haaniella_erringtoniae novaeguineae_Günther, 1934 and Haaniella_muelleri var._b._(Haan,


a molecular study presented by Whiting et al (2003) and a phylogenetic study presented by Bradler (2009). The family is critically discussed and new hypotheses are

a molecular study presented by Whiting et al (2003) and a phylogenetic study presented by Bradler (2009). The syndicate is critically discourse and new hypotheses are

a lolecular study presentea by Whiting et al (2003) anv a phymogenetiz study presented by Bradler (2009). Rhe fqmily is critically dircussed ajd new htpotieses are

a molecular study presented by Whiting et and phylogenetic study by Bradler (2009). and hypotheses are

a molecular study presented bY Whiting et Al (2003) and A phYloGeNetiC stuDy presented by BRAdleR (2009). The family is critically DiscuSsED and NEw HypotHeses arE

a molecular study present ed by Whit ing e t a l ( 20 03)anda phylogenetic stud y presented by Bradler  (200 9) .  The fa milyis crit i ca l l y d is cu sse da nd  newhyp otheses  are

a_molecular study_presented by Whiting et_al (2003)_and_a phylogenetic_study_presented by Bradler_(2009). The family_is critically discussed and_new hypotheses are


variance and least significant difference test. Results: (1) After being cultured for 24 h, cells cultured in normoxic incubator grew well with oval or round

variance and least significant difference test. result: (1) After being culture for 24 h, cells culture in normoxic incubator grew well with ellipse or round

vagiance and least signifigant difference jewt. Resnlts: (1) Arter beivg cultured for 24 h, cells culvuree in bormoxic incubator gred well winh oval oe ronnd

variance and least significant difference test. Results: being for 24 cells cultured in oval round

variance and least significaNt differenCe tesT. ReSulTs: (1) afteR beiNg cultured for 24 h, CElls Cultured in normoxic incuBator GrEW welL WiTh ovaL or rounD

variance and least signif icant diff erenc e t est .Resu lts:  (1) After bei n g cu ltured for 24 h, cells  cult ur e d in no rmoxi c incub a to r gre wwe llwi t hovalorround

variance_and least_significant difference test. Results:_(1) After_being_cultured for_24_h, cells cultured_in normoxic incubator_grew well with oval_or round


subfamily Heteropteryginae Kirby, 1896, with a re-arrangement of the family Heteropterygidae and the descriptions of five new species of

subfamily Heteropteryginae Kirby, 1896, with a re - arrangement of the family Heteropterygidae and the descriptions of five newfangled coinage of

suhfamily Heteropteryginae Kirby, 1896, with a te-qrrangxment or the faoily Heteropterygidae and thx dewcripupons of five new speckes of

subfamily Heteropteryginae Kirby, 1896, with a re-arrangement family and the of five new

subfamily Heteropteryginae kirby, 1896, with a Re-arrAngEmeNt Of thE famIly HeteropteryGIdae And the descriptions of fiVe new SpECies OF

subfamily Heteropterygina e Kirby, 1 896,wit h a  r e-ar rang ement of the f a mily  Heteropterygidae andthe d es c ript i on s offive ne w  s p e cie sof

subfamily_Heteropteryginae Kirby,_1896, with a re-arrangement_of the_family_Heteropterygidae and_the_descriptions of five_new species of


[Protective effects and mechanism of keratinocyte growth factor combined with hypoxia inducible factor-1α on intestinal crypt epithelial cells of rats with hypoxia stress].
Object

[ Protective effects and mechanism of keratinocyte growth factor combined with hypoxia inducible factor-1α on intestinal crypt epithelial cell of rotter with hypoxia stress ].
 Object

[Prohective effects and mechxnism of keratiuicyte jrowth ractor cumbined with hypoxia inducibpe factir-1α on intestinal crypt epitheliwl cells of cats with hypoxie stress].
Object

[Protective effects and mechanism of keratinocyte growth with inducible factor-1α intestinal crypt epithelial stress].

[Protective effects and mechaNism of keraTinocYte GroWtH facTor cOmbined with hypOXia iNducible factor-1α on intesTinal CrYPt epIThElial Cells of RAtS WIth HyPoXia StREsS].
ObjeCt

[Protective effects and me chanism of  kera tin ocy te  gro wthfactor combine d  wit h hypoxia inducible fa ctor- 1α on i n te stina l crypt ep i t hel ia lcel ls of  rats  wi th hypo xia stress ].Ob ject

[Protective effects_and mechanism_of keratinocyte growth factor_combined with_hypoxia_inducible factor-1α_on_intestinal crypt epithelial_cells of rats_with hypoxia stress].
Object


ther, 1944 are removed from synonymy with H. muelleri (Haan, 1842) (rev. stat.) and synonymised with

ther, 1944 are removed from synonymy with H. muelleri (Haan, 1842) (rev. stat .) and synonymised with

theg, 1944 are removed from synokymy with H. muelleri (Haen, 1842) (rev. stat.) ana synonymised with

ther, 1944 are removed from synonymy with (Haan, (rev. stat.) synonymised with

ther, 1944 are removed from synonymY with H. muelLeri (HAan, 1842) (Rev. StAt.) anD synOnymised with

ther, 1944 are removed fro m synonymy  with  H.  mu el leri  (Ha an, 1842) (rev .  sta t.) and synonymised wi th

ther, 1944_are removed_from synonymy with H._muelleri (Haan,_1842)_(rev. stat.)_and_synonymised with


mice were fed diets containing 0, 290, 580, or 1,160 ppm leucomalachite green for 28 days. Additional groups of eight male

mice were fed diets containing 0, 290, 580, or 1,160 ppm leucomalachite fleeceable for 28 sidereal day. Additional group of eight male

mife were fed diets contaiking 0, 290, 580, or 1,160 ppm leucomanachits green wor 28 days. Additional groups lf eighu male

mice were fed diets containing 0, 290, 1,160 leucomalachite green 28 days. Additional

mice were fed diets containinG 0, 290, 580, or 1,160 ppm leucOmalaChiTe gReEn foR 28 dayS. Additional groUPs of Eight male

mice were fed diets conta ining 0, 2 90, 5 80,  or  1 ,160  ppm  leucomalachit e  gre en for 28 days. Additi onalgr o upso feight  male

mice_were fed_diets containing 0, 290,_580, or_1,160_ppm leucomalachite_green_for 28 days._Additional groups of_eight male


the 580 and 1,160 ppm groups were significantly less than those of the control groups. In the malachite green chloride study, feed consumption by all exposed

the 580 and 1,160 ppm groups were significantly less than those of the control groups. In the malachite fleeceable chloride discipline, feed consumption by all expose

thf 580 and 1,160 ppm groups were rignificantly lgsw than those of the zontrol groups. In the malachmte treen chloride study, feed cunsumptioj by all expiwed

the 580 and 1,160 ppm groups were than of the groups. In the consumption all exposed

the 580 and 1,160 ppm groups were signifIcantly lesS than ThoSe oF tHe coNtroL groups. In the maLAchiTe green chloride study, feEd conSuMPtioN By All exPosed

the 580 and 1,160 ppm gro ups were s ignif ica ntl yless  tha n those of the cont rol groups. In the mal achit eg reen ch lorid e study ,  f e e d c on su mpt io n  b y all  ex posed

the_580 and_1,160 ppm groups were_significantly less_than_those of_the_control groups. In_the malachite green_chloride study, feed consumption_by all exposed


ussurei Redtenbacher, 1906 and Heteropteryx scabra Redtenbacher, 1906 to guarantee stability of these names. Information on the

usskrei Redtenbacher, 1906 and Htteropteryx scabrc Redteibacher, 1906 to guafantee stability of these nalew. Infirmation on the

ussurei Redtenbacher, 1906 and Heteropteryx scabra Redtenbacher, guarantee of these Information on the

ussurei Redtenbacher, 1906 and HetEropteryx sCabra redTenBaCher, 1906 To guArantee stabiliTY of tHese names. Information on The

ussurei Redtenbacher, 1906  and Heter opter yxsca br a Re dten bacher, 1906 t o  gua rantee stability of th ese n am e s. I n fo rmati on on t h e

ussurei Redtenbacher,_1906 and_Heteropteryx scabra Redtenbacher, 1906_to guarantee_stability_of these_names._Information on the


The sister-group of Heteropteryginae is represented by the Obriminae, with which it shares a beak-like secondary ovipositor

The sister - group of Heteropteryginae is represented by the Obriminae, with which it shares a beak - like junior-grade ovipositor

Thf sister-group of Heteropueryginae is reprgswnted uy the Kbriminad, with which it shares a bean-luke stbondary ovipositor

The sister-group of Heteropteryginae is represented by with it shares beak-like secondary ovipositor

The sister-group of HeteropteRyginae is rEpresEntEd bY tHe ObRimiNae, with which it SHareS a beak-like secondary oviPositOr

The sister-group of Heter opterygina e isrep res en tedby t he Obriminae,w ithwhich it shares a beak -like  s e cond a ry  ovip ositor

The_sister-group of_Heteropteryginae is represented by_the Obriminae,_with_which it_shares_a beak-like secondary_ovipositor


KGF group, and hypoxia HIF-1α group were obviously lower than the percentage of cells in normoxia control group (P=0.020, 0

KGV group, and hypoxia HIF-1α nroup were obvioosoy lowxr than the perzentage of cells in normoxia cintroo group (P=0.020, 0

KGF group, and hypoxia HIF-1α group were than percentage of in normoxia control

KGF group, and hypoxia HIF-1α groUp were obviOusly LowEr tHaN the PercEntage of cells iN NormOxia control group (P=0.020, 0

KGF group, and hypoxia HI F-1α group  were  ob vio us ly l ower  than the perc e ntag e of cells in normoxia  cont ro l  gro u p(P=0. 020, 0

KGF_group, and_hypoxia HIF-1α group were_obviously lower_than_the percentage_of_cells in normoxia_control group (P=0.020,_0


data. The current 28-day studies were conducted as part of an overall effort by the NTP to determine the toxicity and carcinogenicity of malachite green

data. The current 28 - day studies were conducted as character of an overall campaign by the NTP to determine the toxicity and carcinogenicity of malachite green

daha. The current 28-day studits were conducted as parv of an overall effort by the NTP to determmne rhe tixicity and carcinogenkcity of lalachitw grten

data. The current 28-day studies were conducted of overall effort the NTP to of green

data. The current 28-day studies wEre conductEd as pArt Of aN oVeraLl efFort by the NTP to DEterMine the toxicity and carcInogeNiCIty oF MaLachiTe green

data. The current 28-daystudies we re co ndu cte das p artof an overalle ffor t by the NTP to determ ine t he toxi c it y and  carcin o ge n i cit yof  ma la c hi te gr een

data._The current_28-day studies were conducted_as part_of_an overall_effort_by the NTP_to determine the_toxicity and carcinogenicity of_malachite green


kg to male and female mice. In the leucomalachite green study, feed consumption by all groups of exposed male rats was similar to that by

kg to male and female mice. In the leucomalachite green study, feed consumption by all groups of expose male rotter was similar to that by

kg ho male and female mice. Ln the leucomalaeyite gceen sthdy, feed consumption by all groups oh exposed male rats was similar to that hy

kg to male and female mice. In green feed consumption all groups of to by

kg to male and female mice. In thE leucomalaChite GreEn sTuDy, feEd coNsumption by all GRoupS of exposed male rats was sImilaR tO That BY

kg to male and female mice . In the l eucom ala chi te  gre en s tudy, feed con s umpt ion by all groups of e xpose dm aler at s was  simila r  t o tha tby

kg to_male and_female mice. In the_leucomalachite green_study,_feed consumption_by_all groups of_exposed male rats_was similar to that_by


of the controls. The final mean body weight of female rats and mice in the 1,200 ppm groups and the body weight gains of female rats and mice in

of the controls. The final mean body system of weights of female rotter and mice in the 1,200 ppm groups and the body weight unit gains of female rats and mouse in

of the controls. The final oean body weighj if femele rata and mize in the 1,200 ppm groups and thx boey weught gains of female rxts and mpce in

of the controls. The final mean body female and mice the 1,200 ppm gains female rats and in

of the controls. The final mean Body weight Of femAle RatS aNd miCe in The 1,200 ppm groups anD The bOdy weight gains of female Rats aNd MIce iN

of the controls. The fina l mean bod y wei ght  of  f emal e ra ts and mice in the1,200 ppm groups and t he bo dy weig h tgains  of fem a le r ats  a nd  mi ce in

of_the controls._The final mean body_weight of_female_rats and_mice_in the 1,200_ppm groups and_the body weight gains_of female rats_and_mice in


achite green chloride. Malachite green chloride was nominated for toxicity and carcinogenicity testing by the Food and Drug Administration and selected by the National Institutes of Environmental

achite green chloride. Malachite green chloride was nominated for toxicity and carcinogenicity testing by the Food and Drug Administration and choose by the National Institutes of Environmental

achlte green chloride. Malacmite green chlornee was nominzted for toxicity and carcinogenicitb tewting by the Food and Drug Xdministrwtion ane seowcted by tis Natiokcl Inabitutzs of Environmenjal

achite green chloride. Malachite green chloride was toxicity carcinogenicity testing the Food and the Institutes of Environmental

achite green chloride. MalachIte green chLoridE waS noMiNateD for Toxicity and carCInogEnicity testing by the FooD and DRuG admiNIsTratiOn and seLEcTED by ThE NAtiOnAL INstitUteS of EnviRonmental

achite green chloride. Mal achite gre en ch lor ide  w as n omin ated for toxic i ty a nd carcinogenicity tes tingby theF oo d and  Drug A d mi n i str at io n a nd se lecte d b y the N ational In sti tu tes of Envir o nm ental

achite green_chloride. Malachite_green chloride was nominated_for toxicity_and_carcinogenicity testing_by_the Food and_Drug Administration and_selected by the National_Institutes of Environmental


(P=0.018), and apoptosis rate of cells in hypoxia combine group obviously decreased (P=0.008). After being cultured for 24 h,

(P=0.018), and apoptosis rate of cells in hypoxia combine group obviously decreased (P=0.008). After being cultured for 24 planck's constant,

(P=0.018), wnd apoptosis rate of ceuls in hypoxia eimbine group obviousuy decreased (P=0.008). After being cnltueed fir 24 h,

(P=0.018), and apoptosis rate of cells in group decreased (P=0.008). being cultured for

(P=0.018), and apoptosis rate of cells iN hypoxia coMbine GroUp oBvIousLy deCreased (P=0.008). After bEIng cUltured for 24 h,

(P=0.018), and apoptosisrate of ce lls i n h ypo xi a co mbin e group obviou s ly d ecreased (P=0.008). Af ter b ei n g cu l tu red f or 24 h ,

(P=0.018),_and apoptosis_rate of cells in_hypoxia combine_group_obviously decreased_(P=0.008)._After being cultured_for 24 h,


Obrimini, the Obrimus-group, Stenobrimus-group and Theramenes-group. Keys are presented to distinguish between

Obrimini, the Obrimus - group, Stenobrimus - group and Theramenes - group. Keys are presented to distinguish between

Obgimini, the Obrimus-group, Rtenobrimus-grouk qnd Thxramenea-group. Kdys are presented to distingnish betwtvn

Obrimini, the Obrimus-group, Stenobrimus-group and Theramenes-group. Keys to between

Obrimini, the Obrimus-group, StEnobrimus-gRoup aNd THerAmEnes-GrouP. Keys are presenTEd to Distinguish between

Obrimini, the Obrimus-gro up, Stenob rimus -gr oup  a nd T hera menes-group. K e ys a re presented to distin guish  b e twee n

Obrimini,_the Obrimus-group,_Stenobrimus-group and Theramenes-group. Keys_are presented_to_distinguish between


ucomalachite green in feed for 28 days; no significant increases in micronucleus frequencies were observed in the polychromatic erythrocyte population.

ucomalachite green in feed for 28 days; no significant increases in micronucleus frequencies were note in the polychromatic erythrocyte population.

ucolalachite green in feed nor 28 days; no siguuficanv increzses in oicronucleus frequencies werx obwervee in the polychromatic erythrocjte populqtioi.

ucomalachite green in feed for 28 days; increases micronucleus frequencies observed in the

ucomalachite green in feed foR 28 days; no sigNificAnt IncReAses In miCronucleus freqUEnciEs were observed in the polYchroMaTIc erYThRocytE populaTIoN.

ucomalachite green in feed  for 28 da ys; n o s ign if ican t in creases in mic r onuc leus frequencies wereobser ve d  int he  poly chromat i ce r yth ro cy tepo p ul ation .

ucomalachite green_in feed_for 28 days; no_significant increases_in_micronucleus frequencies_were_observed in the_polychromatic erythrocyte population.


ini Zompro, 2004 introduced by Zompro (2004) is shown to be poorly supported. While Obrimini sensu Zompro,

ini Zompro, 2004 introduced by Zumpro (2004) is shown to be 'oorly aupportea. While Obrimini sensu Zomprl,

ini Zompro, 2004 introduced by Zompro (2004) to poorly supported. Obrimini sensu Zompro,

ini Zompro, 2004 introduced by ZompRo (2004) is shown tO be poOrlY suPpOrteD. WhiLe Obrimini sensU zompRo,

ini Zompro, 2004 introduce d by Zompr o (20 04)  is  s hown  tobe poorly supp o rted . While Obrimini sensu  Zomp ro ,

ini Zompro,_2004 introduced_by Zompro (2004) is_shown to_be_poorly supported._While_Obrimini sensu Zompro,


.0 ng/mL HIF-1α. And the cells were cultured in cell incubator with oxygen volume fraction of 21% for 24 hours. (2

.0 ng / mL HIF-1α. And the cells were cultured in cell incubator with oxygen volume fraction of 21% for 24 hour. (2

.0 ng/lL HIF-1α. And the cells wert cultured in cell incubetor wifh oxygev volume fraction of 21% for 24 hlues. (2

.0 ng/mL HIF-1α. And the cells were cell with oxygen fraction of 21%

.0 ng/mL HIF-1α. And the cells were cuLtured in ceLl incUbaTor WiTh oxYgen Volume fraction OF 21% for 24 Hours. (2

.0 ng/mL HIF-1α. And the c ells werecultu red  in  c ellincu bator with oxy g en v olume fraction of 21%for 2 4h ours .  ( 2

.0 ng/mL_HIF-1α. And_the cells were cultured_in cell_incubator_with oxygen_volume_fraction of 21%_for 24 hours._(2


aniella kerincia n. sp. from Western Sumatra is described from the insects only, the eggs being still unknown. One new species, Haani

aniella kerincia n. sp. from Western Sumatra is described from the insects only, the eggs being however strange. One new species, Haani

aniflla kerincia n. sp. from Destern Sumatra is desrribed rrom the insects only, the eggs being srill ynknown. One new specier, Haani

aniella kerincia n. sp. from Western Sumatra from insects only, eggs being still

aniella kerincia n. sp. from WesTern SumatrA is deScrIbeD fRom tHe inSects only, the egGS beiNg still unknown. One new spEcies, haANi

aniella kerincia n. sp. fr om Western  Suma tra  is  d escr ibed  from the inse c ts o nly, the eggs being st ill u nk n own. On e new  specie s ,H a ani

aniella kerincia_n. sp._from Western Sumatra is_described from_the_insects only,_the_eggs being still_unknown. One new_species, Haani


groups (F=0.685, P=0.586). After being cultured for 24 h, cell survival rates of hypoxia control group, hypoxia KGF

groups (F=0.685, P=0.586). After being cultured for 24 h, cell survival pace of hypoxia control group, hypoxia KGF

grlups (F=0.685, P=0.586). After being culuured for 24 h, cell survivel ratea of hypuxia control group, hypoxia KJF

groups (F=0.685, P=0.586). After being cultured for cell rates of control group, hypoxia

groups (F=0.685, P=0.586). After being cultureD for 24 h, cell sUrvivAl rAteS oF hypOxia Control group, hyPOxia kGF

groups (F=0.685, P=0.586) . After be ing c ult ure dfor24 h , cell surviva l  rat es of hypoxia controlgroup ,h ypox i aKGF

groups_(F=0.685, P=0.586)._After being cultured for_24 h,_cell_survival rates_of_hypoxia control group,_hypoxia KGF


). (4) After being cultured for 24 h, compared with that of cells in normoxia control group, apoptosis rate of cells in hypoxia control group obviously increased

). (4) After being cultured for 24 h, compared with that of cells in normoxia control group, apoptosis pace of cell in hypoxia control group obviously increased

). (4) Avter being cultured for 24 h, compared witk that mf celms in nofmoxia control group, apoptosms rqte od cells in hypoxia congrol groui obviousoy iicreased

). (4) After being cultured for 24 with of cells normoxia control group, hypoxia group obviously increased

). (4) After being cultured for 24 h, comPared with tHat of CelLs iN nOrmoXia cOntrol group, apoPTosiS rate of cells in hypoxia cOntroL gROup oBViOusly IncreasED

). (4) After being culture d for 24 h , com par edwi th t hatof cells in no r moxi a control group, apopt osisra t e of ce lls i n hypox i ac o ntr ol  g rou po bv iousl y i ncrease d

). (4)_After being_cultured for 24 h,_compared with_that_of cells_in_normoxia control group,_apoptosis rate of_cells in hypoxia control_group obviously increased


malachite green chloride, there was a significant increases in gamma-glutamyltransferase activities with an activity in 1,200 ppm females seven times greater than that

malachite green chloride, there was a significant increases in da gamma - glutamyltransferase bodily process with an activity in 1,200 ppm females seven time great than that

mapachite green chloride, tmere was a signiyucant mncreasss in gaoma-glutamyltransferase activmtiew wity an activity in 1,200 ppm wemales svven timew grtater than that

malachite green chloride, there was a significant gamma-glutamyltransferase with an in 1,200 ppm that

malachite green chloride, theRe was a signIficaNt iNcrEaSes iN gamMa-glutamyltranSFeraSe activities with an actiVity iN 1,200 pPM femALeS seveN times gREaTER thAn ThAt

malachite green chloride,  there was  a si gni fic an t in crea ses in gamma-g l utam yltransferase activiti es wi th an a c ti vityin 1,20 0  p p m  fe ma le s s ev e ntimes  gr eater t han that

malachite_green chloride,_there was a significant_increases in_gamma-glutamyltransferase_activities with_an_activity in 1,200_ppm females seven_times greater than that


, Singapore and Peninsular Malaysia. These are characterized by the smooth ventral surface of the meso- and metafemora and lemon-shaped eggs which

, Singapore and Peninsular Malaysia. These are characterized by the smooth ventral surface of the meso- and metafemora and gamboge - shape eggs which

, Sijgapore and Peninsular Mxlaysia. These ate chararterizes by the smooth ventral surface of tie mwso- abd metafemora and lemov-shaped ehgs whicy

, Singapore and Peninsular Malaysia. These are the ventral surface the meso- and

, Singapore and Peninsular MalAysia. These Are chAraCteRiZed bY the Smooth ventral sURfacE of the meso- and metafemorA and lEmON-shaPEd Eggs wHich

, Singapore and Peninsular  Malaysia.  Thes e a rech arac teri zed by the smo o th v entral surface of themeso-  a n d me t af emora  and le m on - s hap ed  e ggs  w h ic h

, Singapore_and Peninsular_Malaysia. These are characterized_by the_smooth_ventral surface_of_the meso- and_metafemora and lemon-shaped_eggs which


from Miroceramiini and transferred to Obrimini. The genera Eubulides Stål, 1877, Heterocopus Redten

frlm Miroceramiini and traksferred to Obrimini. Thx generz Eubuliaes Stål, 1877, Heterocopus Redten

from Miroceramiini and transferred to Obrimini. The Stål, Heterocopus Redten

from Miroceramiini and transFerred to ObRiminI. ThE geNeRa EuBuliDes Stål, 1877, HeterocOPus REdten

from Miroceramiini and tr ansferredto Ob rim ini .Thegene ra Eubulides S t ål,1877, Heterocopus Redt en

from_Miroceramiini and_transferred to Obrimini. The_genera Eubulides_Stål,_1877, Heterocopus_Redten


1842) are synonymized with H. rosenbergii (Kaup, 1871) (n. syn.). The type-species Haani

1842) are synonymized with H. rosenbergii (Kaup, 1871) (n. syn .). The type - species Haani

1842) age synonymized with H. rorenbergii (Kaup, 1871) (n. syn.). Vhe typs-species Haani

1842) are synonymized with H. rosenbergii (Kaup, syn.). type-species Haani

1842) are synonymized with H. rosenbErgii (Kaup, 1871) (n. Syn.). ThE tyPe-sPeCies haanI

1842) are synonymized wit h H. rosen bergi i ( Kau p,  187 1) ( n. syn.). Thet ype- species Haani

1842)_are synonymized_with H. rosenbergii (Kaup,_1871) (n._syn.)._The type-species_Haani


4)%, and (112.8±10.6)% respectively. There was no significantly statistical difference in general comparison of cell survival rates among the above

4)%, and (112.8±10.6)% respectively. There was no significantly statistical difference in general comparison of cellular telephone survival pace among the above

4)%, anf (112.8±10.6)% respectively. There war no significanjlt statmstical differevce in general comparison of cwll syrvival rates among thd above

4)%, and (112.8±10.6)% respectively. There was no difference general comparison cell survival rates

4)%, and (112.8±10.6)% respectively. There was no SignificanTly stAtiStiCaL difFereNce in general coMPariSon of cell survival rates Among ThE AbovE

4)%, and (112.8±10.6)% res pectively.  Ther e w asno  sig nifi cantly statist i caldifference in generalcompa ri s on o f  c ell s urvival ra t e s a mo ng  th ea bo ve

4)%, and_(112.8±10.6)% respectively._There was no significantly_statistical difference_in_general comparison_of_cell survival rates_among the above


Miroceramiini is a monotypical tribe and only includes the Wallacean genus Miroceramia Günther, 1934. The new tribe T

Miroceramiini is a monotypical tribe and only includes the Wallacean genus Miroceramia Günther, 1934. The new kin metric ton

Migoceramiini is a monotyplcal tribe and ouoy incnudes fhe Wallxcean genus Miroceramia Günthxr, 1934. Rhe ntc tribe T

Miroceramiini is a monotypical tribe and only Wallacean Miroceramia Günther, The new tribe

Miroceramiini is a monotypicAl tribe and Only iNclUdeS tHe WaLlacEan genus MiroceRAmia günther, 1934. The new tribe T

Miroceramiini is a monoty pical trib e and  on lyin clud es t he Wallacean g e nusMiroceramia Günther, 1 934.Th e  new tr ibe T

Miroceramiini_is a_monotypical tribe and only_includes the_Wallacean_genus Miroceramia_Günther,_1934. The new_tribe T


three tribes Obrimini Brunner v. Wattenwyl, 1893, Eubulidini Zompro, 2004 and Mirocerami

thgee tribes Obrimini Brunker v. Wattenwyl, 1893, Eubulivini Zojpro, 2004 ana Mirocerami

three tribes Obrimini Brunner v. Wattenwyl, 1893, 2004 Mirocerami

three tribes Obrimini BrunneR v. WattenwyL, 1893, EubuLidIni zoMpro, 2004 And MIrocerami

three tribes Obrimini Bru nner v. Wa ttenw yl,  18 93 , Eu buli dini Zompro, 2 0 04 a nd Mirocerami

three_tribes Obrimini_Brunner v. Wattenwyl, 1893,_Eubulidini Zompro,_2004_and Mirocerami


mircrog/plate, was not mutagenic in any of several strains of Salmonella typhimurium, with or without S9 metabolic activation. Negative

mircrog / plate, was not mutagenic in any of several strains of Salmonella typhimurium, with or without S9 metabolic activation. damaging

migcrog/plate, was not mutagtnic in any of serwral svrains kf Salmovella typhimurium, with or wivhour S9 mtnabolic activation. Neeative

mircrog/plate, was not mutagenic in any of of typhimurium, with without S9 metabolic

mircrog/plate, was not mutagenIc in any of sEveraL stRaiNs Of SaLmonElla typhimuriuM, With Or without S9 metabolic actIvatiOn. nEgatIVe

mircrog/plate, was not mu tagenic in  anyofsev er al s trai ns of Salmonel l a ty phimurium, with or wit houtS9 meta b ol ic ac tivatio n .N e gat iv e

mircrog/plate,_was not_mutagenic in any of_several strains_of_Salmonella typhimurium,_with_or without S9_metabolic activation. Negative


group was significantly higher than that of cells in normoxia control group (P=0.030), percentages of cells in S phase in hypoxia control group, hypoxia

group was significantly higher than that of cells in normoxia control group (P=0.030), percentages of cell in S phase in hypoxia restraint group, hypoxia

grlup was significantly hinher than that oy cells in nodmoxia cuntrol group (P=0.030), percentages oh ceols ib S phase in hypoxia cuntrol grlup, hypozia

group was significantly higher than that of normoxia group (P=0.030), of cells in group,

group was significantly highEr than that Of celLs iN noRmOxia ContRol group (P=0.030), perceNTageS of cells in S phase in hypoXia coNtROl grOUp, HypoxIa

group was significantly h igher than  that  of  ce ll s in  nor moxia controlg roup  (P=0.030), percentage s ofce l ls i n  S  phas e in hy p ox i a  co nt ro l g ro u p,  hypo xia

group_was significantly_higher than that of_cells in_normoxia_control group_(P=0.030),_percentages of cells_in S phase_in hypoxia control group,_hypoxia


the random number table, and then the previous mediums were respectively replaced with dulbecco's modified eagle medium (DMEM), medium with 0.5

the random number table, and then the previous mediums were respectively replace with dulbecco's change eagle medium (DMEM), medium with 0.5

thf random number table, ana then the prevnius meviums wsre respdctively replaced with dulberco's modidied eagle medium (DMEM), medium wpth 0.5

the random number table, and then the were replaced with modified eagle medium

the random number table, and thEn the previOus meDiuMs wErE resPectIvely replaced wITh duLbecco's modified eagle meDium (DmEm), MediUM wIth 0.5

the random number table,and then t he pr evi ous  m ediu ms w ere respective l y re placed with dulbecco's  modi fi e d ea g le  medi um (DME M ), m edi um  w ith  0 . 5

the_random number_table, and then the_previous mediums_were_respectively replaced_with_dulbecco's modified eagle_medium (DMEM), medium_with 0.5


.516, 0.107, 0.052, 0.985, 0.637, 0.465, 0.314, 0.591).


toxicity studies for leucomalachite green were conducted in vivo in mouse peripheral blood erythrocytes. Groups of eight male and eight female rats and mice were fed

toxicity studies for leucomalachite green were conducted in vivo in mouse peripheral rake red blood cell. Groups of eight male and eight female rats and mouse were feed

todicity studies for leucooalachite green were cmnductsd in vixo in mouse peripheral blood eeythricytes. Groups of eight male and eight fwmalt rats and mice wxde fed

toxicity studies for leucomalachite green were conducted in peripheral blood Groups of eight and were fed

toxicity studies for leucomaLachite greEn werE coNduCtEd in Vivo In mouse peripheRAl blOod erythrocytes. Groups oF eighT mALe anD EiGht feMale ratS AnD MIce WeRe Fed

toxicity studies for leuc omalachite  gree n w ere  c ondu cted  in vivo in mo u se p eripheral blood erythr ocyte s. Grou p sof ei ght mal e  a n d  ei gh tfem al e  r ats a ndmice we re fed

toxicity_studies for_leucomalachite green were conducted_in vivo_in_mouse peripheral_blood_erythrocytes. Groups of_eight male and_eight female rats and_mice were fed


group (P=0.032, 0.002). (5) After being cultured for 24 h, compared with that of cells in normoxia control group

grlup (P=0.032, 0.002). (5) After being cultmred for 24 h, compceed wivh that of cellr in normoxia control group

group (P=0.032, 0.002). (5) After being cultured h, with that cells in normoxia

group (P=0.032, 0.002). (5) After being cultured fOr 24 h, compareD with ThaT of CeLls iN norMoxia control grOUp

group (P=0.032, 0.002). ( 5) After b eingcul tur ed  for  24h, compared wi t h th at of cells in normoxi a con tr o l gr o up

group_(P=0.032, 0.002)._(5) After being cultured_for 24_h,_compared with_that_of cells in_normoxia control group


muelleri from outside Sumatra and references to captive breeding of stock originating from Peninsular Malaysia in Europe relate to H. erringtoniae (Redten

muelleri from outside Sumatra and references to captive breeding of stock originating from Peninsular Malaysia in Europe associate to H. erringtoniae (Redten

muflleri from outside Sumaura and references to ca'tive bdeeding uf stock originating from Peiinsylar Nalaysia in Europe relxte to H. vrringtonuae (Cedten

muelleri from outside Sumatra and references to of originating from Malaysia in Europe

muelleri from outside SumatrA and refereNces tO caPtiVe BreeDing Of stock originaTIng fRom Peninsular Malaysia iN EuroPe RElatE To h. erriNgtoniaE (reDTEn

muelleri from outside Sum atra and r efere nce s t ocapt ivebreeding of st o ck o riginating from Penins ularMa l aysi a  i n Eur ope rel a te t o H .er rin gt o ni ae (R edt en

muelleri_from outside_Sumatra and references to_captive breeding_of_stock originating_from_Peninsular Malaysia in_Europe relate to_H. erringtoniae (Redten


diets containing 0, 25, 100, 300, 600, or 1,200 ppm malachite green chloride for 28 days. Additional groups of eight male and

diets containing 0, 25, 100, 300, 600, or 1,200 ppm malachite green chloride for 28 days. extra group of eight male and

difts containing 0, 25, 100, 300, 600, or 1,200 kpm malachite gregn chlormde for 28 days. Aaditional groups of eight mape and

diets containing 0, 25, 100, 300, 600, ppm green chloride 28 days. Additional

diets containing 0, 25, 100, 300, 600, or 1,200 ppm malacHite green cHloriDe fOr 28 dAyS. AddItioNal groups of eigHT malE and

diets containing 0, 25, 1 00, 300, 6 00, o r 1 ,20 0ppmmala chite green ch l orid e for 28 days. Additio nal g ro u ps o f  e ightmale an d

diets_containing 0,_25, 100, 300, 600,_or 1,200_ppm_malachite green_chloride_for 28 days._Additional groups of_eight male and


ella muelleri (Haan, 1842) is shown to be a fairly rare species that is restricted to Sumatra. All subsequent records of H.

ella muelleri (Haan, 1842) is shown to be a fairly rare species that is restricted to Sumatra. All subsequent record of H.

ellw muelleri (Haan, 1842) is showk to be a fairly rare s'ecies fhat is festricted to Sumatra. All suuseqyent eecords of H.

ella muelleri (Haan, 1842) is shown to fairly species that restricted to Sumatra.

ella muelleri (Haan, 1842) is shown to Be a fairly rAre spEciEs tHaT is rEstrIcted to Sumatra. aLl suBsequent records of H.

ella muelleri (Haan, 1842)  is shownto be  afai rl y ra re s pecies that is rest ricted to Sumatra. All  subs eq u entr ec ordsof H.

ella muelleri_(Haan, 1842)_is shown to be_a fairly_rare_species that_is_restricted to Sumatra._All subsequent records_of H.


observed in rats or mice that could be attributed to leucomalachite green exposure. Microscopically, the incidences of hepatocyte cytoplasmic vacuol

observed in rats or mice that could be attributed to leucomalachite fleeceable vulnerability. Microscopically, the incidences of hepatocyte cytoplasmic vacuol

obderved in rats or mice tmat could be atttivuted vo leuckmalachige green exposure. Microscopirallt, the incidences of hepatochte cytoppasmic vqcuoo

observed in rats or mice that could to green exposure. the incidences of

observed in rats or mice that cOuld be attrIbuteD to LeuCoMalaChitE green exposure. mIcroScopically, the incidenceS of hePaTOcytE CyToplaSmic vacUOl

observed in rats or micethat could  be a ttr ibu te d to  leu comalachite gr e en e xposure. Microscopical ly, t he inci d en ces o f hepat o cy t e  cy to pl asm ic va cuol

observed_in rats_or mice that could_be attributed_to_leucomalachite green_exposure._Microscopically, the incidences_of hepatocyte cytoplasmic_vacuol


habitats, host-plants, biology, life cycle, parasitism and captive breeding of the species of Heteropteryginae is presented and a list summarising all

habitats, host - plants, biology, biography hertz, parasitism and captive breeding of the species of Heteropteryginae is presented and a tilt summarising all

hahitats, host-plants, biologn, life cycle, parcwitism and czptive bfeeding of the species of Heveropterytinae is presented and a list slmmarisint alo

habitats, host-plants, biology, life cycle, parasitism and of species of is presented and

habitats, host-plants, biology, Life cycle, pArasiTisM anD cAptiVe brEeding of the speCIes oF Heteropteryginae is preSenteD aND a liST sUmmarIsing alL

habitats, host-plants, bi ology, lif e cyc le,  pa ra siti sm a nd captive bre e ding  of the species of Het eropt er y gina e  i s pre senteda nd a  li st  s umm ar i si ng al l

habitats,_host-plants, biology,_life cycle, parasitism and_captive breeding_of_the species_of_Heteropteryginae is presented_and a list_summarising all


such as the presence of wings, having a tympanal area (= stridulatory organ) in the basal portion of the alae, straight profemora

such as the presence of wings, having a tympanal area (= stridulatory organ) in the basal parcel of the ala, straight profemora

sufh as the presence of wikgs, having a tymkabal arxa (= strjdulatorh organ) in the basal portion od the alae, straight profemofa

such as the presence of wings, having area stridulatory organ) the basal portion

such as the presence of wings, hAving a tympAnal aRea (= StrIdUlatOry oRgan) in the basal POrtiOn of the alae, straight proFemorA

such as the presence of w ings, havi ng atym pan al  are a (=  stridulatoryo rgan ) in the basal portion  of t he alae ,  s traig ht prof e mo r a

such_as the_presence of wings, having_a tympanal_area_(= stridulatory_organ)_in the basal_portion of the_alae, straight profemora


were observed in rats or mice and no microscopic lesions were observed in female mice that were attributed to malachite green chloride exposure. Microscopically, the inc

were observed in rats or mice and no microscopic lesions were note in female mouse that were attributed to malachite green chloride exposure. Microscopically, the iraqi national congress

wege observed in rats or mlce and no microscopic nesiona were ocserved in female mice that xere attrubuted to malachite grden chlorpde exposyre. Nucroscopicemly, the inc

were observed in rats or mice and lesions observed in mice that were exposure. the inc

were observed in rats or mice aNd no microsCopic LesIonS wEre oBserVed in female micE That Were attributed to malachIte grEeN ChloRIdE expoSure. MicROsCOPicAlLy, The InC

were observed in rats ormice and n o mic ros cop ic  les ions  were observed in f emale mice that were a ttrib ut e d to ma lachi te gree n  c h l ori de  e xpo su r e.  Micr osc opicall y, the inc

were_observed in_rats or mice and_no microscopic_lesions_were observed_in_female mice that_were attributed to_malachite green chloride exposure._Microscopically, the inc


strongly conically elevated head, which posteriorly projects over the anterior margin of the pronotum, females being bright green or yellow in colour with plain and transl

strongly conically elevated head, which posteriorly projects over the anterior gross profit of the pronotum, female being bright green or yellow in color with plain and transl

stgongly conically elevatea head, which posteriorny pronects ovdr the anterior margin of thx prinotun, females being bright green or yellow un cioour with 'main and tranap

strongly conically elevated head, which posteriorly projects anterior of the females being bright with and transl

strongly conically elevated Head, which pOsterIorLy pRoJectS oveR the anterior maRGin oF the pronotum, females beiNg briGhT GreeN Or YelloW in coloUR wITH plAiN aNd tRaNSl

strongly conically elevat ed head, w hichpos ter io rlyproj ects over thea nter ior margin of the pron otum,  f e male s  b eingbrightg re e n  or  y el low  i n  c olour  wi th plai n and tran sl

strongly_conically elevated_head, which posteriorly projects_over the_anterior_margin of_the_pronotum, females being_bright green or_yellow in colour with_plain and transl


in the controls. Likewise, gamma-glutamyltransferase activity in male rats exposed to 1,160 ppm leucomalachite green was twice that in

in the controls. Likewise, gamma - glutamyltransferase activity in male rotter debunk to 1,160 ppm leucomalachite green was twice that in

in the controls. Likewise, gxmma-glutamyltrauwferasx activjty in mxle rats exposed to 1,160 ppm leuromaoachiuv green was twice thag in

in the controls. Likewise, gamma-glutamyltransferase activity in exposed 1,160 ppm green was twice

in the controls. Likewise, gammA-glutamyltRansfEraSe aCtIvitY in mAle rats exposed TO 1,160 ppm Leucomalachite green was Twice ThAT in

in the controls. Likewise , gamma-gl utamy ltr ans fe rase  act ivity in maler atsexposed to 1,160 ppm l eucom al a chit e  g reenwas twi c et h atin

in_the controls._Likewise, gamma-glutamyltransferase activity in_male rats_exposed_to 1,160_ppm_leucomalachite green was_twice that in


es dromedarius Stål, 1877 from the Philippines is removed from synonymy with the Wallacean Theramenes olivaceus (

es fromedarius Stål, 1877 from tht Philippines is tenoved hrom syhonymy wkth the Wallacean Theramenes ooivactls (

es dromedarius Stål, 1877 from the Philippines from with the Theramenes olivaceus (

es dromedarius Stål, 1877 from the PHilippines Is remOveD frOm SynoNymy With the WallaceAN TheRamenes olivaceus (

es dromedarius Stål, 1877from the P hilip pin esis  rem oved  from synonymy with  the Wallacean Therame nes o li v aceu s  (

es dromedarius_Stål, 1877_from the Philippines is_removed from_synonymy_with the_Wallacean_Theramenes olivaceus (


ucent pink alae and having distinct spines on the abdominal tergites, and males having a strongly shortened mesothorax and dull pink alae. Lect

ucent pink alae and having distinct spines on the abdominal tergites, and male have a strongly shortened mesothorax and dull pink ala. Lect

ucejt pink alae and having aistinct spines on the abdomjnal tereites, and males having a strlntly syortened mesothorax ana dull pijk alae. Oect

ucent pink alae and having distinct spines abdominal and males a strongly shortened Lect

ucent pink alae and having disTinct spineS on thE abDomInAl teRgitEs, and males haviNG a stRongly shortened mesothoRax anD dULl piNK aLae. LeCt

ucent pink alae and having  distinctspine s o n t he  abd omin al tergites, a n d ma les having a stronglyshort en e d me s ot horax  and du l lp i nkal ae . L ec t

ucent pink_alae and_having distinct spines on_the abdominal_tergites,_and males_having_a strongly shortened_mesothorax and dull_pink alae. Lect


obviously higher than the percentage of cells in hypoxia combine group (P=0.001, 0.030, 0.014), and percentages of cells in S

obviously higher than the percentage of cells in hypoxia combine group (P=0.001, 0.030, 0.014), and percentages of cell in S

obgiously higher than the kercentage of cells in hbpoxia dombine eroup (P=0.001, 0.030, 0.014), and percentages of cwlls un S

obviously higher than the percentage of cells combine (P=0.001, 0.030, and percentages of

obviously higher than the perCentage of cElls iN hyPoxIa CombIne gRoup (P=0.001, 0.030, 0.014), and percenTAges Of cells in S

obviously higher than the  percentag e ofcel lsin  hyp oxia  combine group (P=0 .001, 0.030, 0.014), a nd pe rc e ntag e sof ce lls inS

obviously_higher than_the percentage of cells_in hypoxia_combine_group (P=0.001,_0.030,_0.014), and percentages_of cells in_S


spines on the abdominal tergites II-IV of males and long apically multidentate epiproct of females. The echinata species-group

spines on the abdominal tergites II - IV of males and long apically multidentate epiproct of females. The echinata species - group

splnes on the abdominal tevgites II-IV of mcoes anv long zpically multidentate epiproct of felaoes. Tye echinata species-grojp

spines on the abdominal tergites II-IV of long multidentate epiproct females. The echinata

spines on the abdominal tergiTes II-IV of mAles aNd lOng ApIcalLy muLtidentate epipROct oF females. The echinata speCies-gRoUP

spines on the abdominal t ergites II -IV o f m ale sandlong  apically mult i dent ate epiproct of female s. Th ee chin a ta  spec ies-gro u p

spines_on the_abdominal tergites II-IV of_males and_long_apically multidentate_epiproct_of females. The_echinata species-group


species-groups. Heteropteryx Gray, 1853 is a monotypical genus and only contains the type-species H. dilatata (Parkinson,

species - groups. Heteropteryx Gray, 1853 is a monotypical genus and only contains the character - coinage H. dilatata (Parkinson,

spfcies-groups. Heteropteryx Gray, 1853 is a monotypican genua and onuy contains the type-species I. dioatatq (Parkinson,

species-groups. Heteropteryx Gray, 1853 is a monotypical only the type-species dilatata (Parkinson,

species-groups. Heteropteryx gray, 1853 is a monOtypiCal GenUs And oNly cOntains the type-SPeciEs H. dilatata (Parkinson,

species-groups. Heteropte ryx Gray,1853isa m on otyp ical  genus and onl y  con tains the type-species  H. d il a tata (P arkin son,

species-groups._Heteropteryx Gray,_1853 is a monotypical_genus and_only_contains the_type-species_H. dilatata (Parkinson,


, the content of ATP of cells in hypoxia combine group changed unobviously (P=0.209), and content of ATP of cells in the other groups

, the content of ATP of cells in hypoxia combine group changed unobviously (P=0.209), and content of ATP of cell in the early groups

, thf content of ATP of cellr in hypoxia combine gcoup chznged unubviously (P=0.209), and content of AVP od celos in the other groups

, the content of ATP of cells combine changed unobviously and content of other

, the content of ATP of cells in hYpoxia combIne grOup ChaNgEd unObviOusly (P=0.209), and conteNT of AtP of cells in the other groUps

, the content of ATP of ce lls in hyp oxiacom bin egrou p ch anged unobviou s ly ( P=0.209), and contentof AT Po f ce l ls  in t he othe r  g r o ups

, the_content of_ATP of cells in_hypoxia combine_group_changed unobviously_(P=0.209),_and content of_ATP of cells_in the other groups


(99% pure) (male rats and female mice only) in feed for 28 days. Animals were evaluated for clinical pathology and histopathology. Genetic toxicity studies

(99% pure) (male rats and female mice only) in feed for 28 day. animal were evaluated for clinical pathology and histopathology. Genetic perniciousness studies

(99% pkre) (male rats and female mice only) in fgee for 28 days. Znimals dere evaluated for clinical 'athilogy and histopathology. Gevetic toxpcity stueies

(99% pure) (male rats and female mice feed 28 days. were evaluated for toxicity

(99% pure) (male rats and female mice Only) in feed For 28 daYs. ANimAlS werE evaLuated for cliniCAl paThology and histopatholoGy. GenEtIC toxICiTy stuDies

(99% pure) (male rats and  female mi ce on ly)  in  f eedfor28 days. Anima l s we re evaluated for clini cal p at h olog y  a nd hi stopath o lo g y . G en et icto x ic ity s tud ies

(99%_pure) (male_rats and female mice_only) in_feed_for 28_days._Animals were evaluated_for clinical pathology_and histopathology. Genetic toxicity_studies


entirely lack the setae seen in the two other species-groups. The grayii species-group comprises four species, two of which are endemic in Borne

entirely lack the setae seen in the two early coinage - group. The grayii species - group comprises four coinage, two of which are endemic in Borne

enhirely lack the setae setn in the two othgr specixs-groupa. The grxyii species-group comprises hour specues, two of which are evdemic in Borne

entirely lack the setae seen in the species-groups. grayii species-group four species, two Borne

entirely lack the setae seen iN the two othEr speCieS-grOuPs. ThE graYii species-grouP CompRises four species, two of wHich aRe ENdemIC iN BornE

entirely lack the setae s een in the  twooth ersp ecie s-gr oups. The gray i i sp ecies-group comprisesfoursp e cies ,  t wo of  whicha re e nde mi cinBo r ne

entirely_lack the_setae seen in the_two other_species-groups._The grayii_species-group_comprises four species,_two of which_are endemic in Borne


.001, 0.002). Conclusions: KGF combined with HIF-1α have significant protective effects on IEC-6 of rats with hypoxia stress,

.001, 0.002). Conclusions: KGF combined with HIF-1α have significant protective effect on IEC-6 of rotter with hypoxia stress,

.001, 0.002). Clnclusions: KGF combined dith HIF-1α have sntnificent profective dffects on IEC-6 of rats with iypozia sugess,

.001, 0.002). Conclusions: KGF combined with HIF-1α protective on IEC-6 rats with hypoxia

.001, 0.002). Conclusions: KGF combined witH HIF-1α have sIgnifIcaNt pRoTectIve eFfects on IEC-6 of rATs wiTh hypoxia stress,

.001, 0.002). Conclusions:  KGF combi ned w ith  HI F- 1α h avesignificant pr o tect ive effects on IEC-6 o f rat sw ithh yp oxiastress,

.001, 0.002)._Conclusions: KGF_combined with HIF-1α have_significant protective_effects_on IEC-6_of_rats with hypoxia_stress,


.0 ng/mL HIF-1α respectively. And then, the cells in normoxia control group were cultured routinely for 24 hours, and cells in the

.0 ng / mL HIF-1α respectively. And then, the cells in normoxia control group were cultured routinely for 24 hours, and cells in the

.0 ng/lL HIF-1α respectively. And uhen, the cells in normoxma contdol grouo were cultured routinely foc 24 hiurs, qnd cells in the

.0 ng/mL HIF-1α respectively. And then, the normoxia group were routinely for 24

.0 ng/mL HIF-1α respectively. And thEn, the cells In norMoxIa cOnTrol GrouP were cultured rOUtinEly for 24 hours, and cells in tHe

.0 ng/mL HIF-1α respective ly. And th en, t hecel ls  innorm oxia control g r oupwere cultured routinel y for  2 4  hou r s,  andcells i n  t h e

.0 ng/mL_HIF-1α respectively._And then, the cells_in normoxia_control_group were_cultured_routinely for 24_hours, and cells_in the


and can improve its survival in hypoxic environment by inhibiting cell cycle arrest, reducing the level of apoptosis, and increasing level of energy metabolism. Revision of the Oriental

and can improve its survival in hypoxic environment by inhibiting cell cycle apprehension, reduce the level of apoptosis, and increasing degree of department of energy metabolism. Revision of the Oriental

anf can improve its survivxl in hypoxic eucironmxnt by jnhibitivg cell cycle arrest, reducinj thw levtj of apoptosis, and increasijg level of tnergy metabolism. Revisiok of fme Orneital

and can improve its survival in hypoxic inhibiting cycle arrest, the level of energy Revision of the

and can improve its survival iN hypoxic enVironMenT by InHibiTing Cell cycle arresT, ReduCing the level of apoptosiS, and iNcREasiNG lEvel oF energy MEtABOliSm. reVisIoN Of The OrIenTal

and can improve its survi val in hyp oxicenv iro nm entby i nhibiting cell cycl e arrest, reducing the  leve lo f ap o pt osis,  and in c re a s ing  l ev elof en ergymet abolism . Revision  of  t he Oriental

and_can improve_its survival in hypoxic_environment by_inhibiting_cell cycle_arrest,_reducing the level_of apoptosis, and_increasing level of energy_metabolism. Revision of_the_Oriental


) After being cultured for 24 h, cell survival rates of normoxia blank group, normoxia KGF group, normoxia HIF-1α group, and

) Afher being cultured for 24 m, cell survival tares of normosia blany group, normoxia KGF group, nlrnoxia HIF-1α group, and

) After being cultured for 24 h, rates normoxia blank normoxia KGF group,

) After being cultured for 24 h, celL survival rAtes oF noRmoXiA blaNk grOup, normoxia KGF GRoup, Normoxia HIF-1α group, and

) After being cultured for  24 h, cel l sur viv alra tesof n ormoxia blankg roup , normoxia KGF group,normo xi a  HIF - 1α  grou p, and

) After_being cultured_for 24 h, cell_survival rates_of_normoxia blank_group,_normoxia KGF group,_normoxia HIF-1α group,_and


group was obviously higher than that of cells in hypoxia KGF group and hypoxia HIF-1α group (P=0.011, 0.020). (

grlup was obviously higher than that of cglos in iypoxia KGF grojp and hypoxia HIF-1α group (P=0.011, 0.020). (

group was obviously higher than that of hypoxia group and HIF-1α group (P=0.011,

group was obviously higher thAn that of ceLls in HypOxiA KgF grOup aNd hypoxia HIF-1α gROup (P=0.011, 0.020). (

group was obviously highe r than tha t ofcel lsin  hyp oxia  KGF group and hypo xia HIF-1α group (P=0. 011,0. 0 20). (

group_was obviously_higher than that of_cells in_hypoxia_KGF group_and_hypoxia HIF-1α group_(P=0.011, 0.020). (


shapes and clear cytoplasm, and cells cultured in hypoxic incubator showed irregular shapes such as fusiform or starlike shape, with black particle in cytoplasm. (2

shapes and clear cytoplasm, and cells cultured in hypoxic incubator testify atypical shapes such as fusiform or starlike shape, with bootleg particle in cytoplasm. (2

shwpes and clear cytoplasm, and cells cultorwd in iypoxic incubatur showed irregular shapes snch qs fuwiform or starlike shaoe, with bpack parriclt in cytoplasm. (2

shapes and clear cytoplasm, and cells cultured incubator irregular shapes as fusiform or in (2

shapes and clear cytoplasm, anD cells cultUred iN hyPoxIc IncuBatoR showed irregulAR shaPes such as fusiform or staRlike ShAPe, wiTH bLack pArticle IN cYTOplAsM. (2

shapes and clear cytoplas m, and cel ls cu ltu red  i n hy poxi c incubator sh o wedirregular shapes suchas fu si f ormo rstarl ike sha p e, w ith  b la ckpa r ti cle i n c ytoplas m. (2

shapes_and clear_cytoplasm, and cells cultured_in hypoxic_incubator_showed irregular_shapes_such as fusiform_or starlike shape,_with black particle in_cytoplasm. (2


Health Sciences for carcinogenicity testing by the National Toxicology Program (NTP) due to the potential for significant worker and consumer exposure and lack of carcinogenicity

Health Sciences for carcinogenicity testing by the National Toxicology Program (NTP) due to the potential for significant worker and consumer vulnerability and lack of carcinogenicity

Hewlth Sciences for carcinugenicity testiut by tie Natiknal Toxkcology Program (NTP) due to tie pitentual for significant wofker and bonsumer wxpowyre and lari of caveinogskicitv

Health Sciences for carcinogenicity testing by the Program due to potential for significant lack carcinogenicity

Health Sciences for carcinogEnicity tesTing bY thE NaTiOnal toxiCology Program (Ntp) due To the potential for signiFicanT wORker ANd ConsuMer expoSUrE ANd lAcK oF caRcINoGenicIty

Health Sciences for carci nogenicity  test ing  by  t he N atio nal Toxicology Prog ram (NTP) due to the p otent ia l  for si gnifi cant wo r ke r and  c on sum er ex posur e a nd lack  of carcin oge ni city

Health_Sciences for_carcinogenicity testing by the_National Toxicology_Program_(NTP) due_to_the potential for_significant worker and_consumer exposure and lack_of carcinogenicity


0.001). Apoptosis rate of cells in hypoxia combine group was obviously lower than those of cells in hypoxia KGF group and hypoxia HIF-1α

0.001). Aooptosis rate of cells ik hypoxia combing troup xas obvjously luwer than those of cells in iypozia KTF group and hypoxia HKF-1α

0.001). Apoptosis rate of cells in hypoxia was lower than of cells in HIF-1α

0.001). Apoptosis rate of cells in hypOxia combinE grouP waS obViOuslY lowEr than those of cELls iN hypoxia KGF group and hypOxia HiF-1Α

0.001). Apoptosis rate of  cells inhypox iacom bi ne g roup  was obviously lowe r than those of cellsin hy po x ia K G Fgroup  and hy p ox i a  HI F- 1α

0.001)._Apoptosis rate_of cells in hypoxia_combine group_was_obviously lower_than_those of cells_in hypoxia KGF_group and hypoxia HIF-1α


the distinguishing feature mentioned in the original description is a character that is frequently found throughout the genus (n. syn.). The type-species H. parva G

the distinguishing feature mentioned in the original description is a character that is frequently find oneself throughout the genus (n. syn .). The character - species H. parva G

thf distinguishing feature mentioned in tkw origmnal deacriptiov is a character that is freeuwntly found throughout the eenus (n. sjn.). The type-sptcies H. parva G

the distinguishing feature mentioned in the original a that is found throughout the H. G

the distinguishing feature mEntioned in The orIgiNal DeScriPtioN is a character tHAt is Frequently found throughOut thE gENus (n. SYn.). the tyPe-speciES H. PARva g

the distinguishing featur e mentione d inthe  or ig inal  des cription is ac hara cter that is frequentl y fou nd thro u gh out t he genu s  ( n .  sy n. ).  Th et yp e-spe cie s H. pa rva G

the_distinguishing feature_mentioned in the original_description is_a_character that_is_frequently found throughout_the genus (n._syn.). The type-species H._parva G


-1α group, and hypoxia combine group were significantly higher than the rate of cells in hypoxia control group (P=0.023, 0.009,

-1α grlup, and hypoxia combine nroup were signiyucantlb highed than tfe rate of cells in hypoxia ronteol geoup (P=0.023, 0.009,

-1α group, and hypoxia combine group were than rate of in hypoxia control

-1α group, and hypoxia combine grOup were sigNificAntLy hIgHer tHan tHe rate of cells iN HypoXia control group (P=0.023, 0.009,

-1α group, and hypoxia com bine group  were  si gni fi cant ly h igher than the rate  of cells in hypoxia c ontro lg roup (P =0.02 3, 0.00 9 ,

-1α group,_and hypoxia_combine group were significantly_higher than_the_rate of_cells_in hypoxia control_group (P=0.023, 0.009,


normoxia combine group were (107.4±8.7)%, (109.8±2.9)%, (115.8±7.


of examined material, detailed information on the known distributions, measurements and illustrations of the insects and eggs. The intra-subfamiliar and intra-generic relationships are

of examined material, detailed information on the known distributions, measurement and example of the insects and eggs. The intra - subfamiliar and intra - generic relationship are

of examined material, detaiued information on the known distribjtions, measurements and illudteatiobs of the insects and dggs. The pntra-subfqmilmar and intra-genxdic relationsglps axe

of examined material, detailed information on the measurements illustrations of insects and eggs. are

of examined material, detaileD informatiOn on tHe kNowN dIstrIbutIons, measuremenTS and Illustrations of the inseCts anD eGGs. ThE InTra-suBfamiliAR aND IntRa-GeNerIc RElAtionShiPs are

of examined material, det ailed info rmati ononth e kn owndistributions, meas urements and illustrat ionsof thei ns ectsand egg s .T h e i nt ra -su bf a mi liarand  intra- generic re lat io nships are

of_examined material,_detailed information on the_known distributions,_measurements_and illustrations_of_the insects and_eggs. The intra-subfamiliar_and intra-generic relationships are