"Genes, X-Linked" 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.
Genes that are located on the X CHROMOSOME.
| Descriptor ID |
D050172
|
| MeSH Number(s) |
G05.360.340.024.340.500 G05.420.457
|
| Concept/Terms |
Genes, X-Linked- Genes, X-Linked
- Genes, X Linked
- Genes, X-Chromosome
- Gene, X-Chromosome
- Genes, X Chromosome
- X-Chromosome Gene
- X-Chromosome Genes
- X Chromosome Genes
- X-Linked Genes
- Gene, X-Linked
- X Linked Genes
- X-Linked Gene
Alleles, X-Linked- Alleles, X-Linked
- Allele, X-Linked
- Alleles, X Linked
- X-Linked Allele
- X-Linked Alleles
X-Linked Traits- X-Linked Traits
- Trait, X-Linked
- X Linked Traits
- X-Linked Trait
- Traits, X-Linked
- Traits, X Linked
|
Below are MeSH descriptors whose meaning is more general than "Genes, X-Linked".
Below are MeSH descriptors whose meaning is more specific than "Genes, X-Linked".
This graph shows the total number of publications written about "Genes, X-Linked" by people in this website by year, and whether "Genes, X-Linked" 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 |
|---|
| 2012 | 1 | 0 | 1 |
| 2013 | 0 | 2 | 2 |
| 2015 | 0 | 2 | 2 |
| 2021 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Genes, X-Linked" by people in Profiles.
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Increased p53 signaling impairs neural differentiation in HUWE1-promoted intellectual disabilities. Cell Rep Med. 2021 04 20; 2(4):100240.
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ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneurons. Hum Mol Genet. 2015 Sep 01; 24(17):4848-61.
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Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity. Hum Mol Genet. 2015 May 15; 24(10):2861-72.
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A Y328C missense mutation in spermine synthase causes a mild form of Snyder-Robinson syndrome. Hum Mol Genet. 2013 Sep 15; 22(18):3789-97.
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A rational free energy-based approach to understanding and targeting disease-causing missense mutations. J Am Med Inform Assoc. 2013 Jul-Aug; 20(4):643-51.
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X chromosome gene methylation in peripheral lymphocytes from monozygotic twins discordant for scleroderma. Clin Exp Immunol. 2012 Sep; 169(3):253-62.