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Fanconi Anemia FANCG Protein in Mitigating Radiation- and Enzyme-Induced DNA Double-Strand Breaks by Homologous Recombination in Vertebrate Cells

The rare hereditary disorder Fanconi anemia (FA) is characterized by progressive bone marrow failure, congenital skeletal abnormality, elevated susceptibility to cancer, and cellular hypersensitivity to DNA cross-linking chemicals and sometimes other DNA-damaging agents. Molecular cloning identified...

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Библиографические подробности
Главные авторы: Yamamoto, Kazuhiko, Ishiai, Masamichi, Matsushita, Nobuko, Arakawa, Hiroshi, Lamerdin, Jane E., Buerstedde, Jean-Marie, Tanimoto, Mitsune, Harada, Mine, Thompson, Larry H., Takata, Minoru
Формат: Artigo
Язык:Inglês
Опубликовано: American Society for Microbiology 2003
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Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC165738/
https://ncbi.nlm.nih.gov/pubmed/12861027
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.23.15.5421-5430.2003
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