Fanconi Anemia Complementation Group A Protein
"Fanconi Anemia Complementation Group A 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 is the most commonly mutated protein in FANCONI ANEMIA. It undergoes PHOSPHORYLATION by PROTEIN KINASE B and forms a complex with FANCC PROTEIN in the CELL NUCLEUS.
| Descriptor ID |
D052217
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| MeSH Number(s) |
D12.776.313.500 D12.776.660.264 D12.776.744.476
|
| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Fanconi Anemia Complementation Group A Protein".
Below are MeSH descriptors whose meaning is more specific than "Fanconi Anemia Complementation Group A Protein".
This graph shows the total number of publications written about "Fanconi Anemia Complementation Group A Protein" by people in this website by year, and whether "Fanconi Anemia Complementation Group A Protein" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 0 | 1 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Fanconi Anemia Complementation Group A Protein" by people in Profiles.
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Amelioration of Mucositis in Proton Therapy of Fanconi Anemia Fanca-/- Mice by JP4-039. In Vivo. 2019 Nov-Dec; 33(6):1757-1766.
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Continuous One Year Oral Administration of the Radiation Mitigator, MMS350, after Total-Body Irradiation, Restores Bone Marrow Stromal Cell Proliferative Capacity and Reduces Senescence in Fanconi Anemia (Fanca-/-) Mice. Radiat Res. 2019 02; 191(2):139-153.
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Preimplantation HLA typing with aneuploidy testing. Reprod Biomed Online. 2006 Jan; 12(1):89-100.
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Acquired FANCA dysfunction and cytogenetic instability in adult acute myelogenous leukemia. Blood. 2003 Jul 01; 102(1):7-16.