Article
A requirement of FancL and FancD2 monoubiquitination in DNA repair.
Genes to cells : devoted to molecular & cellular mechanisms - 1 Mar 2007
Seki Sohsuke, Ohzeki Mioko, Uchida Akiko, Hirano Seiki, Matsushita Nobuko, Kitao Hiroyuki, Oda Tsukasa, Yamashita Takayuki, Kashihara Naoki, Tsubahara Akio, Takata Minoru, Ishiai Masamichi
Abstract excerpt
The rare hereditary disorder Fanconi anemia (FA) can be caused by mutations in components of the FA core complex (FancA/B/C/E/F/G/L/M), a key regulator FancD2, the breast cancer susceptibility protein BRCA2/FancD1, or the newly identified FancJ/BRIP1 helicase. By performing yeast two-hybrid (Y2H)...
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