 Alleles
"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 |
|---|
| 1980 | 2 | 2 | 4 | | 1981 | 1 | 2 | 3 | | 1982 | 0 | 3 | 3 | | 1983 | 1 | 2 | 3 | | 1984 | 1 | 7 | 8 | | 1985 | 0 | 6 | 6 | | 1986 | 1 | 8 | 9 | | 1987 | 0 | 10 | 10 | | 1988 | 1 | 4 | 5 | | 1989 | 0 | 8 | 8 | | 1990 | 0 | 5 | 5 | | 1991 | 0 | 7 | 7 | | 1992 | 1 | 11 | 12 | | 1993 | 3 | 16 | 19 | | 1994 | 2 | 8 | 10 | | 1995 | 0 | 16 | 16 | | 1996 | 4 | 21 | 25 | | 1997 | 3 | 17 | 20 | | 1998 | 4 | 13 | 17 | | 1999 | 1 | 21 | 22 | | 2000 | 2 | 20 | 22 | | 2001 | 6 | 24 | 30 | | 2002 | 3 | 26 | 29 | | 2003 | 4 | 10 | 14 | | 2004 | 9 | 23 | 32 | | 2005 | 6 | 34 | 40 | | 2006 | 2 | 28 | 30 | | 2007 | 2 | 20 | 22 | | 2008 | 2 | 23 | 25 | | 2009 | 3 | 28 | 31 | | 2010 | 2 | 32 | 34 | | 2011 | 3 | 30 | 33 | | 2012 | 7 | 27 | 34 | | 2013 | 5 | 24 | 29 | | 2014 | 6 | 34 | 40 | | 2015 | 2 | 16 | 18 | | 2016 | 5 | 17 | 22 | | 2017 | 0 | 21 | 21 | | 2018 | 1 | 17 | 18 | | 2019 | 0 | 3 | 3 |
To return to the timeline, click here.
Below are the most recent publications written about "Alleles" by people in Profiles.
-
Osei-Owusu P, Charlton TM, Kim HK, Missiakas D, Schneewind O. FPR1 is the plague receptor on host immune cells. Nature. 2019 10; 574(7776):57-62.
-
Pierce BL, Tong L, Dean S, Argos M, Jasmine F, Rakibuz-Zaman M, Sarwar G, Islam MT, Shahriar H, Islam T, Rahman M, Yunus M, Lynch VJ, Oglesbee D, Graziano JH, Kibriya MG, Gamble MV, Ahsan H. A missense variant in FTCD is associated with arsenic metabolism and toxicity phenotypes in Bangladesh. PLoS Genet. 2019 03; 15(3):e1007984.
-
Ganapathi M, Padgett LR, Yamada K, Devinsky O, Willaert R, Person R, Au PB, Tagoe J, McDonald M, Karlowicz D, Wolf B, Lee J, Shen Y, Okur V, Deng L, LeDuc CA, Wang J, Hanner A, Mirmira RG, Park MH, Mastracci TL, Chung WK. Recessive Rare Variants in Deoxyhypusine Synthase, an Enzyme Involved in the Synthesis of Hypusine, Are Associated with a Neurodevelopmental Disorder. Am J Hum Genet. 2019 02 07; 104(2):287-298.
-
Glassberg EC, Gao Z, Harpak A, Lan X, Pritchard JK. Evidence for Weak Selective Constraint on Human Gene Expression. Genetics. 2019 02; 211(2):757-772.
-
Walters RK, Polimanti R, Johnson EC, McClintick JN, Adams MJ, Adkins AE, Aliev F, Bacanu SA, Batzler A, Bertelsen S, Biernacka JM, Bigdeli TB, Chen LS, Clarke TK, Chou YL, Degenhardt F, Docherty AR, Edwards AC, Fontanillas P, Foo JC, Fox L, Frank J, Giegling I, Gordon S, Hack LM, Hartmann AM, Hartz SM, Heilmann-Heimbach S, Herms S, Hodgkinson C, Hoffmann P, Jan Hottenga J, Kennedy MA, Alanne-Kinnunen M, Konte B, Lahti J, Lahti-Pulkkinen M, Lai D, Ligthart L, Loukola A, Maher BS, Mbarek H, McIntosh AM, McQueen MB, Meyers JL, Milaneschi Y, Palviainen T, Pearson JF, Peterson RE, Ripatti S, Ryu E, Saccone NL, Salvatore JE, Sanchez-Roige S, Schwandt M, Sherva R, Streit F, Strohmaier J, Thomas N, Wang JC, Webb BT, Wedow R, Wetherill L, Wills AG. Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Nat Neurosci. 2018 12; 21(12):1656-1669.
-
Krause MD, Huang RT, Wu D, Shentu TP, Harrison DL, Whalen MB, Stolze LK, Di Rienzo A, Moskowitz IP, Civelek M, Romanoski CE, Fang Y. Genetic variant at coronary artery disease and ischemic stroke locus 1p32.2 regulates endothelial responses to hemodynamics. Proc Natl Acad Sci U S A. 2018 11 27; 115(48):E11349-E11358.
-
Hope CM, Webber JL, Tokamov SA, Rebay I. Tuned polymerization of the transcription factor Yan limits off-DNA sequestration to confer context-specific repression. Elife. 2018 11 09; 7.
-
Szczaluba K, Chmielewska JJ, Sokolowska O, Rydzanicz M, Szymanska K, Feleszko W, Wlodarski P, Biernacka A, Murcia Pienkowski V, Walczak A, Bargel E, Królewczyk K, Nowacka A, Stawinski P, Nowis D, Dziembowska M, Ploski R. Neurodevelopmental phenotype caused by a de novo PTPN4 single nucleotide variant disrupting protein localization in neuronal dendritic spines. Clin Genet. 2018 12; 94(6):581-585.
-
Mika KM, Li X, DeMayo FJ, Lynch VJ. An Ancient Fecundability-Associated Polymorphism Creates a GATA2 Binding Site in a Distal Enhancer of HLA-F. Am J Hum Genet. 2018 10 04; 103(4):509-521.
-
Lager AM, Corradin OG, Cregg JM, Elitt MS, Shick HE, Clayton BLL, Allan KC, Olsen HE, Madhavan M, Tesar PJ. Rapid functional genetics of the oligodendrocyte lineage using pluripotent stem cells. Nat Commun. 2018 09 13; 9(1):3708.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|