"X Chromosome" 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 female sex chromosome, being the differential sex chromosome carried by half the male gametes and all female gametes in human and other male-heterogametic species.
| Descriptor ID |
D014960
|
| MeSH Number(s) |
A11.284.187.865.982 G05.360.162.865.982
|
| Concept/Terms |
X Chromosome- X Chromosome
- Chromosome, X
- Chromosomes, X
- X Chromosomes
|
Below are MeSH descriptors whose meaning is more general than "X Chromosome".
Below are MeSH descriptors whose meaning is more specific than "X Chromosome".
This graph shows the total number of publications written about "X Chromosome" by people in this website by year, and whether "X Chromosome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 2 | 1 | 3 |
| 1997 | 1 | 1 | 2 |
| 1998 | 1 | 2 | 3 |
| 1999 | 0 | 2 | 2 |
| 2000 | 1 | 0 | 1 |
| 2025 | 1 | 0 | 1 |
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Below are the most recent publications written about "X Chromosome" by people in Profiles.
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Sierra I, Toothacre NE, van der Weide RH, Lovell CD, Nguyen SC, Barnett RJ, Cook AL, Ryu HS, Pyfrom S, Wang H, Beiting D, Philips-Cremins JE, Joyce EF, Anguera MC. B cell stimulation changes the structure and higher-order organization of the inactive X chromosome. Cell Rep. 2025 Mar 25; 44(3):115351.
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Tao L, Boyd M, Gonye G, Malone B, Schwaber J. BTK mutations in patients with X-linked agammaglobulinemia: lack of correlation between presence of peripheral B lymphocytes and specific mutations. Hum Mutat. 2000 Dec; 16(6):528-9.
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Melhem ER, Barker PB, Raymond GV, Moser HW. X-linked adrenoleukodystrophy in children: review of genetic, clinical, and MR imaging characteristics. AJR Am J Roentgenol. 1999 Dec; 173(6):1575-81.
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Fischbeck KH, Lieberman A, Bailey CK, Abel A, Merry DE. Androgen receptor mutation in Kennedy's disease. Philos Trans R Soc Lond B Biol Sci. 1999 Jun 29; 354(1386):1075-8.
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Dube JL, Wang P, Elvin J, Lyons KM, Celeste AJ, Matzuk MM. The bone morphogenetic protein 15 gene is X-linked and expressed in oocytes. Mol Endocrinol. 1998 Dec; 12(12):1809-17.
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Merry DE, Kobayashi Y, Bailey CK, Taye AA, Fischbeck KH. Cleavage, aggregation and toxicity of the expanded androgen receptor in spinal and bulbar muscular atrophy. Hum Mol Genet. 1998 Apr; 7(4):693-701.
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Kiuru-Kuhlefelt S, El-Rifai W, Sarlomo-Rikala M, Knuutila S, Miettinen M. DNA copy number changes in alveolar soft part sarcoma: a comparative genomic hybridization study. Mod Pathol. 1998 Mar; 11(3):227-31.
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Johnston J, Kelley RI, Feigenbaum A, Cox GF, Iyer GS, Funanage VL, Proujansky R. Mutation characterization and genotype-phenotype correlation in Barth syndrome. Am J Hum Genet. 1997 Nov; 61(5):1053-8.
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Fortina P, Cheng J, Shoffner MA, Surrey S, Hitchcock WM, Kricka LJ, Wilding P. Diagnosis of Duchenne/Becker muscular dystrophy and quantitative identification of carrier status by use of entangled solution capillary electrophoresis. Clin Chem. 1997 May; 43(5):745-51.
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Inoue K, Suzuki Y, Yajima S, Shimozawa N, Tomatsu S, Orii T, Kondo N. Carrier identification of X-linked adrenoleukodystrophy by measurement of very long chain fatty acids and lignoceric acid oxidation. Clin Genet. 1996 Nov; 50(5):348-52.