"Chromosomes, Mammalian" 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.
Complex nucleoprotein structures which contain the genomic DNA and are part of the CELL NUCLEUS of MAMMALS.
| Descriptor ID |
D033481
|
| MeSH Number(s) |
A11.284.187.520 G05.360.162.520
|
| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Chromosomes, Mammalian".
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Mammalian".
This graph shows the total number of publications written about "Chromosomes, Mammalian" by people in this website by year, and whether "Chromosomes, Mammalian" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 1 | 0 | 1 |
| 2003 | 2 | 0 | 2 |
| 2004 | 0 | 1 | 1 |
| 2005 | 0 | 2 | 2 |
| 2007 | 2 | 0 | 2 |
| 2008 | 0 | 1 | 1 |
| 2009 | 0 | 2 | 2 |
| 2010 | 1 | 0 | 1 |
| 2012 | 2 | 0 | 2 |
| 2013 | 1 | 3 | 4 |
| 2014 | 0 | 2 | 2 |
| 2015 | 1 | 1 | 2 |
| 2016 | 2 | 1 | 3 |
| 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Chromosomes, Mammalian" by people in Profiles.
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Loss of a 7q gene, CUX1, disrupts epigenetically driven DNA repair and drives therapy-related myeloid neoplasms. Blood. 2021 09 02; 138(9):790-805.
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Loss of Mll3 Catalytic Function Promotes Aberrant Myelopoiesis. PLoS One. 2016; 11(9):e0162515.
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Reversal of dendritic phenotypes in 16p11.2 microduplication mouse model neurons by pharmacological targeting of a network hub. Proc Natl Acad Sci U S A. 2016 07 26; 113(30):8520-5.
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Life history effects on the molecular clock of autosomes and sex chromosomes. Proc Natl Acad Sci U S A. 2016 Feb 09; 113(6):1588-93.
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A Chromosome 13 locus is associated with male-specific mortality in mice. Aging Clin Exp Res. 2016 Feb; 28(1):59-67.
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Constraints contributed by chromatin looping limit recombination targeting during Ig class switch recombination. J Immunol. 2015 Mar 01; 194(5):2380-9.
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Discovery and refinement of muscle weight QTLs in B6 × D2 advanced intercross mice. Physiol Genomics. 2014 Aug 15; 46(16):571-82.
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Annexin A6 modifies muscular dystrophy by mediating sarcolemmal repair. Proc Natl Acad Sci U S A. 2014 Apr 22; 111(16):6004-9.
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The circadian clock gene Csnk1e regulates rapid eye movement sleep amount, and nonrapid eye movement sleep architecture in mice. Sleep. 2014 Apr 01; 37(4):785-93, 793A-793C.
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A point mutation in the gene for asparagine-linked glycosylation 10B (Alg10b) causes nonsyndromic hearing impairment in mice (Mus musculus). PLoS One. 2013; 8(11):e80408.