"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
|
| MeSH Number(s) |
D12.776.660.235 D12.776.664.235
|
| 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
|
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 |
|---|
| 2008 | 2 | 0 | 2 |
| 2012 | 2 | 0 | 2 |
| 2013 | 1 | 1 | 2 |
| 2014 | 1 | 0 | 1 |
| 2015 | 2 | 0 | 2 |
| 2016 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 0 | 1 | 1 |
| 2020 | 1 | 2 | 3 |
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Below are the most recent publications written about "Chromosomal Proteins, Non-Histone" by people in Profiles.
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Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder. Genet Med. 2021 02; 23(2):384-395.
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Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans. Mutat Res Genet Toxicol Environ Mutagen. 2020 Oct - Dec; 858-860:503253.
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YBX1 Indirectly Targets Heterochromatin-Repressed Inflammatory Response-Related Apoptosis Genes through Regulating CBX5 mRNA. Int J Mol Sci. 2020 Jun 23; 21(12).
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The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome. Genet Med. 2019 06; 21(6):1295-1307.
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De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development. Nat Genet. 2017 Feb; 49(2):249-255.
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Genome-wide association study identifies multiple susceptibility loci for multiple myeloma. Nat Commun. 2016 07 01; 7:12050.
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De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment. Am J Hum Genet. 2015 Sep 03; 97(3):493-500.
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SWP73 Subunits of Arabidopsis SWI/SNF Chromatin Remodeling Complexes Play Distinct Roles in Leaf and Flower Development. Plant Cell. 2015 Jul; 27(7):1889-906.
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Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region. Birth Defects Res A Clin Mol Teratol. 2014 Jun; 100(6):512-7.
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Whole-genome paired-end analysis confirms remarkable genomic stability of atypical teratoid/rhabdoid tumors. Genes Chromosomes Cancer. 2013 Oct; 52(10):983-5.
MeSH information
