https://www.sciencenews.org/article/gene-variant-tied-human-aging
Gene Variant Tied to Human Aging
Aug 8, 2019 - Variants of a gene linked to mouse aging are more prevalent in elderly people than in newborns, suggesting that the gene influences human aging or specific...
gene varianttiedhumanaging
https://www.mpg.de/15451493/neandertal-genes-covid19
Neandertal gene variant increases risk of severe Covid-19 | Max-Planck-Gesellschaft
A segment of DNA that causes their carriers to have an up to three times higher risk of developing severe Covid-19 is inherited from Neandertals
gene variant
https://www.prnewswire.com/news-releases/two-faced-gene-variant-appears-good-for-men-bad-for-women-302501576.html
Two-faced gene variant appears good for men, bad for women
/PRNewswire/ -- A tiny gene variant found in skeletal muscle cells appears to have powerful-yet-opposing effects on health for men and women, according to...
good for mentwo facedgene variantappearsbad
https://www.sciencenews.org/article/blindness-hazard-gene-variant-tied-macular-degeneration
Blindness Hazard: Gene variant tied to macular degeneration
Aug 8, 2019 - People who make a particular form of an immune system protein have a heightened risk of developing old-age blindness.
gene variantblindnesshazardtiedmacular
https://www.sciencedaily.com/releases/2022/09/220921093022.htm
Rare human gene variant in ADHD, autism exposes fundamental sex differences | ScienceDaily
Key differences in male and female mice brains provide new insights into how sex determines the mechanisms by which distinct synapses monitor and regulate...
human geneadhd autism
https://www.sciencedaily.com/releases/2011/03/110309131946.htm
Gene variant influences chronic kidney disease risk | ScienceDaily
Scientists have identified a single genetic mutation in the CUBN gene that is associated with albuminuria both with and without diabetes. Albuminuria is a...
chronic kidney diseasegene variantinfluencesrisksciencedaily
https://www.sciencedaily.com/releases/2015/08/150827083426.htm
Link between gene variant and aggression in children | ScienceDaily
Researchers have found a correlation between aggression and the particular gene variants present in children when they had experienced or not experienced...
aggression in childrengene variantsciencedaily
https://www.sciencealert.com/this-rare-gene-variant-seems-to-protect-you-from-alzheimers-disease
This Rare Gene Variant Seems to Protect You From Alzheimer's Disease : ScienceAlert
Jun 24, 2024 - A woman in Colombia with rare genetic resistance to Alzheimer's disease may have more company than scientists thought.
to protect you
https://medcraveonline.com/IJFCM/variant-p190-of-the-bcr-abl1-gene-in-a-pediatric-patient-with-chronic-myeloid-leukemia.html
Variant p190 of the BCR-ABL1 gene in a pediatric patient with chronic myeloid leukemia - MedCrave...
Chronic myeloid leukemia is a clonal disease characterized by the overproduction of cells of the myeloid lineage, this entity affects mainly adults, describing...
https://www.ncbi.nlm.nih.gov/gene/2120
ETV6 ETS variant transcription factor 6 [Homo sapiens (human)] - Gene - NCBI
transcription factorhomo sapienshuman geneetv6ets
https://elifesciences.org/articles/94075
Germline cis variant determines epigenetic regulation of the anti-cancer drug metabolism gene...
A genetic variant within a newly identified enhancer regulates the expression of a key pharmacogene and alters the balance between resistance and sensitivity...
https://www.frontiersin.org/journals/pediatrics/articles/10.3389/fped.2025.1525846/full
Frontiers | Identification of a pathogenic founder variant in the WFS1 gene that causes Wolfram...
ContextWolfram syndrome (WS) is an autosomal recessive neurodegenerative disorder caused by pathogenic variants in the WFS1 gene. It is characterized by cent...
https://pmc.ncbi.nlm.nih.gov/articles/PMC44378/
The H1A histone variant is an in vivo repressor of oocyte-type 5S gene transcription in Xenopus...
Previous in vitro transcription studies have pointed to the importance of histone H1 for repression of oocyte-type 5S genes of Xenopus laevis. It has been...
https://www.questdiagnostics.com/healthcare-professionals/clinical-education-center/conference-presentations/2020/gene-specific-variant-interpretation-guidelines-in-gck--hnf1a--
Gene specific Variant Interpretation Guidelines in GCK HNF1A and HNF4A Update from the ClinGen...
Conference presentation with the title "Gene-specific Variant Interpretation Guidelines in GCK, HNF1A, and HNF4A: Update from the ClinGen Monogenic Diabetes...
https://www.sciencealert.com/scientists-find-gene-variant-giving-up-to-70-protection-against-alzheimers
Scientists Find Gene Variant Giving Up to 70% Protection Against Alzheimer's : ScienceAlert
Apr 12, 2024 - A newly discovered variant in the FN1 gene, which is responsible for making the fibronectin protein, reduces the likelihood of developing Alzheimer's by up to...
https://www.muni.cz/en/research/publications/1391540
Interleukin-17A gene variant and allergic asthma in the Czech population | Masaryk University | MUNI
https://www.sciencedaily.com/releases/2016/03/160303133001.htm
Common genetic variant in a tumor suppressor gene linked to obesity and type 2 diabetes |...
P53, a tumor suppressor referred to as has often been described as the 'guardian of the genome,' may also be the 'guardian of obesity.' New research found that...
https://www.spandidos-publications.com/10.3892/mmr.2020.11331
Identification of a novel homozygous variant in the CNGA1 gene in a Chinese family with autosomal...
Covers molecular medicine topics such as pharmacology, pathology, genetics, neuroscience, infectious diseases, molecular cardiology, and molecular surgery.
https://www.sciencedaily.com/releases/2021/12/211202162137.htm
Researchers link new gene variant in Amish population to lower risk of heart disease | ScienceDaily
Researchers have discovered a new gene variant associated with lower levels of heart-damaging LDL cholesterol and a blood clotting protein called fibrinogen...
https://www.mentalfloss.com/science/young-readers-gene-variant-are-far-more-likely-be-nearsighted
Young Readers With This Gene Variant Are Far More Likely to Be Nearsighted
Sep 10, 2015 - A new study says that kids with a specific gene variant who read at least an hour a day are five times more likely to develop myopia.
https://www.preprints.org/manuscript/202507.2240
A Novel Pathogenic Variant of the AVPR2 Gene Leading to Arginine Vasopressin Resistance from the...
Diabetes insipidus (DI) in newborn is an extremely rare condition, simultaneously the age of presentation is a strong suggestion of genetic background of...
https://www.elsevier.es/en-revista-neurologia-english-edition--495-pdf-S2173580822000876
Variant rs4149584 (R92Q) of the TNFRSF1A gene in patients with familial multiple sclerosis
https://www.wikidata.org/wiki/Q42820386
Rearrangement of immunoglobulin kappa gene in a variant-type Burkitt lymphoma cell line, KOBK101,...
scientific article published on January 1986
https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2024.1390924/full
Frontiers | Identification of a novel ANK1 gene variant c.1504-9GA and its mechanism of intron...
Objective: The objective of this study was to pinpoint pathogenic genes and assess the mutagenic pathogenicity in two pediatric patients with hereditary sphe...
https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2022.755693/full
Frontiers | Locating a novel autosomal recessive genetic variant in the cattle glucokinase gene...
New Mendelian genetic conditions arise all the time. To manage them effectively methods need to be devised that are quick and accurate. Until recently, findi...
https://www.mdpi.com/2077-0383/11/8/2223
Combination of HLA-DQ2/-DQ8 Haplotypes and a Single MSH5 Gene Variant in a Polish Population of...
Patients with type 1 diabetes (T1D) are at increased risk for developing celiac disease (CD). The aim of the study was to assess the usefulness of...
https://www.scirp.org/journal/paperinformation?paperid=74723
The Identification of a Novel, High Frequency Variant in the Cytochrome b Gene in an Isolated...
The spined loach Cobitis taenia, is listed as a protected species under Appendix 3 of the Bern Convention and Annex II of the European Council Directive...
https://www.muni.cz/en/research/publications/1536880
Novel de novo frameshift variant in the ASXL3 gene in a child with microcephaly and global...
https://www.genomenon.com/
Genomenon | Genomic Evidence at the Gene and Variant Level
the genegenomicevidencevariantlevel
https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2020.539862/full
Frontiers | A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated...
Ephb6 gene knockout causes hypertension in castrated mice. EPHB6 controls catecholamine secretion by adrenal gland chromaffin cells (AGCCs) in a testosterone...
https://www.post-gazette.com/news/science/2023/07/19/covid-genes-symptoms-study-coronavirus-hla/stories/202307190113
Gene variant may be why some test positive for virus with no COVID symptoms | Pittsburgh...
https://www.uclahealth.org/news/release/worlds-largest-dna-scan-for-autism-uncovers-new-gene-variant-for-disorder
World's largest DNA scan for autism uncovers new gene variant for disorder | UCLA Health
UCLA scientists, in partnership with 30 research institutions across the country, have identified a new gene variant that is highly common in autistic children.
https://www.ncbi.nlm.nih.gov/gene/395750
ETV6 ETS variant 6 [Gallus gallus (chicken)] - Gene - NCBI
etv6etsvariantgalluschicken
https://pmc.ncbi.nlm.nih.gov/articles/PMC12235499/
Neurological Disease Syndrome Caused by a STAG1 Gene Variant: A Case Report and Literature Review -...
The cohesin complex is a multifunctional unit that plays a crucial role in DNA repair, replication, chromosome segregation, and gene expression. Dysfunctions...
https://www.science20.com/news_articles/apoe4_gene_variant_linked_to_higher_risk_of_alzheimers_in_women-134171
ApoE4 Gene Variant Linked To Higher Risk Of Alzheimer's In Women | Science 2.0
Women who carry a copy of a gene variant called ApoE4 have substantially greater risk for Alzheimer's disease than men,according to an analysis of data on...
https://www.rcsb.org/structure/4JGE
RCSB PDB - 4JGE: Crystal structure of red fluorescent gene-engineered variant with improved folding...
Crystal structure of red fluorescent gene-engineered variant with improved folding - lanRFP_delS83 (Branchiostoma lanceolatum)
https://www.helsinki.fi/en/news/healthier-world/rare-gene-variant-discovered-contribute-lower-risk-pre-eclampsia-finnish-mothers
Rare gene variant discovered to contribute to lower risk of pre-eclampsia in Finnish mothers |...
Researchers at the University of Helsinki, in cooperation with two research groups in the United States, have discovered that some Finnish mothers carry rare...
https://www.sciencedaily.com/releases/2014/09/140923161225.htm
Best friends' drinking can negate protective effects of an alcohol dehydrogenase 1B gene variant |...
Alcohol use that begins during adolescence affects the development of alcohol use disorders during adulthood. A new study looks at the effects of interplay...
https://www.spandidos-publications.com/10.3892/br.2024.1855
Autosomal recessive type of dystrophic epidermolysis bullosa with a novel variant in the COL7A1 gene
Explores a wide range of biological and medical fields, including pharmacology, genetics, microbiology, neuroscience, and molecular cardiology.
https://www.medicaldaily.com/research-depression-may-be-caused-gene-variant-235827
Research: Depression may be caused by a gene variant
Jan 5, 2011 - There are many causes of depression and people may now add genes among these causes.
may beresearchdepressioncausedgene
https://www.mskcc.org/news/new-research-finds-genetic-variant-in-msi2-gene-may-prevent-certain-blood
New Research Finds Genetic Variant in the MSI2 Gene May Prevent Certain Blood Cancers | Memorial...
Scientists have discovered an inherited gene variant that may reduce the risk of developing certain blood cancers.