"Chromosomes, Human" 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.
Very long DNA molecules and associated proteins, HISTONES, and non-histone chromosomal proteins (CHROMOSOMAL PROTEINS, NON-HISTONE). Normally 46 chromosomes, including two sex chromosomes are found in the nucleus of human cells. They carry the hereditary information of the individual.
Descriptor ID |
D002877
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MeSH Number(s) |
A11.284.187.520.300 G05.360.162.520.300
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human".
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human".
- Chromosomes, Human
- Chromosomes, Artificial, Human
- Chromosomes, Human, 1-3
- Chromosomes, Human, 13-15
- Chromosomes, Human, 16-18
- Chromosomes, Human, 19-20
- Chromosomes, Human, 21-22 and Y
- Chromosomes, Human, 4-5
- Chromosomes, Human, 6-12 and X
This graph shows the total number of publications written about "Chromosomes, Human" by people in this website by year, and whether "Chromosomes, Human" 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 |
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2002 | 0 | 1 | 1 |
2005 | 1 | 0 | 1 |
2007 | 0 | 2 | 2 |
2010 | 0 | 1 | 1 |
2012 | 0 | 1 | 1 |
2013 | 1 | 0 | 1 |
2014 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
2018 | 0 | 1 | 1 |
2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human" by people in Profiles.
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Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nat Genet. 2021 06; 53(6):817-829.
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Tissue-specific DNA methylation loss during ageing and carcinogenesis is linked to chromosome structure, replication timing and cell division rates. Nucleic Acids Res. 2018 08 21; 46(14):7022-7039.
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Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ? cleft palate and cleft palate only. Hum Mol Genet. 2017 02 15; 26(4):829-842.
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Nonsyndromic cleft lip with or without cleft palate in arab populations: genetic analysis of 15 risk loci in a novel case-control sample recruited in Yemen. Birth Defects Res A Clin Mol Teratol. 2014 Apr; 100(4):307-13.
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Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. Nat Genet. 2013 Oct; 45(10):1221-1225.
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Use of multilocus methylation-specific single nucleotide primer extension (MS-SNuPE) technology in diagnostic testing for human imprinted loci. Epigenetics. 2012 May; 7(5):473-81.
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Genomic and geographic distribution of SNP-defined runs of homozygosity in Europeans. Hum Mol Genet. 2010 Aug 01; 19(15):2927-35.
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Genetics of dyslexia: the evolving landscape. J Med Genet. 2007 May; 44(5):289-97.
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Self-alignments to detect mutually exclusive exon usage. In Silico Biol. 2007; 7(6):613-21.
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Methods for isolating circulating epithelial cells and criteria for their classification as carcinoma cells. Cytotherapy. 2005; 7(2):171-85.