Fanconi Anemia Complementation Group G Protein
"Fanconi Anemia Complementation Group G Protein" 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 Fanconi anemia complementation group protein that undergoes PHOSPHORYLATION by CDC2 PROTEIN KINASE during MITOSIS. It forms a complex with other FANCONI ANEMIA PROTEINS and helps protect CELLS from DNA DAMAGE by genotoxic agents.
| Descriptor ID |
D052241
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| MeSH Number(s) |
D12.776.313.906 D12.776.744.488
|
| Concept/Terms |
Fanconi Anemia Complementation Group G Protein- Fanconi Anemia Complementation Group G Protein
- XRCC9 Protein
- Fanconi Anemia Group G Protein
- X-Ray Repair Complementing Defective Repair In Chinese Hamster Cells 9 Protein
- X Ray Repair Complementing Defective Repair In Chinese Hamster Cells 9 Protein
- FANCG Protein
- Fanconi Anemia Group G Complementing Protein
|
Below are MeSH descriptors whose meaning is more general than "Fanconi Anemia Complementation Group G Protein".
Below are MeSH descriptors whose meaning is more specific than "Fanconi Anemia Complementation Group G Protein".
This graph shows the total number of publications written about "Fanconi Anemia Complementation Group G Protein" by people in this website by year, and whether "Fanconi Anemia Complementation Group G Protein" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2005 | 0 | 1 | 1 |
| 2013 | 2 | 0 | 2 |
| 2014 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
| 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Fanconi Anemia Complementation Group G Protein" by people in Profiles.
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Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation. Mol Genet Genomic Med. 2020 08; 8(8):e1351.
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Diagnosis of Fanconi Anaemia by ionising radiation- or mitomycin C-induced micronuclei. DNA Repair (Amst). 2018 01; 61:17-24.
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Hematological consequences of a FANCG founder mutation in Black South African patients with Fanconi anemia. Blood Cells Mol Dis. 2015 Mar; 54(3):270-4.
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Phenotypic consequences in black South African Fanconi anemia patients homozygous for a founder mutation. Genet Med. 2014 May; 16(5):400-6.
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Fanconi anaemia in black South African patients heterozygous for the FANCG c.637-643delTACCGCC founder mutation. S Afr Med J. 2013 Oct 11; 103(12 Suppl 1):970-3.
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A common Fanconi anemia mutation in black populations of sub-Saharan Africa. Blood. 2005 May 01; 105(9):3542-4.