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

Year Number of Results
1946 5
1947 4
1948 3
1949 4
1950 4
1951 4
1952 13
1953 12
1954 5
1955 8
1956 2
1957 7
1958 8
1959 6
1960 4
1961 11
1962 10
1963 12
1964 15
1965 15
1966 7
1967 14
1968 7
1969 13
1970 11
1971 15
1972 19
1973 13
1974 17
1975 31
1976 35
1977 51
1978 38
1979 33
1980 49
1981 44
1982 46
1983 53
1984 42
1985 47
1986 40
1987 41
1988 29
1989 46
1990 34
1991 54
1992 60
1993 91
1994 72
1995 76
1996 101
1997 89
1998 103
1999 86
2000 104
2001 120
2002 103
2003 136
2004 144
2005 142
2006 156
2007 171
2008 182
2009 207
2010 219
2011 237
2012 248
2013 271
2014 290
2015 307
2016 337
2017 285
2018 271
2019 256
2020 322
2021 332
2022 272
2023 287
2024 284
2025 272

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6,975 results

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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. This pathway coordinates multiple processes and proteins to facilitate the repair of DNA adducts including interstrand crosslinks (ICLs) that are …
At least 22 genes are associated with Fanconi anemia, constituting the Fanconi anemia DNA repair pathway. This 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
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 …
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. ...
Among human genetic diseases, Fanconi Anemia (FA) tops all with its largest number of health complications in nearly all human …
Fanconi's anemia. Current concepts.
Alter BP. Alter BP. Am J Pediatr Hematol Oncol. 1992 May;14(2):170-6. Am J Pediatr Hematol Oncol. 1992. PMID: 1530123 Review.
Fanconi's anemia is an autosomal recessive disorder with a high incidence (greater than 90%) of aplastic anemia and a premalignant component with a greater than 10% risk of leukemia or solid tumors. ...Not every patient has a poor prognosis. There are now man
Fanconi's anemia is an autosomal recessive disorder with a high incidence (greater than 90%) of aplastic anemia and a p
Fanconi anemia proteins in telomere maintenance.
Sarkar J, Liu Y. Sarkar J, et al. DNA Repair (Amst). 2016 Jul;43:107-12. doi: 10.1016/j.dnarep.2016.02.007. Epub 2016 Apr 8. DNA Repair (Amst). 2016. PMID: 27118469 Free PMC article. Review.
Here we discuss telomere abnormalities in a rare recessive chromosomal instability disorder called Fanconi Anemia and the role of the Fanconi Anemia pathway in telomere biology. Reports suggest that Fanconi Anemia proteins play a role in …
Here we discuss telomere abnormalities in a rare recessive chromosomal instability disorder called Fanconi Anemia and the role …
Fanconi anemia (cross)linked to DNA repair.
Niedernhofer LJ, Lalai AS, Hoeijmakers JH. Niedernhofer LJ, et al. Cell. 2005 Dec 29;123(7):1191-8. doi: 10.1016/j.cell.2005.12.009. Cell. 2005. PMID: 16377561 Free article. Review.
Fanconi anemia is characterized by hypersensitivity to DNA interstrand crosslinks (ICLs) and susceptibility to tumor formation. Despite the identification of numerous Fanconi anemia (FANC) genes, the mechanism by which proteins encoded by these genes p
Fanconi anemia is characterized by hypersensitivity to DNA interstrand crosslinks (ICLs) and susceptibility to tumor formation
6,975 results