Heterogeneous-Nuclear Ribonucleoprotein U
"Heterogeneous-Nuclear Ribonucleoprotein U" 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.
A heterogeneous-nuclear ribonucleoprotein found associated with the NUCLEAR MATRIX.
| Descriptor ID |
D034722
|
| MeSH Number(s) |
D12.776.157.725.813.750.800 D12.776.660.650.500 D12.776.664.962.813.750.800
|
| Concept/Terms |
Heterogeneous-Nuclear Ribonucleoprotein U- Heterogeneous-Nuclear Ribonucleoprotein U
- Heterogeneous Nuclear Ribonucleoprotein U
- Ribonucleoprotein U, Heterogeneous-Nuclear
- Scaffold Attachment Factor A (SAF-A)
- hnRNP U
- Glucocorticoid Receptor Interacting Protein 120
- GRIP120
|
Below are MeSH descriptors whose meaning is more general than "Heterogeneous-Nuclear Ribonucleoprotein U".
Below are MeSH descriptors whose meaning is more specific than "Heterogeneous-Nuclear Ribonucleoprotein U".
This graph shows the total number of publications written about "Heterogeneous-Nuclear Ribonucleoprotein U" by people in this website by year, and whether "Heterogeneous-Nuclear Ribonucleoprotein U" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2005 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2020 | 0 | 1 | 1 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Heterogeneous-Nuclear Ribonucleoprotein U" by people in Profiles.
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Expanding the phenotype of HNRNPU-related neurodevelopmental disorder with emphasis on seizure phenotype and review of literature. Am J Med Genet A. 2022 05; 188(5):1497-1514.
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Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders. Nat Commun. 2020 10 01; 11(1):4932.
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FANCD2 protects genome stability by recruiting RNA processing enzymes to resolve R-loops during mild replication stress. FEBS J. 2019 01; 286(1):139-150.
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Clinical and molecular characterization of de novo loss of function variants in HNRNPU. Am J Med Genet A. 2017 Oct; 173(10):2680-2689.
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Cloning and characterization of cDNAs expressed during chick development and encoding different isoforms of a putative zinc finger transcriptional regulator. Biochimie. 2005 Nov; 87(11):939-49.