"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 |
|---|
| 2002 | 2 | 1 | 3 |
| 2003 | 8 | 0 | 8 |
| 2004 | 3 | 2 | 5 |
| 2005 | 6 | 2 | 8 |
| 2006 | 2 | 6 | 8 |
| 2007 | 3 | 5 | 8 |
| 2008 | 4 | 1 | 5 |
| 2009 | 4 | 3 | 7 |
| 2010 | 7 | 5 | 12 |
| 2011 | 6 | 4 | 10 |
| 2012 | 2 | 3 | 5 |
| 2013 | 0 | 2 | 2 |
| 2014 | 4 | 1 | 5 |
| 2015 | 2 | 3 | 5 |
| 2016 | 4 | 2 | 6 |
| 2017 | 1 | 2 | 3 |
| 2018 | 2 | 1 | 3 |
| 2019 | 3 | 1 | 4 |
| 2020 | 1 | 0 | 1 |
| 2021 | 2 | 1 | 3 |
| 2023 | 0 | 1 | 1 |
| 2024 | 0 | 3 | 3 |
To return to the timeline,
click here.
Below are the most recent publications written about "Chromosomes, Human, X" by people in Profiles.
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Chromatin conformation capture in the clinic: 4C-seq/HiC distinguishes pathogenic from neutral duplications at the GPR101 locus. Genome Med. 2024 Sep 13; 16(1):112.
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X-linked genetic associations in sporadic thoracic aortic dissection. Am J Med Genet A. 2024 09; 194(9):e63644.
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ASPSCR1-TFE3 reprograms transcription by organizing enhancer loops around hexameric VCP/p97. Nat Commun. 2024 Feb 07; 15(1):1165.
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Parental age effects and Rett syndrome. Am J Med Genet A. 2024 02; 194(2):160-173.
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Molecular and clinical insights into complex genomic rearrangements related to MECP2 duplication syndrome. Eur J Med Genet. 2021 Dec; 64(12):104367.
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Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices. Nat Commun. 2021 04 12; 12(1):2182.
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SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females. Am J Hum Genet. 2021 03 04; 108(3):502-516.
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Abnormal X chromosome inactivation and tumor development. Cell Mol Life Sci. 2020 Aug; 77(15):2949-2958.
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Identification of cancer sex-disparity in the functional integrity of p53 and its X chromosome network. Nat Commun. 2019 11 26; 10(1):5385.
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X-chromosome association studies of congenital heart defects. Am J Med Genet A. 2020 01; 182(1):250-254.