"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 | 1 | 0 | 1 |
| 1997 | 2 | 1 | 3 |
| 2002 | 1 | 0 | 1 |
| 2004 | 0 | 1 | 1 |
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Below are the most recent publications written about "X Chromosome" by people in Profiles.
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Ng D, Thakker N, Corcoran CM, Donnai D, Perveen R, Schneider A, Hadley DW, Tifft C, Zhang L, Wilkie AO, van der Smagt JJ, Gorlin RJ, Burgess SM, Bardwell VJ, Black GC, Biesecker LG. Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR. Nat Genet. 2004 Apr; 36(4):411-6.
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Ganesan S, Silver DP, Greenberg RA, Avni D, Drapkin R, Miron A, Mok SC, Randrianarison V, Brodie S, Salstrom J, Rasmussen TP, Klimke A, Marrese C, Marahrens Y, Deng CX, Feunteun J, Livingston DM. BRCA1 supports XIST RNA concentration on the inactive X chromosome. Cell. 2002 Nov 01; 111(3):393-405.
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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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Regillo CD, Custis PH. Surgical management of retinoschisis. Curr Opin Ophthalmol. 1997 Jun; 8(3):80-6.
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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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Iyer GS, Krahe R, Goodwin LA, Doggett NA, Siciliano MJ, Funanage VL, Proujansky R. Identification of a testis-expressed creatine transporter gene at 16p11.2 and confirmation of the X-linked locus to Xq28. Genomics. 1996 May 15; 34(1):143-6.
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Regillo CD, Tasman WS, Brown GC. Surgical management of complications associated with X-linked retinoschisis. Arch Ophthalmol. 1993 Aug; 111(8):1080-6.