Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1990 1
1994 1
1995 1
1997 2
1998 3
1999 3
2001 3
2002 4
2003 5
2004 3
2005 6
2006 8
2007 6
2008 6
2009 10
2010 7
2011 8
2012 5
2013 6
2014 10
2015 4
2016 10
2017 7
2018 5
2019 1
2020 6
2021 9
2022 6
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

129 results

Results by year

Filters applied: . Clear all
Your search was processed without automatic term mapping because it retrieved zero results.
Page 1
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
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
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 …
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), …
Fanconi anemia.
Bagby GC, Alter BP. Bagby GC, et al. Semin Hematol. 2006 Jul;43(3):147-56. doi: 10.1053/j.seminhematol.2006.04.005. Semin Hematol. 2006. PMID: 16822457 Review.
Fanconi anemia (FA) is a rare hereditary disease characterized by bone marrow failure and developmental anomalies; a high incidence of myelodysplasia (MDS), acute nonlymphocytic leukemia (AML), and solid tumors; and cellular hypersensitivity to cross-linking agents.
Fanconi anemia (FA) is a rare hereditary disease characterized by bone marrow failure and developmental anomalies; a high inci
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 anemia proteins and genome fragility: unraveling replication defects for cancer therapy.
Badra Fajardo N, Taraviras S, Lygerou Z. Badra Fajardo N, et al. Trends Cancer. 2022 Jun;8(6):467-481. doi: 10.1016/j.trecan.2022.01.015. Epub 2022 Feb 26. Trends Cancer. 2022. PMID: 35232683 Review.
Accurate and complete genome duplication is crucial to maintain cell survival and prevent malignant transformation. The Fanconi anemia (FA) pathway has traditionally been associated with the repair of DNA interstrand crosslinks that impede the progression of the rep …
Accurate and complete genome duplication is crucial to maintain cell survival and prevent malignant transformation. The Fanconi an
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 homeost
Fanconi anaemia (FA) is a genetic disorder that is characterized by bone marrow failure (BMF), developmental abnormalities and predis
129 results