"Alleles" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Variant forms of the same gene, occupying the same locus on homologous CHROMOSOMES, and governing the variants in production of the same gene product.
Descriptor ID |
D000483
|
MeSH Number(s) |
G05.360.340.024.340.030
|
Concept/Terms |
Alleles- Alleles
- Allele
- Allelomorphs
- Allelomorph
|
Below are MeSH descriptors whose meaning is more general than "Alleles".
Below are MeSH descriptors whose meaning is more specific than "Alleles".
This graph shows the total number of publications written about "Alleles" by people in this website by year, and whether "Alleles" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1995 | 0 | 2 | 2 |
1996 | 0 | 4 | 4 |
1997 | 0 | 8 | 8 |
1998 | 1 | 7 | 8 |
1999 | 2 | 7 | 9 |
2000 | 1 | 6 | 7 |
2001 | 0 | 6 | 6 |
2002 | 0 | 8 | 8 |
2003 | 5 | 6 | 11 |
2004 | 1 | 10 | 11 |
2005 | 1 | 12 | 13 |
2006 | 2 | 11 | 13 |
2007 | 0 | 6 | 6 |
2008 | 1 | 15 | 16 |
2009 | 2 | 13 | 15 |
2010 | 1 | 14 | 15 |
2011 | 2 | 13 | 15 |
2012 | 1 | 15 | 16 |
2013 | 2 | 22 | 24 |
2014 | 2 | 10 | 12 |
2015 | 0 | 7 | 7 |
2016 | 0 | 12 | 12 |
2017 | 1 | 4 | 5 |
2018 | 1 | 0 | 1 |
2019 | 0 | 7 | 7 |
2020 | 2 | 5 | 7 |
2021 | 0 | 7 | 7 |
2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Alleles" by people in Profiles.
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PILRA polymorphism modifies the effect of APOE4 and GM17 on Alzheimer's disease risk. Sci Rep. 2022 08 02; 12(1):13264.
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Targeted Therapy for BRAF Mutant Brain Tumors. Curr Treat Options Oncol. 2021 10 06; 22(11):105.
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Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants. Circulation. 2021 11 16; 144(20):1600-1611.
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Average semivariance yields accurate estimates of the fraction of marker-associated genetic variance and heritability in complex trait analyses. PLoS Genet. 2021 08; 17(8):e1009762.
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Defining Gene Functions in Tumorigenesis by Ex vivo Ablation of Floxed Alleles in Malignant Peripheral Nerve Sheath Tumor Cells. J Vis Exp. 2021 08 25; (174).
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Computational analysis of deleterious single nucleotide polymorphisms in catechol O-Methyltransferase conferring risk to post-traumatic stress disorder. J Psychiatr Res. 2021 06; 138:207-218.
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Genetic architectures of proximal and distal colorectal cancer are partly distinct. Gut. 2021 07; 70(7):1325-1334.
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Inhibitory Fc? Receptor and Paired Immunoglobulin Type 2 Receptor Alpha Genotypes in Alzheimer's Disease. J Alzheimers Dis. 2021; 84(3):965-968.
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Deep sequencing reveals a DAP1 regulatory haplotype that potentiates autoimmunity in systemic lupus erythematosus. Genome Biol. 2020 11 19; 21(1):281.
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An Ig ? Marker Genotype Is a Strong Risk Factor for Alzheimer Disease, Independent of Apolipoprotein E e4 Genotype. J Immunol. 2020 09 01; 205(5):1318-1322.