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Which bacteria cause diphtheria?
Diphtheria is caused by the bacteria: 1) Corynebacterium ulcerans and 2) Corynebacterium diphtheriae.
2,028
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Which genes have been found mutated in Gray platelet syndrome patients?
The genetic defects responsible for gray platelet syndrome are mutations in the genes NBEAL2, GATA1 and GFI1B.
1,649
[ 23861251, 21765411, 21765412, 17209061, 21765413, 24325358, 23100277 ]
What is the characteristic domain of histone methyltransferases?
SET (suppressor of variegation, enhancer of zest and trithorax) domain
1,348
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What is clathrin?
Clathrin helps build small vesicles in order to safely transport molecules within and between cells.
65
[ 24307937, 19809570, 24257253, 23093191, 12952941, 24280271, 24299503, 21445329, 24322426, 24263003, 22042622 ]
For which indications has midostaurin received FDA and EMA approval?
Midostaurin was approved by the Food and Drug Administration (FDA) and the European Medical Agency (EMA) for acute myeloid leukemia with activating FLT3 mutations in combination with intensive induction and consolidation therapy as well as aggressive systemic mastocytosis (ASM), systemic mastocytosis with associated hematological neoplasm (SM-AHN) or mast cell leukemia (MCL).
2,937
[ 30069632 ]
Does an interferon (IFN) signature exist for SLE patients?
Interferon type I (IFN-I) plays a pivotal role in the pathogenesis of SLE. An IFN-I score (positive or negative), as a measure of IFN-I activation, is assessed using the expression values of IFN-I signature genes (IFI44, IFI44L, IFIT1, Ly6e, MxA, IFITM1) in CD14+ monocytes of cSLE patients and healthy controls (HCs).
3,543
[ 28830352, 21576205, 29850618, 29321042 ]
Name triad of Wernicke encephalopathy.
Wernicke's encephalopathy is a triad of ophthalmoplegia, ataxia and confusion seen in alcoholics with dietary vitamin B1 (thiamine) deficiency.
1,715
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Which is the most abundant membrane protein on Earth?
LHCII, the largest plant photosynthetic pigment-protein complex of photosystem II, is a most abundant membrane protein in living organisms and comprises approximately half of the pool of chlorophyll molecules in the biosphere.
1,390
[ 19403948, 24018323, 16307124, 23933017, 23298812, 21718685 ]
Which cancer can be treated with Darolutamide?
Darolutamide is used for treatment of nonmetastatic castration-resistant prostate cancer.
3,866
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Describe the mechanism of action of Lurbinectedin.
Lurbinectedin is a novel highly selective inhibitor of RNA polymerase II triggering caspase-dependent apoptosis of cancerous cells. It inhibits active transcription of protein-coding genes, causing DNA-break accumulation, apoptosis and modulation of the tumor microenvironment.
3,026
[ 30362375, 30153704, 30240327, 29883879, 28683469, 30090974, 27630271 ]
What is the function of cryptochrome-1 in mouse?
Cryptochrome-1 (Cry1) is an essential component of the central and peripheral circadian clocks for generation of circadian rhythms in mice.
803
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Which polyQ tract protein is linked to Spinocerebellar Ataxia type 2?
Ataxin-2 is an evolutionarily conserved protein first identified in humans as responsible for spinocerebellar ataxia type 2 (SCA2). The molecular basis of SCA2 is the expansion of a polyglutamine tract in Ataxin-2, encoding a Lsm domain that may bind RNA and a PAM2 motif that enables interaction with the poly (A) binding protein.
718
[ 19625506, 25027299, 24486837, 10973246 ]
What is a benefit of being g6PD-deficient?
Increased resistance to malaria, reduces the risk of coronary diseases, beneficial effect in terms of longevity
1,381
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Is αCGRP a member of the CGRP family?
Yes, aCGRP, a 37-residue-long peptide hormone, is a novel amyloidogenic member of the CGRP family.
3,736
[ 29501724 ]
What treatment was studied in the KEYNOTE-522 trial?
KEYNOTE-522 trial studied adjuvant pembrolizumab for patients with triple-negative breast cancer.
4,384
[ 31420357, 32870473, 32709714, 20007090, 32396855, 32101663 ]
What is SCENAR therapy used for?
all patients experienced substantial relief of pain from the first treatment. an electronic biofeedback device (scenar) may be successfully utilized in the management of post-herpetic neuralgia. scenar) as effective in the treatment of neurogenic dysfunction of the bladder in children with nocturnal enuresis. post-herpetic neuralgia using a bioelectronical device (scenar). addition of scenar therapy to the complex conventional pharmacotherapy fastened ulcer healing, increased the effectiveness of helicobacter pylori eradication, and improved the condition of the gastroduodenal mucosa. scenar therapy to patients with localized suppurative peritonitis in the postoperative period. a new technique of low-frequency modulated electric current therapy, scenar therapy, was used in treatment of 103 patients with duodenal ulcer (du).
1,127
[ 20396722, 20879466, 8779182, 16924799 ]
What disease is treated with Laparoscopic Heller Myotomy (LHM)?
To compare the outcome of per oral endoscopic myotomy (POEM) and laparoscopic Heller myotomy (LHM) for the treatment of esophageal achalasia
2,895
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What is the cause of Phthiriasis Palpebrarum?
Phthiriasis palpebrarum is a rare eyelid infestation caused by phthirus pubis.
894
[ 20339456, 12898406, 12523816, 22707338, 26451147, 24909484, 24157356, 16903509, 19728949, 24556565, 23993722 ]
What is the role of PCAT6 in human cancers?
PCAT6, is a carcinogenic lncRNA. It is abnormally elevated in various human malignant tumors. PCAT6 has been found to sponge various miRNAs to activate the signaling pathways, which further affects tumor cell proliferation, migration, invasion, cycle, apoptosis, radioresistance, and chemoresistance. It is believed to have diagnostic and prognostic value and clinical applications in various human malignancies.
4,707
[ 34885209, 31676070 ]
Does tremelimumab improve survival of mesothelioma patients?
No. Tremelimumab did not significantly prolong overall survival compared with placebo in patients with previously treated malignant mesothelioma.
2,876
[ 28729154, 29773326, 28231719 ]
Is Sotatercept effective for Pulmonary Arterial Hypertension?
Sotatercept was shown to be effective for Pulmonary Arterial Hypertension.
4,419
[ 33789009, 33733610 ]
Are the members of the KRAB-ZNF gene family promoting gene repression?
The stem cell zinc finger 1 (SZF1)/ZNF589 protein belongs to the large family of Kruppel-associated box domain-zinc finger (KRAB-ZNF) transcription factors, which are present only in higher vertebrates and epigenetically repress transcription by recruiting chromatin-modifying complexes to the promoter regions of their respective target genes Because KAP1 is recruited to the DNA via interaction with KRAB-ZNF proteins, we suggest that expression of KRAB-ZNF genes may be controlled via an auto-regulatory mechanism involving KAP1.
3,471
[ 29198826, 26814189, 30444046, 26738774, 17542650 ]
What is the aim of the 4D nucleome project?
The 4D Nucleome Network aims to develop and apply approaches to map the structure and dynamics of the human and mouse genomes in space and time with the goal of gaining deeper mechanistic insights into how the nucleus is organized and functions. The project will develop and benchmark experimental and computational approaches for measuring genome conformation and nuclear organization, and investigate how these contribute to gene regulation and other genome functions.
2,539
[ 28905911 ]
Was vivotif licensed in Europe and the US at the same time?
No, vivotif was licensed in Europe in 1983 and in the US in 1989.
3,711
[ 28515625 ]
Does GC content vary markedly within a given isochore?
Isochores are relatively long regions with a relatively homogeneous GC content, and with rather sharp boundaries with neighboring isochores. The base composition, and thus the GC content may differ between different isochores, but is more or less consistent within a given isochore.
766
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What is the link between HOT regions and RNA polymerase recruitment?
Most HOT regions co-localize with RNA polymerase II binding sites, but many are not near the promoters of annotated genes. At HOT promoters, TF occupancy is strongly predictive of transcription preinitiation complex recruitment and moderately predictive of initiating Pol II recruitment, but only weakly predictive of elongating Pol II and RNA transcript abundance.
586
[ 24138567 ]
Which is the target protein of the drug nivolumab?
Nivolumab was developed as a monoclonal antibody against programmed death receptor-1, an immune checkpoint inhibitor which negatively regulates T-cell proliferation and activation.
590
[ 26406148, 25897158, 26027431, 26273207, 26448890, 26028407 ]
List diseases caused by protein glutamine expanded repeats
Huntington's Disease, dentatorubral-pallidoluysian atrophy
2,717
[ 22905336, 10434299, 9735324, 10381356 ]
Can Diabetes be caused by a defect in a potassium chanel?
Mutations in the KATP channel can lead to neonatal diabetes.
1,846
[ 27118464, 25931474, 24827651, 15746700 ]
How does adrenergic signaling affect thyroid hormone receptors?
alpha1- adrenergic signalling increases TRalpha1 expression in nucleus and decreases TRalpha1 expression in cytosol.
1,232
[ 18622044 ]
From which sequence does the Alu repeat originate from?
The presence of Alu-like structural motifs supports the hypothesis of the monophyletic origin of Alu and B1 repeats, i.e., from a common 7SL RNA-derived retroposing monomeric element, The origin of Alu subfamilies in human populations may be related to evolution of chromosome Y.
1,093
[ 16343813, 8576966, 12815945, 9694666, 12167372, 9395063 ]
Is siltuximab effective for Castleman disease?
Yes, siltuximab , a chimeric human-mouse monoclonal antibody to IL6, is approved for the treatment of patients with multicentric Castleman disease who are human immunodeficiency virus negative and human herpesvirus-8 negative.
2,021
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What is known about the value of mindfulness interventions in prostate cancer patients?
In prostate cancer patients, mindfulness interventions were well accepted and were effective in reducing stress, anxiety, avoidance, fear of cancer recurrence, cortisol levels and blood pressure, and improving quality of life, sleep quality and immune system functioning. In addition, mindfulness interventions promoted initiation of healthy dietary changes and decreases the rate of PSA increase and may slow the rate of tumor progression in cases of biochemically recurrent prostate cancer.
394
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What does the strimvelis treatment consist of?
Strimvelis consists of autologous CD34+ cells transduced to express adenosine deaminase [ADA].
3,197
[ 29625577 ]
List bacteria that may be useful in uranium bioremediation.
The main bacteria studied in uranium bioremediation are Geobacteraceae. Other bacteria are: Firmicutes, Shewanella oneidensis Pseudomonas aeruginosa Anaeromyxobacter dehalogenans strain Rf4T
1,314
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How does botulism toxin act on the muscle?
. The seven immunologically distinct serotypes of BoNTs (A-G), each produced by various strains of Clostridium botulinum, act on the neuromuscular junction by blocking the release of the neurotransmitter acetylcholine, thereby resulting in flaccid muscle paralysis.
2,980
[ 14747968, 28569348, 1311751, 20178376, 9339823 ]
What is hyperosmia
Hyperosmia is increased olfactory acuity
131
[ 24302690, 23520356, 21250223 ]
What is the the Menzerath-Altmann law?
Recently, a random breakage model has been proposed to explain the negative correlation between mean chromosome length and chromosome number that is found in many groups of species and is consistent with Menzerath-Altmann law, a statistical law that defines the dependency between the mean size of the whole and the number of parts in quantitative linguistics. The random breakage and variants keeping genome size and chromosome number independent raise no serious objection to the relevance of correlations consistent with Menzerath-Altmann law across taxonomic groups and the possibility of a connection between human language and genomes through that law.
1,481
[ 22197514 ]
What is Morton's Neuroma?
Morton's neuroma (MN) is a neuralgia involving the common plantar digital nerves of the metatarsal region.
4,406
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What is PARP inhibitor (PARPi) resistance?
PARPi has been designed and tested for many years and became a potential supplement for the conventional chemotherapy. However, increasing evidence indicates the appearance of the resistance to this treatment. Specifically, cancer cells may acquire new mutations or events that overcome the positive effect of these drugs.
2,596
[ 28255272, 28510338, 28069876 ]
What is the mechanism of the drug CRT0066101?
Recently developed small molecule PKD inhibitors, CID755673 and CRT0066101, provide potentially important pharmacological approaches to further investigate the effect of PKD in pancreatitis therapy
3,064
[ 26797128, 26895471, 20947701, 29270134, 29071385, 27030010, 25852060, 20442301 ]
What is the phenotype of people carrying mutations in the gene PRDM12?
New therapeutic options have recently been derived from studies of individuals with congenital insensitivity to pain (CIP). Here we identified 10 different homozygous mutations in PRDM12 (encoding PRDI-BF1 and RIZ homology domain-containing protein 12) in subjects with CIP from 11 families.
2,189
[ 26005867, 26549885, 25891934 ]
Which syndrome is caused by deletion of Pds5b in mice?
Mice lacking sister chromatid cohesion protein Pds5b exhibit developmental abnormalities reminiscent of Cornelia de Lange syndrome.
2,094
[ 19412548, 17652350 ]
Name a CFL2 mutation which is associated with nemaline myopathy?
A mutation in CFL2 was identified in a family with nemaline myopathy, namely a homozygous missense mutation in exon 2 (c.19G>A, p.Val7Met).
3,179
[ 22560515 ]
What are the 3 types of ultraviolet (UV) solar radiation?
Solar ultraviolet (UV) radiation, an ubiquitous environmental carcinogen, is classified depending on the wavelength, into three regions; short-wave UVC (200-280 nm), mid-wave UVB (280-320 nm), and long-wave UVA (320- 400 nm)
2,732
[ 24891049, 11100018, 23834148, 16117741 ]
What does the human IVIG treatment for Alzheimer's disease contain?
Human intravenous immunoglobulin (IVIG) is a mixture of polyclonal IgG antibodies isolated and pooled from thousands of healthy human donors.
2,371
[ 25115546 ]
What is the function of WAPL protein on cohesin?
Human Wapl is a cohesin-binding protein that promotes sister-chromatid resolution in mitotic prophase We show that the human ortholog of Wapl is a cohesin-binding protein that facilitates cohesin's timely release from chromosome arms during prophase.
3,719
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What is the trade name of sildenafil?
The trade name of sildenafil is Viagra.
3,454
[ 25984278 ]
What is Tn-seq?
The transposon mutagenesis and high-throughput sequencing (Tn-seq) is a technique that allows for quantitative assessment of individual mutants within a transposon mutant library by sequencing the transposon-genome junctions and then compiling mutant presence by mapping to a base genome. Using Tn-seq, it is possible to quickly define all the insertional mutants in a library and thus identify nonessential genes under the conditions in which the library was produced. Identification of fitness of individual mutants under specific conditions can be performed by exposing the library to selective pressures.
834
[ 21053251, 25636611, 24077707, 19767758, 21253457, 23990803, 22925268, 25139902 ]
Salivary Cortisol is a biomarker for what disease/syndrome/condition?
Salivary cortisone , as a biomarker for psychosocial stress , is associated with state anxiety and heart rate . ortisol as a stress biomarker
3,203
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List symptoms of Hakim Triad.
Triad of Hakim--Adams is well known for normal pressure hydrocephalus (NPH): dementia, gait disturbances and urinary incontinence.
729
[ 21698923, 19823916, 6583309, 20568668, 21194654 ]
When is lorlatinib used?
Lorlatinib is a third-generation ALK inhibitor that can overcome the largest number of acquired ALK resistance mutations, including the solvent-front mutation G1202R.
4,495
[ 34589977, 34585621, 34548910 ]
What is the genetic basis of the Delayed Sleep-Phase Syndrome (DSPS)?
Circadian gene mutations are also associated with circadian rhythm disorders such as familial advanced sleep phase syndrome, delayed sleep phase syndrome, and non-24-hour sleep-wake syndrome. Possible association of human leucocyte antigen DR1 with delayed sleep phase syndrome. The study investigated the human leucocyte antigen (HLA), types A, B and DR, of 42 patients with delayed sleep phase syndrome (DSPS) and compared the frequencies of the antigens with those in 117 healthy controls. The comparison revealed that the gene frequencies and positivities of HLA-A, -B and -DR, except for DR1, had no significant differences between the patients and controls. The frequency of HLA-DR1 was increased in the DSPS patients as compared with that in the healthy controls (P = 0.0069 in positivity). In human leukocyte antigen (HLA) typing, the incidence of DR1 positivity alone was significantly higher in DSPS patients than in healthy subjects.
2,333
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List inflammatory caspase proteins?
caspase-1 caspase-4 caspase-5
534
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Does vesatolimod inhibit TLR7?
No, vesatolimod is an agonist of toll-like receptor 7.
2,796
[ 29104121 ]
Which drugs were tested in the CheckMate 227 clinical trial?
CheckMate-227 clinical trial tested ipilimumab plus nivolumab for the treatment of non-small cell lung cancer.
3,525
[ 29658845, 30393621, 27610613, 31066582, 31195357, 29661758 ]
Can multiple myeloma patients develop hyperviscosity syndrome?
Yes, multiple myeloma patients can develop hyperviscosity syndrome. Multiple myeloma is a neoplastic plasma-cell disorder resulting from malignant plasma cells in the bone marrow. It can cause a hyperviscosity syndrome secondary to the paraproteinaemia associated with the disease. The increased hyperviscosity can lead to retinal vein occlusions and other ocular problems.
2,451
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Is CTCF bound at nucleosome free regions?
yes, robust inter-nucleosomal interactions exist around transcription start site (TSS), transcription termination sites (TTS) or around CTCF binding sites
3,362
[ 25348714, 30414923, 30188887, 21249180, 16877759 ]
Is p100 the precursor protein molecule of the NF-kappaB transcription factor subunit p50?
No, the precursor molecule for NF-kappaB p50 is p105 and not p100. Nfkb2 encodes two members of the NF-kappa B/Rel family of proteins: p52 and p100. The p100 polypeptide has been proposed to serve as a precursor of p52 (and not of p50), which corresponds to the N-terminal half of p100. NF-kappaB functions as a hetero- or homo-dimer which can be formed from five NF-kappaB subunits, NF-kappaB1 (p50 and its precursor p105), NF-kappaB2 (p52 and its precursor p100), RelA (p65), RelB and c-Rel.
1,329
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How many groups of viruses exist in the Baltimore Classification?
There are seven "Baltimore classes" (BCs) that define the major features of virus reproduction.
3,974
[ 32132243, 28588308 ]
List mutations that are implicated in the Gray Platelet Syndrome.
GFI1B and NBEAL2 mutations are implicated in the Gray Platelet Syndrome.
998
[ 23861251, 21765412, 25258341, 21765413, 24325358, 23100277 ]
What are TAMs in cancer therapy?
TAMs are Tumor Associated Macrophages and are important in Cancer therapy.
4,267
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What is vesiduction?
'Vesiduction' as a fourth mode of intercellular DNA transfer.
4,306
[ 32784449, 32363801 ]
What is the aim of the METABRIC project?
The METABRIC [Molecular Taxonomy of Breast Cancer International Consortium] cohort aims at the integration of genomic and transcriptomic profiles of 2000 breast tumours.
2,891
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Does SARM1 deletion cause neurodegeneration?
Mouse strain with Sarm1 deletion (Sarm1-/-) is highly resistant to axon neurodegeneration.
2,619
[ 26820848 ]
Which is the definition of pyknons in DNA?
Pyknons are non-random sequence patterns significantly repeated throughout non-coding genomic DNA, which have additional nonoverlapping instances in the untranslated and protein-coding regions. They are found more frequently in the 3' untranslated regions of genes than in other regions of the human genome.
408
[ 16636294, 19833446, 19229130, 19452047, 16751093, 19052667 ]
What is PRL3-zumab?
PRL3-zumab is a first-in-class humanized antibody (PRL3-zumab) against PRL-3, an intracellular tumor-associated phosphatase upregulated in multiple human cancers, for unconventional cancer immunotherapies. PRL3-zumab specifically blocked PRL-3+, but not PRL-3-, orthotopic gastric tumors. In this setting, PRL3-zumab had better therapeutic efficacy as a monotherapy, rather than simultaneous combination with 5-fluorouracil or 5-fluorouracil alone. PRL3-zumab could also prevent PRL-3+ tumor recurrence. Mechanistically, we found that intracellular PRL-3 antigens could be externalized to become "extracellular oncotargets" that serve as bait for PRL3-zumab binding to potentially bridge and recruit immunocytes into tumor microenvironments for killing effects on cancer cells.
3,578
[ 27699276 ]
Which two drugs are included in the Entresto pill?
Entresto includes Sacubitril and Valsartan.
2,932
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Which are the consequences of the hyperphosphorylated tau in Alzheimers' Disease?
The consequences of the hyperphosphorylated tau in Alzheimers' Disease is: 1) The formation of neurofibrillary tangles (NFTs) 2) Impaired glutamate metabolism 3) Decreased tau affinity for microtubules binding 4) Dendritic and axonal instability 5) Synaptic degeneration 6) Neuronal loss.
1,787
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Which is the major function of sororin?
Sororin is a positive regulator of sister chromatid cohesion that interacts with the cohesin complex.
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Which gene is required for the efficient function of clopidogrel?
The prodrug clopidogrel requires activation by cytochrome P-450 (CYP) enzymes for its antiplatelet effect. Variability in clopidogrel response might be influenced by polymorphisms in genes coding for drug metabolism enzymes (cytochrome P450 CYP2C19), transport proteins (P-glycoprotein) and/or target proteins for the drug (adenosine diphosphate-receptor P2Y12). The CYP2C19 loss-of-function alleles had a gene dose effect on the pharmacodynamics and composite ischemic events of clopidogrel in our study population. Neither the ABCB1 nor the PON1 genotype significantly influenced the antiplatelet effect and clinical outcomes of clopidogrel in these patients
83
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When was empagliflozin FDA approved?
Empagliflozin was approved in 2014 by the European Commission and the United States Food and Drug Administration for the treatment of type 2 diabetes mellitus (T2DM).
330
[ 25712444 ]
Abnormalities in which chromosomes were linked to the Moyamoya disease?
chromosomes 3, 6, 8, 12, 15, 17, 21, X and Y were implicated in the Moyamoya disease.
198
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Is it possible to analyze exosomes with FACS?
Yes, a novel strategy for generating metabolically-labeled fluorescent exosomes that can be counted by flow cytometry assay (FACS) and characterized.
3,169
[ 30290833, 26598503, 29783743, 26154623 ]
What is the mechanism of action of geldanamycin?
Geldanamycin is an ansamycin antibiotic which holds the ability to bind heat-shock protein 90. This interaction can lead to the disruption of heat-shock protein 90-containing multimolecular complexes. Additionally, it can induce inhibition or even degradation of partner proteins dissociated from the 90 kDa chaperone and, eventually, cause apoptosis in a variety of cell types.
1,730
[ 21525416, 20534344, 18001136, 9817749, 23986774, 15971989, 23701727 ]
Have apolipoprotein mimetics been used in clinical trials?
Yes, apolipoprotein mimetics have entered clinical trials.
3,189
[ 25157031 ]
What is the role of the Ada O6-alkylguanine alkyltransferase in bacteria?
The Ada O6-methylguanine-DNA methyltransferase is a multifunctional protein, product of the ada gene. Ada functions in DNA repair by direct dealkylation of alkylated DNA lesions, such as the toxic, mutagenic and carcinogenic O6-alkylguanine (O6-AlkG) and O4-alkylthymine (O4-AlkT) which are restored to guanine and thymine. Ada accepts stoichiometrically the alkyl group from O6-alkylguanine in DNA at the Cys-321 residue and from alkyl phosphotriester at the Cys-69 residue. When methylated at Cys-69, Ada becomes a transcriptional activator of the genes in the ada regulon, including its own. The ada gene controls the inducible resistance to alkylation mutagenesis and killing (the adaptive response). Ada alkyltransferase (ATase) is induced by exposure to low doses of methylating agents. During exponential growth, Ada removes lesions responsible for G:C to A:T transitions and G:C to C:G transversions, while in stationary populations it removes lesions causing G:C to A:T and A:T to G:C transitions, and G:C to C:G, A:T to C:G, and A:T to T:A transversions. Thus, Ada protein acts both as a positive regulator of the ada response and as a DNA repair enzyme.
1,494
[ 10101186, 9366274, 7662116, 8512805, 7695814, 8195077, 9079656, 8152424, 1520330, 3526284, 3887409, 9484244, 8519412, 9717173, 7634390, 2105461, 1747932 ]
Describe the application of whole genome sequencing in the diagnosis of primary ciliary dyskinesia (PCD)
Genetic testing is an important component of diagnosing PCD, especially in cases of atypical disease history. WGS is effective in cases where prior gene panel testing has found no variants or only heterozygous variants. In these cases it may detect SVs and is a powerful tool for novel gene discovery.
4,323
[ 34556108 ]
What is known about growth arrest-specific 6 protein?
Growth arrest-specific 6 (Gas6) is a vitamin K-dependent protein secreted by immune cells, endothelial cells, vascular smooth muscle cells, and adipocytes. Recent studies indicate that Gas6 and receptors of the TAM (Tyro3, Axl, and Mer) family may be involved in the pathogenesis of obesity, systemic inflammation, and insulin resistance.
4,172
[ 30346880, 32969596, 31583710 ]
Where are integrins localized in a cell?
Integrins are transmembrane glycoproteins that are broadly distributed in living organisms.
3,890
[ 32584192, 32950537 ]
Which type of pluripotency is Otx2 associated with?
transcription factor Otx2 acts as a negative switch in the regulation of transition from naive to primed pluripotency. Otx2 and Oct4 drive early activation during embryonic stem cell transition from naive pluripotency.
3,809
[ 24338594, 27924227, 27292645, 32367046, 30567463, 29056334, 23154415, 24905168, 27019633, 23719282, 27732856, 27920151, 21062744, 27392793, 30413530, 23954875, 24931607, 30349051 ]
What is the tradename of apixaban?
The tradename of apixaban is Eliquis.
3,088
[ 23677804 ]
Are genes symmetrically distributed between leading and lagging DNA strand in bacteria?
In most bacteria, genes are preferentially encoded on the leading strand than on the lagging strand. This avoids the potentially detrimental head-on collisions that occur between the replication and transcription machineries when genes are encoded on the lagging strand. Head-on collisions are more deleterious than codirectional collisions, and may lead to replication fork arrest and genomic instability. Genes of some functional categories such as ribosome have higher preferences to be on the leading strands, while genes of other functional categories such as transcription factor have higher preferences on the lagging strands. Strand-biased gene distribution correlates with replication-associated purine asymmetry and the presence or absence of polC. Especially essential and highly transcribed genes and genes whose expression is important for fitness are more preferentially situated at the leading strand in bacteria.
1,414
[ 24273314, 19221094, 12217498, 20600808, 14743977, 15942025, 25425232, 23538833, 11677621, 20417622, 17532183, 21350489, 15823418, 22735706 ]
Nemolizumab has been shown to be effective for which disease?
Nemolizumab has been shown to be effective for atopic dermatitis.
4,369
[ 32640132, 33735876, 33644104, 29753033, 33711179, 34213742, 33924978, 32074418, 34726262, 33045848, 32507066, 31449914, 28249150, 28703903 ]
Are conserved noncoding elements associated with the evolution of animal body plans?
Yes. Cis-regulatory inputs identified by CNEs arose during the "re-wiring" of regulatory interactions that occurred during early animal evolution. Consequently, different animal groups, with different core GRNs, contain alternative sets of CNEs. Due to the subsequent stability of animal body plans, these core regulatory sequences have been evolving in parallel under strong purifying selection in different animal groups.
1,343
[ 19492354 ]
Which treatment leads to an increase in neutrophil counts in severe congenital neutropenia?
In phase I/II/III studies in patients with severe congenital and cyclic neutropenia, treatment with recombinant human granulocyte colony-stimulating factor (r-metHuG-CSF) resulted in a rise in the absolute neutrophil counts (ANC) and a reduction in infections
460
[ 7529539, 1705835, 2683920, 10779444, 21052952, 1689595, 16822461 ]
What gene is mutated in Huntington's Disease patients?
Huntington's disease (HD) is a fully penetrant neurodegenerative disease caused by a dominantly inherited CAG trinucleotide repeat expansion in the huntingtin gene HTT encoding the Huntingtin protein on chromosome 4.
3,446
[ 29172480, 12046502, 27221146, 30850940, 24296361, 23223017, 11723754, 8774958, 29178352, 25416977, 17503740, 28986324, 28817209, 9392570, 26369532 ]
What do mepolizumab and reslizumab have in common?
Mepolizumab and reslizumab are monoclonal antibodies that target and neutralize interleukin 5. They have been shown to reduce eosinophil counts and they are used for the treatment of refractory asthma (associated with eosiniphilia) and other eosinophilic diseases.
644
[ 21824072, 19037962, 22092535, 25671117, 20565230, 26285457, 22541618, 24275927, 23742015 ]
Describe what is the usage of the Theatre software tool for genomic analysis.
Theatre is a web-based computing system designed for the comparative analysis of genomic sequences, especially with respect to motifs likely to be involved in the regulation of gene expression. Theatre is an interface to commonly used sequence analysis tools and biological sequence databases to determine or predict the positions of coding regions, repetitive sequences and transcription factor binding sites in families of DNA sequences. The information is displayed in a manner that can be easily understood and can reveal patterns that might not otherwise have been noticed. In addition to web-based output, Theatre can produce publication quality colour hardcopies showing predicted features in aligned genomic sequences.
973
[ 12824356 ]
List 3 symptoms of Wernicke encephalopathy.
Wernicke's encephalopathy (WE) is a neurological syndrome caused by thiamine deficiency, and clinically characterized by ophthalmoplegia, ataxia and acute confusion.
2,554
[ 27300674, 27988455, 17698536, 25856744, 26869612, 25550705, 28289649, 22869492, 23935638, 16219837, 14644703 ]
What is the name for anorexia in gymnasts?
Anorexia athletica
1,036
[ 10551340, 24240086 ]
Are cyclophilins ubiquitously expressed?
Yes, cyps (cyclophilins) are ubiquitous proteins of the immunophilin superfamily.
1,563
[ 16928193, 19923714, 15869639, 21087465, 14568539, 25259854, 15735342, 15935056, 19403925, 17103061, 23849880, 23123451, 24887548 ]
Is istiratumab effective for pancreatic cancer?
No. In clinical trial, istiratumab failed to improve efficacy of standard of care for pancreatic cancer.
4,300
[ 31912800 ]
What is the normal function p53?
Wild-type p53 can suppress tumour development by multiple pathways.
2,921
[ 28984872, 29242642, 28749203, 28937686 ]
What is the function of CR elements in B-cells?
After addition of culture supernatant from BCG-activated macrophages CR- B cells cooperate with both unprimed and primed T helper cells.
3,725
[ 23030360, 23555858, 305444, 1083874 ]
What are the symptoms of an incidental durotomy (ID).
Incidental durotomy can cause postural headaches, nausea, vomiting, dizziness, photophobia, tinnitus, and vertigo. Meningitis is a rare complication reported to occur with a frequency of 0.18%
4,632
[ 10528385, 15260094 ]
Does amiodarone affect thyroid hormone receptors in the myocardium?
Yes
1,092
[ 9781936, 17535870, 7598731, 10445678 ]
Which gene mutations cause the Marfan syndrome?
Marfan syndrome (MFS) is an autosomal dominant disorder caused by mutations in the fibrillin 1 gene (FBN1).
2,107
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Is endostatin a proangiogenic factor?
No, endostatin is an antiangiogenic factor
404
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What are the birth defects associated with Zika-virus infection?
Although the full spectrum of adverse reproductive outcomes caused by Zika virus infection is not yet determined, a distinctive phenotype-the congenital Zika syndrome-has emerged. Zika virus infection during pregnancy is a cause of microcephaly and other severe birth defects.
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