Abnormal rearrangements associated with V(D)J recombination in fanconi anemia
- 4 September 1998
- journal article
- Published by Elsevier in Journal of Molecular Biology
- Vol. 281 (5), 815-825
- https://doi.org/10.1006/jmbi.1998.1971
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Fanconi anemia C gene product plays a role in the fidelity of blunt DNA end-joiningJournal of Molecular Biology, 1998
- The fidelity of double strand breaks processing is impaired in complementation groups B and D of Fanconi anemia, a genetic instability syndrome.Somatic Cell and Molecular Genetics, 1997
- Ku70-deficient embryonic stem cells have increased ionizing radiosensitivity, defective DNA end-binding activity, and inability to support V(D)J recombinationProceedings of the National Academy of Sciences, 1997
- RAG1 and RAG2 Form a Stable Postcleavage Synaptic Complex with DNA Containing Signal Ends in V(D)J RecombinationCell, 1997
- A new view of V(D)J recombinationGenes to Cells, 1996
- DNA double-strand break repair and V(D)J recombination: involvement of DNA-PKTrends in Biochemical Sciences, 1995
- V(D)J recombination in ataxia telangiectasia, Bloom's syndrome, and a DNA ligase I-associated immunodeficiency disorder.Published by Elsevier ,1993
- Leukemia and preleukemia in Fanconi anemia patients: A review of the literature and report of the International Fanconi Anemia RegistryCancer Genetics and Cytogenetics, 1991
- International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivityBlood, 1989
- Assay for gene mutation in a human lymphoblast line, AHH-1, competent for xenobiotic metabolismMutation Research, 1984