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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2001 2
2002 3
2003 4
2004 4
2005 4
2006 1
2008 2
2009 4
2010 2
2013 3
2014 5
2016 1
2017 4
2018 3
2020 2
2021 5
2022 1
2024 0

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44 results

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Page 1
FANCD2 and DNA Damage.
Nepal M, Che R, Ma C, Zhang J, Fei P. Nepal M, et al. Int J Mol Sci. 2017 Aug 19;18(8):1804. doi: 10.3390/ijms18081804. Int J Mol Sci. 2017. PMID: 28825622 Free PMC article. Review.
Investigators have dedicated considerable effort to understanding the molecular basis underlying Fanconi Anemia (FA), a rare human genetic disease featuring an extremely high incidence of cancer and many congenital defects. Among those studies, FA group D2 …
Investigators have dedicated considerable effort to understanding the molecular basis underlying Fanconi Anemia (FA), a rare h …
Focal Point of Fanconi Anemia Signaling.
Zhan S, Siu J, Wang Z, Yu H, Bezabeh T, Deng Y, Du W, Fei P. Zhan S, et al. Int J Mol Sci. 2021 Nov 30;22(23):12976. doi: 10.3390/ijms222312976. Int J Mol Sci. 2021. PMID: 34884777 Free PMC article. Review.
Among human genetic diseases, Fanconi Anemia (FA) tops all with its largest number of health complications in nearly all human organ systems, suggesting the significant roles played by FA genes in the maintenance of human health. With the accumulated research on FA, …
Among human genetic diseases, Fanconi Anemia (FA) tops all with its largest number of health complications in nearly all human …
Structural insight into FANCI-FANCD2 monoubiquitination.
Li L, Tan W, Deans AJ. Li L, et al. Essays Biochem. 2020 Oct 26;64(5):807-817. doi: 10.1042/EBC20200001. Essays Biochem. 2020. PMID: 32725171 Free PMC article. Review.
The Fanconi anemia (FA) pathway coordinates a faithful repair mechanism for DNA damage that blocks DNA replication, such as interstrand cross-links. ...
The Fanconi anemia (FA) pathway coordinates a faithful repair mechanism for DNA damage that blocks DNA replication, such as in …
Fanconi anaemia and cancer: an intricate relationship.
Nalepa G, Clapp DW. Nalepa G, et al. Nat Rev Cancer. 2018 Mar;18(3):168-185. doi: 10.1038/nrc.2017.116. Epub 2018 Jan 29. Nat Rev Cancer. 2018. PMID: 29376519 Review.
Fanconi anaemia (FA) is a genetic disorder that is characterized by bone marrow failure (BMF), developmental abnormalities and predisposition to cancer. Together with other proteins involved in DNA repair processes and cell division, the FA proteins maintain genome …
Fanconi anaemia (FA) is a genetic disorder that is characterized by bone marrow failure (BMF), developmental abnormalities and …
Regulation of the Fanconi Anemia DNA Repair Pathway by Phosphorylation and Monoubiquitination.
Ishiai M. Ishiai M. Genes (Basel). 2021 Nov 5;12(11):1763. doi: 10.3390/genes12111763. Genes (Basel). 2021. PMID: 34828369 Free PMC article. Review.
The Fanconi anemia (FA) DNA repair pathway coordinates a faithful repair mechanism for stalled DNA replication forks caused by factors such as DNA interstrand crosslinks (ICLs) or replication stress. ...
The Fanconi anemia (FA) DNA repair pathway coordinates a faithful repair mechanism for stalled DNA replication forks caused by …
Fanconi anemia: current management.
Kook H. Kook H. Hematology. 2005;10 Suppl 1:108-10. doi: 10.1080/10245330512331390096. Hematology. 2005. PMID: 16188650 Review.
Fanconi anemia (FA) is an autosomal recessive chromosomal instability disorder, characterized by congenital anomalies, defective hematopoiesis and a high risk of developing acute myeloid leukemia and certain solid tumors. All racial and ethnic groups are at r …
Fanconi anemia (FA) is an autosomal recessive chromosomal instability disorder, characterized by congenital anomalies, defecti …
Mechanism, specificity, and function of FANCD2-FANCI ubiquitination and deubiquitination.
Lemonidis K, Arkinson C, Rennie ML, Walden H. Lemonidis K, et al. FEBS J. 2022 Aug;289(16):4811-4829. doi: 10.1111/febs.16077. Epub 2021 Jun 29. FEBS J. 2022. PMID: 34137174 Free article. Review.
Fanconi anemia (FA) is a rare genetic disorder caused by mutations in any of the currently 22 known FA genes. ...
Fanconi anemia (FA) is a rare genetic disorder caused by mutations in any of the currently 22 known FA genes. ...
Fanconi anemia and DNA repair.
Grompe M, D'Andrea A. Grompe M, et al. Hum Mol Genet. 2001 Oct 1;10(20):2253-9. doi: 10.1093/hmg/10.20.2253. Hum Mol Genet. 2001. PMID: 11673408 Review.
Fanconi anemia (FA) is an autosomal recessive disorder caused by defects in at least eight distinct genes FANCA, B, C, D1, D2, E, F and G. The clinical phenotype of all FA complementation groups is similar and is characterized by progressive bon …
Fanconi anemia (FA) is an autosomal recessive disorder caused by defects in at least eight distinct genes FANCA, B, C, D1, …
The Fanconi anemia ID2 complex: dueling saxes at the crossroads.
Boisvert RA, Howlett NG. Boisvert RA, et al. Cell Cycle. 2014;13(19):2999-3015. doi: 10.4161/15384101.2014.956475. Cell Cycle. 2014. PMID: 25486561 Free PMC article. Review.
Fanconi anemia (FA) is a rare recessive genetic disease characterized by congenital abnormalities, bone marrow failure and heightened cancer susceptibility in early adulthood. ...
Fanconi anemia (FA) is a rare recessive genetic disease characterized by congenital abnormalities, bone marrow failure and hei …
The ubiquitination machinery of the Fanconi Anemia DNA repair pathway.
Tan W, Deans AJ. Tan W, et al. Prog Biophys Mol Biol. 2021 Aug;163:5-13. doi: 10.1016/j.pbiomolbio.2020.09.009. Epub 2020 Oct 12. Prog Biophys Mol Biol. 2021. PMID: 33058944 Review.
The Fanconi Anemia (FA) pathway maintains genome stability by preventing DNA damage from occurring when replication is blocked. ...
The Fanconi Anemia (FA) pathway maintains genome stability by preventing DNA damage from occurring when replication is blocked …
44 results