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Heme oxygenase-1 and anti-inflammatory M2 macrophages.
Naito Y, Takagi T, Higashimura Y. Naito Y, et al. Arch Biochem Biophys. 2014 Dec 15;564:83-8. doi: 10.1016/j.abb.2014.09.005. Epub 2014 Sep 18. Arch Biochem Biophys. 2014. PMID: 25241054 Review.
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 …
The Fanconi anemia pathway of genomic maintenance.
Levitus M, Joenje H, de Winter JP. Levitus M, et al. Cell Oncol. 2006;28(1-2):3-29. doi: 10.1155/2006/974975. Cell Oncol. 2006. PMID: 16675878 Free PMC article. Review.
Fanconi anemia (FA), a recessive syndrome with both autosomal and X-linked inheritance, features diverse clinical symptoms, such as progressive bone marrow failure, hypersensitivity to DNA cross-linking agents, chromosomal instability and susceptibility to cancer. A …
Fanconi anemia (FA), a recessive syndrome with both autosomal and X-linked inheritance, features diverse clinical symptoms, su …
Beyond interstrand crosslinks repair: contribution of FANCD2 and other Fanconi Anemia proteins to the replication of DNA.
Federico MB, Campodónico P, Paviolo NS, Gottifredi V. Federico MB, et al. Mutat Res. 2018 Mar;808:83-92. doi: 10.1016/j.mrfmmm.2017.09.004. Epub 2017 Sep 14. Mutat Res. 2018. PMID: 29031493 Review.
Biallelic mutations of FANCD2 and other components of the Fanconi Anemia (FA) pathway cause a disease characterized by bone marrow failure, cancer predisposition and a striking sensitivity to agents that induce crosslinks between the two complementary DNA strands (i …
Biallelic mutations of FANCD2 and other components of the Fanconi Anemia (FA) pathway cause a disease characterized by bone ma …
Emerging roles for centromere-associated proteins in DNA repair and genetic recombination.
Osman F, Whitby MC. Osman F, et al. Biochem Soc Trans. 2013 Dec;41(6):1726-30. doi: 10.1042/BST20130200. Biochem Soc Trans. 2013. PMID: 24256282 Review.
Centromere proteins CENP-S and CENP-X are members of the constitutive centromere-associated network, which is a conserved group of proteins that are needed for the assembly and function of kinetochores at centromeres. ...In this guise they function with a DNA translocase c …
Centromere proteins CENP-S and CENP-X are members of the constitutive centromere-associated network, which is a conserved group of pr …
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. Fujiwara, M. Tatsumi, Repair of mitomycin C damage to DNA in mammalian cells and its impairment in Fanconi …
Fornace, Jr., J.B. Little, R.R. Weichselbaum, DNA repair in a Fanconi's anemia fibroblast cell strain, Biochim. Biophys. Acta …
Learning from a paradox: recent insights into Fanconi anaemia through studying mouse models.
Bakker ST, de Winter JP, te Riele H. Bakker ST, et al. Dis Model Mech. 2013 Jan;6(1):40-7. doi: 10.1242/dmm.009795. Dis Model Mech. 2013. PMID: 23268537 Free PMC article. Review.
Fanconi anaemia (FA) is a rare autosomal recessive or X-linked inherited disease characterised by an increased incidence of bone marrow failure (BMF), haematological malignancies and solid tumours. Cells from individuals with FA show a pronounced sensitivity to DNA interst …
Fanconi anaemia (FA) is a rare autosomal recessive or X-linked inherited disease characterised by an increased incidence of bone marr …
Fanconi anaemia proteins: major roles in cell protection against oxidative damage.
Pagano G, Youssoufian H. Pagano G, et al. Bioessays. 2003 Jun;25(6):589-95. doi: 10.1002/bies.10283. Bioessays. 2003. PMID: 12766948 Review.
Fanconi anaemia (FA) is a cancer-prone genetic disorder that is characterised by cytogenetic instability and redox abnormalities. ...
Fanconi anaemia (FA) is a cancer-prone genetic disorder that is characterised by cytogenetic instability and redox abnormalities. ...