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[Fanconi anemia].
Yamashita T. Yamashita T. Rinsho Ketsueki. 2019;60(5):403-407. doi: 10.11406/rinketsu.60.403. Rinsho Ketsueki. 2019. PMID: 31168005 Review. Japanese.
Fanconi anemia (FA) is a genetic disorder characterized by progressive bone marrow failure, increased susceptibility to leukemia and cancer, and genomic instabilities. Protein products encoded by 22 FA genes, identified till date, cooperate in a molecular pathway ca …
Fanconi anemia (FA) is a genetic disorder characterized by progressive bone marrow failure, increased susceptibility to leukem …
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. Cells from FA patients exhibit hypersensitivity to DNA cross-linking agents, such as mitomycin C …
Fanconi anemia (FA) is a rare recessive hereditary disease characterized clinically by congenital defects, progressive bone-ma …
Familial pancreatic cancer.
Petersen GM. Petersen GM. Semin Oncol. 2016 Oct;43(5):548-553. doi: 10.1053/j.seminoncol.2016.09.002. Epub 2016 Sep 22. Semin Oncol. 2016. PMID: 27899186 Free PMC article. Review.
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 bone marro …
Fanconi anemia (FA) is an autosomal recessive disorder caused by defects in at least eight distinct genes FANCA, B, C, …
Fanconi anemia: current management.
Kook H. Kook H. Hematology. 2005;10 Suppl 1:108-10. doi: 10.1080/10245330512331390096. Hematology. 2005. PMID: 16188650 Review.
All racial and ethnic groups are at risk, and at least 11 complementation groups have been identified and the genes defective in eight of these have been identified (FANCA, C, D2, E, F, G, L and BRCA2). FA-A is the most common complementation group, ac …
All racial and ethnic groups are at risk, and at least 11 complementation groups have been identified and the genes defective in eigh …
Advances in Gene Therapy for Fanconi Anemia.
Río P, Navarro S, Bueren JA. Río P, et al. Hum Gene Ther. 2018 Oct;29(10):1114-1123. doi: 10.1089/hum.2018.124. Hum Gene Ther. 2018. PMID: 30117331 Review.
Fanconi anemia (FA) is a rare inherited disease that is associated with bone marrow failure and a predisposition to cancer. ...
Fanconi anemia (FA) is a rare inherited disease that is associated with bone marrow failure and a predisposition to cancer. .. …
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 …
Fanconi anemia: causes and consequences of genetic instability.
Kalb R, Neveling K, Nanda I, Schindler D, Hoehn H. Kalb R, et al. Genome Dyn. 2006;1:218-242. doi: 10.1159/000092510. Genome Dyn. 2006. PMID: 18724063 Review.
Fanconi anemia (FA) is a rare recessive disease that reflects the cellular and phenotypic consequences of genetic instability: growth retardation, congenital malformations, bone marrow failure, high risk of neoplasia, and premature aging. ...In fact, only leaky or h …
Fanconi anemia (FA) is a rare recessive disease that reflects the cellular and phenotypic consequences of genetic instability: …
Fanconi anemia in Ashkenazi Jews.
Kutler DI, Auerbach AD. Kutler DI, et al. Fam Cancer. 2004;3(3-4):241-8. doi: 10.1007/s10689-004-9565-8. Fam Cancer. 2004. PMID: 15516848 Review.
While patients may be from widely diverse ethnic groups, a single mutation in complementation group FA-C, c.711 + 4A > T (commonly known as IVS4 + 4A > T prior to current nomenclature rules) is unique to FA patients of Ashkenazi Jewish ancestry, …
While patients may be from widely diverse ethnic groups, a single mutation in complementation group FA-C, c.711 …
Cellular and molecular consequences of defective Fanconi anemia proteins in replication-coupled DNA repair: mechanistic insights.
Thompson LH, Hinz JM. Thompson LH, et al. Mutat Res. 2009 Jul 31;668(1-2):54-72. doi: 10.1016/j.mrfmmm.2009.02.003. Epub 2009 Feb 21. Mutat Res. 2009. PMID: 19622404 Free PMC article. Review.
The Fanconi anemia (FA) molecular network consists of 15 "FANC" proteins, of which 13 are associated with mutations in patients with this cancer-prone chromosome instability disorder. ...The FANC core subcomplex (FANCA, B, C, E, F, G, L, FAAP100) promotes TLS …
The Fanconi anemia (FA) molecular network consists of 15 "FANC" proteins, of which 13 are associated with mutations in patient …
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