日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Mouse Slfn8 and Slfn9 genes complement human cells lacking SLFN11 during the replication stress response

在复制应激反应期间,小鼠 Slfn8 和 Slfn9 基因可以补偿缺乏 SLFN11 的人类细胞。

Alvi, Erin; Mochizuki, Ayako L; Katsuki, Yoko; Ogawa, Minori; Qi, Fei; Okamoto, Yusuke; Takata, Minoru; Mu, Anfeng

Lack of impact of the ALDH2 rs671 variant on breast cancer development in Japanese BRCA1/2-mutation carriers

ALDH2 rs671变异对日本BRCA1/2突变携带者乳腺癌发展无影响

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

Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients

通过多模态方法在117名日本范可尼贫血患者中鉴定出致病突变

Mori, Minako; Hira, Asuka; Yoshida, Kenichi; Muramatsu, Hideki; Okuno, Yusuke; Shiraishi, Yuichi; Anmae, Michiko; Yasuda, Jun; Tadaka, Shu; Kinoshita, Kengo; Osumi, Tomoo; Noguchi, Yasushi; Adachi, Souichi; Kobayashi, Ryoji; Kawabata, Hiroshi; Imai, Kohsuke; Morio, Tomohiro; Tamura, Kazuo; Takaori-Kondo, Akifumi; Yamamoto, Masayuki; Miyano, Satoru; Kojima, Seiji; Ito, Etsuro; Ogawa, Seishi; Matsuo, Keitaro; Yabe, Hiromasa; Yabe, Miharu; Takata, Minoru

USP42 enhances homologous recombination repair by promoting R-loop resolution with a DNA-RNA helicase DHX9

USP42 通过促进 DNA-RNA 解旋酶 DHX9 的 R 环解离来增强同源重组修复。

Matsui, Misaki; Sakasai, Ryo; Abe, Masako; Kimura, Yusuke; Kajita, Shoki; Torii, Wakana; Katsuki, Yoko; Ishiai, Masamichi; Iwabuchi, Kuniyoshi; Takata, Minoru; Nishi, Ryotaro

Significance of 5-S-Cysteinyldopa as a Marker for Melanoma

5-S-半胱氨酰多巴作为黑色素瘤标志物的意义

Wakamatsu, Kazumasa; Fukushima, Satoshi; Minagawa, Akane; Omodaka, Toshikazu; Hida, Tokimasa; Hatta, Naohito; Takata, Minoru; Uhara, Hisashi; Okuyama, Ryuhei; Ihn, Hironobu

A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India

南亚人群中的一种创始人变异导致印度范可尼贫血症(FANCL)病例高发。

Donovan, Frank X; Solanki, Avani; Mori, Minako; Chavan, Niranjan; George, Merin; C, Selvaa Kumar; Okuno, Yusuke; Muramastsu, Hideki; Yoshida, Kenichi; Shimamoto, Akira; Takaori-Kondo, Akifumi; Yabe, Hiromasa; Ogawa, Seishi; Kojima, Seiji; Yabe, Miharu; Ramanagoudr-Bhojappa, Ramanagouda; Smogorzewska, Agata; Mohan, Sheila; Rajendran, Aruna; Auerbach, Arleen D; Takata, Minoru; Chandrasekharappa, Settara C; Vundinti, Babu Rao

Participation of TDP1 in the repair of formaldehyde-induced DNA-protein cross-links in chicken DT40 cells

TDP1参与修复鸡DT40细胞中甲醛诱导的DNA-蛋白质交联

Nakano, Toshiaki; Shoulkamy, Mahmoud I; Tsuda, Masataka; Sasanuma, Hiroyuki; Hirota, Kouji; Takata, Minoru; Masunaga, Shin-Ichiro; Takeda, Shunichi; Ide, Hiroshi; Bessho, Tadayoshi; Tano, Keizo

Novel quantitative trait loci for low grain cadmium concentration in common wheat (Triticum aestivum L.)

普通小麦(Triticum aestivum L.)籽粒低镉浓度的新型数量性状基因座

Yusuke Ban, Goro Ishikawa, Hiroaki Ueda, Naoyuki Ishikawa, Keita Kato, Kanenori Takata, Minoru Matsuyama, Hirokazu Handa, Toshiki Nakamura, Mikiko Yanaka

Warsaw breakage syndrome DDX11 helicase acts jointly with RAD17 in the repair of bulky lesions and replication through abasic sites

华沙断裂综合征中的DDX11解旋酶与RAD17协同作用,修复大块损伤并通过无碱基位点进行复制。

Abe, Takuya; Ooka, Masato; Kawasumi, Ryotaro; Miyata, Keiji; Takata, Minoru; Hirota, Kouji; Branzei, Dana

Pluripotent cell models of fanconi anemia identify the early pathological defect in human hemoangiogenic progenitors

范可尼贫血的多能干细胞模型揭示了人类血管生成祖细胞的早期病理缺陷

Suzuki, Naoya M; Niwa, Akira; Yabe, Miharu; Hira, Asuka; Okada, Chihiro; Amano, Naoki; Watanabe, Akira; Watanabe, Ken-Ichiro; Heike, Toshio; Takata, Minoru; Nakahata, Tatsutoshi; Saito, Megumu K