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Molecular Biology Reports|August 24, 2023
Effects of the major formaldehyde catalyzer ADH5 on phenotypes of fanconi anemia zebrafish modelAnfeng Mu, Zimu Cao, Denggao Huang, et al.
Nature Structural & Molecular Biology|November 15, 2011
Formaldehyde catabolism is essential in cells deficient for the Fanconi anemia DNA-repair pathwayIvan V Rosado, Frédéric Langevin, Gerry P Crossan, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 7, 2012
Defining the molecular interface that connects the Fanconi anemia protein FANCM to the Bloom syndrome dissolvasomeKelly A Hoadley, Yutong Xue, Chen Ling, et al.
Journal of Radiation Research|February 21, 2008
Current topics in DNA double-strand break repairJunya Kobayashi, Kuniyoshi Iwabuchi, Kiyoshi Miyagawa, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 2018
Warsaw breakage syndrome DDX11 helicase acts jointly with RAD17 in the repair of bulky lesions and replication through abasic sitesTakuya Abe, Masato Ooka, Ryotaro Kawasumi, et al.
Plos One|September 14, 2011
Direct inhibition of TNF-α promoter activity by Fanconi anemia protein FANCD2Nobuko Matsushita, Yujiro Endo, Koichi Sato, et al.
Cancer Science|February 14, 2007
Characterization of the short isoform of Helios overexpressed in patients with T-cell malignanciesTakayuki Tabayashi, Fumihiko Ishimaru, Minoru Takata, et al.
Journal of the National Cancer Institute|September 16, 2009
Polyclonality of BRAF mutations in acquired melanocytic neviJingrong Lin, Minoru Takata, Hiroshi Murata, et al.
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