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Page 1
Fanconi anemia: current insights regarding epidemiology, cancer, and DNA repair.
Peake JD, Noguchi E. Peake JD, et al. Hum Genet. 2022 Dec;141(12):1811-1836. doi: 10.1007/s00439-022-02462-9. Epub 2022 May 21. Hum Genet. 2022. PMID: 35596788 Review.
At least 22 genes are associated with Fanconi anemia, constituting the Fanconi anemia DNA repair pathway. ...Together, the information in this review will underscore important contributions to Fanconi anemia research in the past two decad …
At least 22 genes are associated with Fanconi anemia, constituting the Fanconi anemia DNA repair pathway. ...Tog …
Fanconi Anemia Signaling and Cancer.
Nepal M, Che R, Zhang J, Ma C, Fei P. Nepal M, et al. Trends Cancer. 2017 Dec;3(12):840-856. doi: 10.1016/j.trecan.2017.10.005. Epub 2017 Nov 10. Trends Cancer. 2017. PMID: 29198440 Free PMC article. Review.
The extremely high cancer incidence associated with patients suffering from a rare human genetic disease, Fanconi anemia (FA), demonstrates the importance of FA genes. Over the course of human tumor development, FA genes perform critical tumor-suppression roles. ...
The extremely high cancer incidence associated with patients suffering from a rare human genetic disease, Fanconi anemia (FA), …
Genotype-phenotype associations in Fanconi anemia: A literature review.
Fiesco-Roa MO, Giri N, McReynolds LJ, Best AF, Alter BP. Fiesco-Roa MO, et al. Blood Rev. 2019 Sep;37:100589. doi: 10.1016/j.blre.2019.100589. Epub 2019 Jul 16. Blood Rev. 2019. PMID: 31351673 Free PMC article. Review.
Fanconi anemia (FA) is a genomic instability syndrome with predisposition to congenital abnormalities, bone marrow failure, and cancer. ...We reviewed 187 publications and 1101 cases of FA in which the gene or complementation group was identified and a
Fanconi anemia (FA) is a genomic instability syndrome with predisposition to congenital abnormalities, bone marrow failure, an
The Fanconi anemia pathway and Breast Cancer: A comprehensive review of clinical data.
Gianni P, Matenoglou E, Geropoulos G, Agrawal N, Adnani H, Zafeiropoulos S, Miyara SJ, Guevara S, Mumford JM, Molmenti EP, Giannis D. Gianni P, et al. Clin Breast Cancer. 2022 Jan;22(1):10-25. doi: 10.1016/j.clbc.2021.08.001. Epub 2021 Aug 10. Clin Breast Cancer. 2022. PMID: 34489172 Review.
Dysregulation of the DNA damage response causes genomic instability and increases the rate of mutagenesis and the risk of carcinogenesis. The Fanconi Anemia (FA) pathway is an important component of the DNA damage response and plays a critical role in the repair of …
Dysregulation of the DNA damage response causes genomic instability and increases the rate of mutagenesis and the risk of carcinogenesis. Th …
[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. ...
Fanconi anemia (FA) is a genetic disorder characterized by progressive bone marrow failure, increased susceptibility to leukem
Multifaceted Fanconi Anemia Signaling.
Che R, Zhang J, Nepal M, Han B, Fei P. Che R, et al. Trends Genet. 2018 Mar;34(3):171-183. doi: 10.1016/j.tig.2017.11.006. Epub 2017 Dec 16. Trends Genet. 2018. PMID: 29254745 Free PMC article. Review.
In 1927 Guido Fanconi described a hereditary condition presenting panmyelopathy accompanied by short stature and hyperpigmentation, now better known as Fanconi anemia (FA). ...
In 1927 Guido Fanconi described a hereditary condition presenting panmyelopathy accompanied by short stature and hyperpigmentation, n …
Type-I Interferon Signaling in Fanconi Anemia.
Landelouci K, Sinha S, Pépin G. Landelouci K, et al. Front Cell Infect Microbiol. 2022 Feb 7;12:820273. doi: 10.3389/fcimb.2022.820273. eCollection 2022. Front Cell Infect Microbiol. 2022. PMID: 35198459 Free PMC article. Review.
Fanconi Anemia (FA) is a genome instability syndrome caused by mutations in one of the 23 repair genes of the Fanconi pathway. ...A better understanding of the molecular mechanisms engaging type-I Interferon signaling in FA may ultimately lead to the discover
Fanconi Anemia (FA) is a genome instability syndrome caused by mutations in one of the 23 repair genes of the Fanconi p
Fanconi anemia.
Green AM, Kupfer GM. Green AM, et al. Hematol Oncol Clin North Am. 2009 Apr;23(2):193-214. doi: 10.1016/j.hoc.2009.01.008. Hematol Oncol Clin North Am. 2009. PMID: 19327579 Free PMC article. Review.
Fanconi anemia (FA) is an autosomal and X-linked recessive disorder characterized by bone marrow failure, acute myelogenous leukemia, solid tumors, and developmental abnormalities. ...
Fanconi anemia (FA) is an autosomal and X-linked recessive disorder characterized by bone marrow failure, acute myelogenous le
245 results