"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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| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 2 | 1 | 3 |
| 2005 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2010 | 2 | 0 | 2 |
| 2011 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Mammalian" by people in Profiles.
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Altomare DA, Menges CW, Xu J, Pei J, Zhang L, Tadevosyan A, Neumann-Domer E, Liu Z, Carbone M, Chudoba I, Klein-Szanto AJ, Testa JR. Losses of both products of the Cdkn2a/Arf locus contribute to asbestos-induced mesothelioma development and cooperate to accelerate tumorigenesis. PLoS One. 2011 Apr 19; 6(4):e18828.
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Poon A, Li Z, Wolfe GW, Lu L, Williams RW, Hayes NL, Nowakowski RS, Goldowitz D. Identification of a Chr 11 quantitative trait locus that modulates proliferation in the rostral migratory stream of the adult mouse brain. Eur J Neurosci. 2010 Aug; 32(4):523-37.
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Ferraro TN, Smith GG, Schwebel CL, Doyle GA, Ruiz SE, Oleynick JU, Lohoff FW, Berrettini WH, Buono RJ. Confirmation of multiple seizure susceptibility QTLs on chromosome 15 in C57BL/6J and DBA/2J inbred mice. Physiol Genomics. 2010 Sep; 42A(1):1-7.
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Jiao Y, Cai C, Kermany MH, Yan J, Cai Q, Miller D, Goldowitz D, Li X, Yoo TJ, Gu W. ENU induced single mutation locus on chr 16 leads to high-frequency hearing loss in mice. Genes Genet Syst. 2009 Jun; 84(3):219-24.
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Jones HC, Chen GF, Yehia BR, Carter BJ, Akins EJ, Wolpin LC. Single and multiple congenic strains for hydrocephalus in the H-Tx rat. Mamm Genome. 2005 Apr; 16(4):251-61.
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Koratkar R, Silverman KA, Pequignot E, Hauck WW, Buchberg AM, Siracusa LD. Analysis of reciprocal congenic lines reveals the C3H/HeJ genome to be highly resistant to ApcMin intestinal tumorigenesis. Genomics. 2004 Nov; 84(5):844-52.
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Cha KB, Karolyi IJ, Hunt A, Wenglikowski AM, Wilkinson JE, Dolan DF, Dootz G, Finnegan AA, Seasholtz AF, Hankenson KD, Siracusa LD, Camper SA. Skeletal dysplasia and male infertility locus on mouse chromosome 9. Genomics. 2004 Jun; 83(6):951-60.
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Ferraro TN, Golden GT, Smith GG, Martin JF, Lohoff FW, Gieringer TA, Zamboni D, Schwebel CL, Press DM, Kratzer SO, Zhao H, Berrettini WH, Buono RJ. Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene. Mamm Genome. 2004 Apr; 15(4):239-51.