Recent Publications on Fanconi Anemia Complementation Group L Protein: |  |
| [Functions of FANCL in primordial germ cell formation and Fanconi anemia]
| 19th August, 2008
| Beijing Institute of Biotechnology, Beijing 100071, China.
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UBE2T, the Fanconi anemia core complex, and FANCD2 are recruited independently to chromatin: a basis for the regulation of FANCD2 monoubiquitination.
The Fanconi anemia (FA) nuclear core complex and the E2...
Direct Link | 19th December, 2007
| Laboratory of Molecular Biology, Medical Research Council, Cambridge,
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FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway.
The Fanconi anemia (FA) core complex plays a central role in the DNA...
Direct Link | 5th October, 2007
| Laboratory of Genetics, National Institute on Aging, National Institutes
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| Altered expression of FANCL confers mitomycin C sensitivity in Calu-6 lung cancer cells.
| 26th May, 2007
| Department of Laboratory Medicine and Pathology, Mayo Clinic College of
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A requirement of FancL and FancD2 monoubiquitination in DNA repair.
The rare hereditary disorder Fanconi anemia (FA) can be caused by...
Direct Link | 4th May, 2007
| Department of Immunology and Molecular Genetics, Kawasaki Medical School,
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Drosophila homologs of FANCD2 and FANCL function in DNA repair.
Fanconi anemia (FA) is a genetically heterogeneous disease characterized...
Direct Link | 6th January, 2007
| Department of Genetics, Yale University School of Medicine, 333 Cedar St.,
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Evidence for subcomplexes in the Fanconi anemia pathway.
Fanconi anemia (FA) is a genomic instability disorder, clinically...
Direct Link | 17th October, 2006
| Department of Clinical Genetics and Human Genetics, Vrije Universiteit
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UBE2T is the E2 in the Fanconi anemia pathway and undergoes negative autoregulation.
The Fanconi anemia pathway is required for the efficient repair of damaged...
Direct Link | 20th September, 2006
| Department of Biochemistry and Molecular Genetics, University of Virginia
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The WD40 repeats of FANCL are required for Fanconi anemia core complex assembly.
Fanconi anemia (FA) is an autosomal recessive disorder characterized by...
Direct Link | 14th June, 2006
| Biological and Biomedical Sciences Program, Dana-Farber Cancer Institute,
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Inducibility of nuclear Rad51 foci after DNA damage distinguishes all Fanconi anemia complementation groups from D1/BRCA2.
Fanconi anemia (FA) is a cancer susceptibility disorder characterized by...
Direct Link | 29th March, 2006
| Department of Toxicogenetics, Leiden University Medical Center,
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Germ-cell specific protein gametogenetin protein 2 (GGN2), expression in the testis, and association with intracellular membrane.
Gametogenetin (Ggn) is a germ cell-specific gene with multiple splicing...
Direct Link | 3rd November, 2005
| Beijing Institute of Biotechnology, Beijing, China.
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A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.
Fanconi anemia is a genetic disease characterized by genomic instability...
Direct Link | 30th September, 2005
| Division of Experimental Hematology, Cincinnati Children's Hospital
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| FANCL replaces BRCA1 as the likely ubiquitin ligase responsible for FANCD2 monoubiquitination.
| 22nd May, 2004
| Laboratory of Genetics, National Institute on Aging, National Institutes
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A novel ubiquitin ligase is deficient in Fanconi anemia.
Fanconi anemia is a recessively inherited disease characterized by...
Direct Link | 9th December, 2003
| Laboratory of Genetics, National Institute on Aging, National Institutes
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