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Year Number of Results
2001 2
2002 1
2003 3
2004 2
2005 4
2006 2
2008 2
2009 3
2014 1
2016 1
2021 1
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Page 1
G-quadruplexes and helicases.
Mendoza O, Bourdoncle A, Boulé JB, Brosh RM Jr, Mergny JL. Mendoza O, et al. Nucleic Acids Res. 2016 Mar 18;44(5):1989-2006. doi: 10.1093/nar/gkw079. Epub 2016 Feb 15. Nucleic Acids Res. 2016. PMID: 26883636 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, D1, D2, …
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 …
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 …
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. ...We have attempted to reconcile and integrate numerous observations into a model …
The Fanconi anemia (FA) molecular network consists of 15 "FANC" proteins, of which 13 are associated with mutations in patient …
The Fanconi anemia protein interaction network: casting a wide net.
Rego MA, Kolling FW 4th, Howlett NG. Rego MA, et al. Mutat Res. 2009 Jul 31;668(1-2):27-41. doi: 10.1016/j.mrfmmm.2008.11.018. Epub 2008 Dec 3. Mutat Res. 2009. PMID: 19101576 Free PMC article. Review.
Fornace, Jr., J.B. Little, R.R. Weichselbaum, DNA repair in a Fanconi's anemia fibroblast cell strain, Biochim. Biophys. Acta 561 (1979) 99-109; Y. ...Tatsumi, Repair of mitomycin C damage to DNA in mammalian cells and its impairment in Fanconi's anemia …
Fornace, Jr., J.B. Little, R.R. Weichselbaum, DNA repair in a Fanconi's anemia fibroblast cell strain, Biochim. Biophys. Acta …
The causes of Fanconi anemia in South Asia and the Middle East: A case series and review of the literature.
Thompson AS, Saba N, McReynolds LJ, Munir S, Ahmed P, Sajjad S, Jones K, Yeager M, Donovan FX, Chandrasekharappa SC, Alter BP, Savage SA, Rehman S. Thompson AS, et al. Mol Genet Genomic Med. 2021 Jul;9(7):e1693. doi: 10.1002/mgg3.1693. Epub 2021 May 7. Mol Genet Genomic Med. 2021. PMID: 33960719 Free PMC article. Review.
BACKGROUND: Fanconi anemia (FA) is an inherited bone marrow failure syndrome associated with characteristic dysmorphology primarily caused by biallelic pathogenic germline variants in any of 22 different DNA repair genes. ...
BACKGROUND: Fanconi anemia (FA) is an inherited bone marrow failure syndrome associated with characteristic dysmorphology prim …
FANCM-FAAP24 and FANCJ: FA proteins that metabolize DNA.
Ali AM, Singh TR, Meetei AR. Ali AM, et al. Mutat Res. 2009 Jul 31;668(1-2):20-6. doi: 10.1016/j.mrfmmm.2009.04.002. Epub 2009 Apr 18. Mutat Res. 2009. PMID: 19379763 Free PMC article. Review.
Fanconi anemia (FA) is a rare autosomal recessive or X-linked disorder characterized by aplastic anemia, cancer susceptibility and cellular sensitivity to DNA-crosslinking agents. Eight FA proteins (FANCA, -B, -C, -E, -F, -G, -L and -M) and three non-F …
Fanconi anemia (FA) is a rare autosomal recessive or X-linked disorder characterized by aplastic anemia, cancer suscept …
Molecular pathogenesis of fanconi anemia.
Taniguchi T, Dandrea AD. Taniguchi T, et al. Int J Hematol. 2002 Feb;75(2):123-8. doi: 10.1007/BF02982016. Int J Hematol. 2002. PMID: 11939257 Review.
Fanconi anemia (FA) is a rare autosomal recessive chromosomal breakage disorder characterized by the childhood onset of aplastic anemia, developmental defects, cancer susceptibility, and cellular hypersensitivity to DNA-cross-linking agents. FA patients can b …
Fanconi anemia (FA) is a rare autosomal recessive chromosomal breakage disorder characterized by the childhood onset of aplast …
Molecular pathogenesis of Fanconi anemia.
Collins N, Kupfer GM. Collins N, et al. Int J Hematol. 2005 Oct;82(3):176-83. doi: 10.1532/IJH97.05108. Int J Hematol. 2005. PMID: 16207587 Review.
Fanconi anemia (FA) is a rare inherited disorder characterized clinically by aplastic anemia, developmental defects, and a susceptibility to cancer. Eleven complementation groups have been identified (FA-A, -B, -C, -D1, -D2, -E, -F, -G, -I, -J, …
Fanconi anemia (FA) is a rare inherited disorder characterized clinically by aplastic anemia, developmental defects, an …
20 results