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Plos One|December 2, 2016
Homologous Recombination and Translesion DNA Synthesis Play Critical Roles on Tolerating DNA Damage Caused by Trace Levels of Hexavalent ChromiumXu Tian, Keyur Patel, John R Ridpath, et al.
British Journal of Haematology|July 6, 2016
The phenotype and clinical course of Japanese Fanconi Anaemia infants is influenced by patient, but not maternal ALDH2 genotypeMiharu Yabe, Hiromasa Yabe, Tsuyoshi Morimoto, et al.
Nucleic Acids Research|October 2, 2007
Subcellular distribution of human RDM1 protein isoforms and their nucleolar accumulation in response to heat shock and proteotoxic stressLydia Messaoudi, Yun-Gui Yang, Aiko Kinomura, et al.
The EMBO Journal|December 24, 2004
Functional relationships of FANCC to homologous recombination, translesion synthesis, and BLMSeiki Hirano, Kazuhiko Yamamoto, Masamichi Ishiai, et al.
Nature|November 8, 2002
Nbs1 is essential for DNA repair by homologous recombination in higher vertebrate cellsHiroshi Tauchi, Junya Kobayashi, Ken-ichi Morishima, et al.
American Journal of Human Genetics|June 6, 2015
Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemiaAsuka Hira, Kenichi Yoshida, Koichi Sato, et al.
Molecular Cell|June 26, 2018
Histone Methylation by SETD1A Protects Nascent DNA through the Nucleosome Chaperone Activity of FANCD2Martin R Higgs, Koichi Sato, John J Reynolds, et al.
Annals of Hematology|October 29, 2018
Associations of complementation group, ALDH2 genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemiaMiharu Yabe, Takashi Koike, Keisuke Ohtsubo, et al.
Cancer Research|December 7, 2007
Cells deficient in the FANC/BRCA pathway are hypersensitive to plasma levels of formaldehydeJohn R Ridpath, Ayumi Nakamura, Keizo Tano, et al.
Blood|January 29, 2021
Analysis of disease model iPSCs derived from patients with a novel Fanconi anemia-like IBMFS ADH5/ALDH2 deficiencyAnfeng Mu, Asuka Hira, Akira Niwa, et al.
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