"Maternal Inheritance" 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.
Transmission of genetic characters, qualities, and traits, solely from maternal extra-nuclear elements such as MITOCHONDRIAL DNA or MATERNAL MESSENGER RNA.
| Descriptor ID |
D000072741
|
| MeSH Number(s) |
G05.420.275.750
|
| Concept/Terms |
Maternal Inheritance- Maternal Inheritance
- Inheritance, Maternal
- Inherited Maternally
- Maternally, Inherited
- Maternally Inherited
- Inherited, Maternally
- Maternal Effect
- Effect, Maternal
- Effects, Maternal
- Maternal Effects
|
Below are MeSH descriptors whose meaning is more general than "Maternal Inheritance".
Below are MeSH descriptors whose meaning is more specific than "Maternal Inheritance".
This graph shows the total number of publications written about "Maternal Inheritance" by people in this website by year, and whether "Maternal Inheritance" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2016 | 0 | 2 | 2 |
| 2017 | 0 | 2 | 2 |
| 2018 | 1 | 1 | 2 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Maternal Inheritance" by people in Profiles.
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Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences. Clin Epigenetics. 2022 03 16; 14(1):41.
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Search for cis-acting factors and maternal effect variants in Silver-Russell patients with ICR1 hypomethylation and their mothers. Eur J Hum Genet. 2019 01; 27(1):42-48.
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Maternal variants in NLRP and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring. J Med Genet. 2018 07; 55(7):497-504.
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Setd1b, encoding a histone 3 lysine 4 methyltransferase, is a maternal effect gene required for the oogenic gene expression program. Development. 2017 07 15; 144(14):2606-2617.
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Maternal uniparental disomy of chromosome 16 [upd(16)mat]: clinical features are rather caused by (hidden) trisomy 16 mosaicism than by upd(16)mat itself. Clin Genet. 2017 Jul; 92(1):45-51.
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Mutation Update for Kabuki Syndrome Genes KMT2D and KDM6A and Further Delineation of X-Linked Kabuki Syndrome Subtype 2. Hum Mutat. 2016 09; 37(9):847-64.
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Genome-wide methylation analysis of retrocopy-associated CpG islands and their genomic environment. Epigenetics. 2016 03 03; 11(3):216-26.
MeSH information
