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Year Number of Results
1998 1
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2009 4
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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 pr …
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 …
Regulation of R-loops and genome instability in Fanconi anemia.
Okamoto Y, Hejna J, Takata M. Okamoto Y, et al. J Biochem. 2019 Jun 1;165(6):465-470. doi: 10.1093/jb/mvz019. J Biochem. 2019. PMID: 30821334 Review.
Fanconi anemia (FA) is a devastating hereditary disorder with impaired genome stability resulting in physical abnormalities, gradual loss of hematopoietic stem cells and development of tumours and leukaemia. ...
Fanconi anemia (FA) is a devastating hereditary disorder with impaired genome stability resulting in physical abnormalities, g …
Fanconi anemia and ubiquitination.
Zhang Y, Zhou X, Huang P. Zhang Y, et al. J Genet Genomics. 2007 Jul;34(7):573-80. doi: 10.1016/S1673-8527(07)60065-4. J Genet Genomics. 2007. PMID: 17643942 Review.
Fanconi anemia (FA) is a rare recessive hereditary disease characterized clinically by congenital defects, progressive bone-marrow failure, and cancer predisposition. ...
Fanconi anemia (FA) is a rare recessive hereditary disease characterized clinically by congenital defects, progressive bone-ma …
Interplay between Fanconi anemia and homologous recombination pathways in genome integrity.
Michl J, Zimmer J, Tarsounas M. Michl J, et al. EMBO J. 2016 May 2;35(9):909-23. doi: 10.15252/embj.201693860. Epub 2016 Apr 1. EMBO J. 2016. PMID: 27037238 Free PMC article. Review.
The Fanconi anemia (FA) pathway plays a central role in the repair of DNA interstrand crosslinks (ICLs) and regulates cellular responses to replication stress. ...Consistent with this, rare patient mutations in these HR genes cause FA pathologies and have been assig …
The Fanconi anemia (FA) pathway plays a central role in the repair of DNA interstrand crosslinks (ICLs) and regulates cellular …
Emerging functions of the Fanconi anemia pathway at a glance.
Sumpter R Jr, Levine B. Sumpter R Jr, et al. J Cell Sci. 2017 Aug 15;130(16):2657-2662. doi: 10.1242/jcs.204909. J Cell Sci. 2017. PMID: 28811338 Free PMC article. Review.
Fanconi anemia (FA) is a rare disease, in which homozygous or compound heterozygous inactivating mutations in any of 21 genes lead to genomic instability, early-onset bone marrow failure and increased cancer risk. ...
Fanconi anemia (FA) is a rare disease, in which homozygous or compound heterozygous inactivating mutations in any of 21 genes …
Fanconi anemia: a signal transduction and DNA repair pathway.
Kupfer GM. Kupfer GM. Yale J Biol Med. 2013 Dec 13;86(4):491-7. Yale J Biol Med. 2013. PMID: 24348213 Free PMC article. Review.
Fanconi anemia (FA) is a fascinating, rare genetic disorder marked by congenital defects, bone marrow failure, and cancer susceptibility. ...
Fanconi anemia (FA) is a fascinating, rare genetic disorder marked by congenital defects, bone marrow failure, and cancer susc …
Fanconi anemia and DNA replication repair.
Patel KJ, Joenje H. Patel KJ, et al. DNA Repair (Amst). 2007 Jul 1;6(7):885-90. doi: 10.1016/j.dnarep.2007.02.002. Epub 2007 May 3. DNA Repair (Amst). 2007. PMID: 17481966 Review.
Kennedy, A.D. D'Andrea, The Fanconi anemia/BRCA pathway: new faces in the crowd, Genes Dev. 19 (2005) 2925-2940; L.J. Niedernhofer, A.S. Lalai, J.H. Hoeijmakers, Fanconi anemia (cross)linked to DNA repair, Cell 123 (2005) 1191-1198; H. .. …
Kennedy, A.D. D'Andrea, The Fanconi anemia/BRCA pathway: new faces in the crowd, Genes Dev. 19 (2005) 2925-2940; L.J. N …
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. ...
The Role of PALB2 in the DNA Damage Response and Cancer Predisposition.
Nepomuceno TC, De Gregoriis G, de Oliveira FMB, Suarez-Kurtz G, Monteiro AN, Carvalho MA. Nepomuceno TC, et al. Int J Mol Sci. 2017 Aug 31;18(9):1886. doi: 10.3390/ijms18091886. Int J Mol Sci. 2017. PMID: 28858227 Free PMC article. Review.
PALB2 (Partner and Localizer of Breast Cancer 2 (BRCA2)) plays an important role in maintaining genome integrity through its role in the Fanconi anemia (FA) and homologous recombination (HR) DNA repair pathways. ...
PALB2 (Partner and Localizer of Breast Cancer 2 (BRCA2)) plays an important role in maintaining genome integrity through its role in the …
46 results