"Chromosomes, Human, X" 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.
The human female sex chromosome, being the differential sex chromosome carried by half the male gametes and all female gametes in humans.
Descriptor ID |
D041321
|
MeSH Number(s) |
A11.284.187.520.300.325.680 A11.284.187.865.982.500 G05.360.162.520.300.325.680 G05.360.162.865.982.500
|
Concept/Terms |
Chromosomes, Human, X- Chromosomes, Human, X
- X Chromosome, Human
- Chromosome, Human X
- Chromosomes, Human X
- Human X Chromosome
- Human X Chromosomes
- X Chromosomes, Human
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, X".
- Anatomy [A]
- Cells [A11]
- Cellular Structures [A11.284]
- Chromosomes [A11.284.187]
- Chromosomes, Mammalian [A11.284.187.520]
- Chromosomes, Human [A11.284.187.520.300]
- Chromosomes, Human, 6-12 and X [A11.284.187.520.300.325]
- Chromosomes, Human, X [A11.284.187.520.300.325.680]
- Sex Chromosomes [A11.284.187.865]
- X Chromosome [A11.284.187.865.982]
- Chromosomes, Human, X [A11.284.187.865.982.500]
- Biological Sciences [G]
- Genetic Phenomena [G05]
- Genetic Structures [G05.360]
- Chromosomes [G05.360.162]
- Chromosomes, Mammalian [G05.360.162.520]
- Chromosomes, Human [G05.360.162.520.300]
- Chromosomes, Human, 6-12 and X [G05.360.162.520.300.325]
- Chromosomes, Human, X [G05.360.162.520.300.325.680]
- Sex Chromosomes [G05.360.162.865]
- X Chromosome [G05.360.162.865.982]
- Chromosomes, Human, X [G05.360.162.865.982.500]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, X".
This graph shows the total number of publications written about "Chromosomes, Human, X" by people in this website by year, and whether "Chromosomes, Human, X" 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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2003 | 0 | 1 | 1 |
2005 | 0 | 2 | 2 |
2008 | 1 | 0 | 1 |
2009 | 1 | 2 | 3 |
2011 | 1 | 0 | 1 |
2012 | 1 | 0 | 1 |
2016 | 2 | 1 | 3 |
2019 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Chromosomes, Human, X" by people in Profiles.
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Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2. Cold Spring Harb Mol Case Stud. 2019 02; 5(1).
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Genetic mapping of 15 human X chromosomal forensic short tandem repeat (STR) loci by means of multi-core parallelization. Forensic Sci Int Genet. 2016 11; 25:39-44.
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Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder. Hum Mol Genet. 2016 08 01; 25(15):3383-3394.
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Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie Syndrome. PLoS One. 2016; 11(4):e0153757.
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Collaborative genetic mapping of 12 forensic short tandem repeat (STR) loci on the human X chromosome. Forensic Sci Int Genet. 2012 Dec; 6(6):778-84.
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Nonsense mutations in SMPX, encoding a protein responsive to physical force, result in X-chromosomal hearing loss. Am J Hum Genet. 2011 May 13; 88(5):621-7.
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X chromosomal variation is associated with slow progression to AIDS in HIV-1-infected women. Am J Hum Genet. 2009 Aug; 85(2):228-39.
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IFAP syndrome is caused by deficiency in MBTPS2, an intramembrane zinc metalloprotease essential for cholesterol homeostasis and ER stress response. Am J Hum Genet. 2009 Apr; 84(4):459-67.
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Goltz-Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap. Eur J Hum Genet. 2009 Oct; 17(10):1207-15.
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Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1. J Clin Invest. 2008 Sep; 118(9):3132-42.