Chromosomal Proteins, Non-Histone
"Chromosomal Proteins, Non-Histone" 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.
Nucleoproteins, which in contrast to HISTONES, are acid insoluble. They are involved in chromosomal functions; e.g. they bind selectively to DNA, stimulate transcription resulting in tissue-specific RNA synthesis and undergo specific changes in response to various hormones or phytomitogens.
Descriptor ID |
D002868
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MeSH Number(s) |
D12.776.660.235 D12.776.664.235
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Concept/Terms |
Chromosomal Proteins, Non-Histone- Chromosomal Proteins, Non-Histone
- Proteins, Non-Histone Chromosomal
- Chromosomal Proteins, Nonhistone
- Nonhistone Chromosomal Proteins
- Chromosomal Proteins, Non Histone
- Non-Histone Chromosomal Proteins
- Non Histone Chromosomal Proteins
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Below are MeSH descriptors whose meaning is more general than "Chromosomal Proteins, Non-Histone".
Below are MeSH descriptors whose meaning is more specific than "Chromosomal Proteins, Non-Histone".
This graph shows the total number of publications written about "Chromosomal Proteins, Non-Histone" by people in this website by year, and whether "Chromosomal Proteins, Non-Histone" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2013 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomal Proteins, Non-Histone" by people in Profiles.
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Ng JM, Martinez D, Marsh ED, Zhang Z, Rappaport E, Santi M, Curran T. Generation of a mouse model of atypical teratoid/rhabdoid tumor of the central nervous system through combined deletion of Snf5 and p53. Cancer Res. 2015 Nov 01; 75(21):4629-39.
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Fridley BL, Abo R, Tan XL, Jenkins GD, Batzler A, Moyer AM, Biernacka JM, Wang L. Integrative gene set analysis: application to platinum pharmacogenomics. OMICS. 2014 Jan; 18(1):34-41.
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Ward IM, Minn K, van Deursen J, Chen J. p53 Binding protein 53BP1 is required for DNA damage responses and tumor suppression in mice. Mol Cell Biol. 2003 Apr; 23(7):2556-63.
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