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| Bibliography | Contents |
|---|---|
| Fanconi anemia and Aldehyde Degradation Deficiency Syndrome: Metabolism and DNA repair protect the genome and hematopoiesis from endogenous DNA damage Mu, Anfeng; Hira, Asuka; Mori, Minako; Okamoto, Yusuke; Takata, Minoru (2023-10) DNA Repair, 130 |  |
| Lack of impact of the ALDH2 rs671 variant on breast cancer development in Japanese BRCA1/2‐mutation carriers Mori, Tomoharu; Okamoto, Yusuke; Mu, Anfeng; Ide, Yoshimi; Yoshimura, Akiyo; Senda, Noriko; Inagaki‐Kawata, Yukiko; Kawashima, Masahiro; Kitao, Hiroyuki; Tokunaga, Eriko; Miyoshi, Yasuo; Ohsumi, Shozo; Tsugawa, Koichiro; Ohta, Tomohiko; Katagiri, Toyomasa; Ohtsuru, Shigeru; Koike, Kaoru; Ogawa, Seishi; Toi, Masakazu; Iwata, Hiroji; Nakamura, Seigo; Matsuo, Keitaro; Takata, Minoru (2023-03) Cancer Medicine, 12(6): 6594-6602 | |
| Effects of the major formaldehyde catalyzer ADH5 on phenotypes of fanconi anemia zebrafish model Mu, Anfeng; Cao, Zimu; Huang, Denggao; Hosokawa, Hiroshi; Maegawa, Shingo; Takata, Minoru (2023-10) Molecular Biology Reports, 50(10): 8385-8395 | |
| Aldehyde degradation deficiency（ADD）症候群 --アルデヒド代謝酵素欠損によるファンコニ貧血症類似の新たな遺伝性骨髄不全症候群の発見-- 牟, 安峰; 平, 明日香; 松尾, 恵太郎; 髙田, 穣 (2021) 臨床血液, 62(6): 547-553 | |
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