"Genomic Imprinting" 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 variable phenotypic expression of a GENE depending on whether it is of paternal or maternal origin, which is a function of the DNA METHYLATION pattern. Imprinted regions are observed to be more methylated and less transcriptionally active. (Segen, Dictionary of Modern Medicine, 1992)
| Descriptor ID |
D018392
|
| MeSH Number(s) |
G05.308.203.500
|
| Concept/Terms |
Genomic Imprinting- Genomic Imprinting
- Imprinting, Genomic
- Parental Imprinting
- Imprinting, Parental
- Imprinting, Genetic
- Genetic Imprinting
|
Below are MeSH descriptors whose meaning is more general than "Genomic Imprinting".
Below are MeSH descriptors whose meaning is more specific than "Genomic Imprinting".
This graph shows the total number of publications written about "Genomic Imprinting" by people in this website by year, and whether "Genomic Imprinting" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 0 | 1 | 1 |
| 2008 | 0 | 1 | 1 |
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Below are the most recent publications written about "Genomic Imprinting" by people in Profiles.
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CTCF-dependent chromatin bias constitutes transient epigenetic memory of the mother at the H19-Igf2 imprinting control region in prospermatogonia. PLoS Genet. 2010 Nov 24; 6(11):e1001224.
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Genetic and epigenetic factors at COL2A1 and ABCA4 influence clinical outcome in congenital toxoplasmosis. PLoS One. 2008 Jun 04; 3(6):e2285.
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Maternal inheritance and chromosome 18 allele sharing in unilineal bipolar illness pedigrees. Am J Med Genet. 1996 Apr 09; 67(2):202-7.