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

A Cellular and Transcriptomic Atlas of the Aged Mouse Hematopoietic System

老年小鼠造血系统的细胞和转录组图谱

White, Ryan R; Xiong, Kun; Wakai, Matthew; Surian, Allison; Adler, Christina; Negron, Nicole; Ni, Min; Shavlakadze, Tea; Bai, Yu; Glass, David J

ALDH9A1 deficiency as a source of endogenous DNA damage that requires repair by the Fanconi anemia pathway.

ALDH9A1 缺乏是内源性 DNA 损伤的来源,需要通过范可尼贫血途径进行修复

Jung Moonjung, Kim Jungwoo, Park Yeji, Ilyashov Isaac, Yang Fan, Choijilsuren Haruna B, Keahi Danielle, Durmaz Jordan A, Bea Habin, Goldfarb Audrey M, Stein Mia D, Wong Claudia, White Ryan R, Sridhar Sunandini, Noonan Raymond, Wiley Tom F, Carroll Thomas S, Lach Francis P, Jeong Sangmoo, Miranda Ileana C, Smogorzewska Agata

Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes

作者更正:常见和罕见变异与克隆性造血表型的关联

Kessler, Michael D; Damask, Amy; O'Keeffe, Sean; Banerjee, Nilanjana; Li, Dadong; Watanabe, Kyoko; Marketta, Anthony; Van Meter, Michael; Semrau, Stefan; Horowitz, Julie; Tang, Jing; Kosmicki, Jack A; Rajagopal, Veera M; Zou, Yuxin; Houvras, Yariv; Ghosh, Arkopravo; Gillies, Christopher; Mbatchou, Joelle; White, Ryan R; Verweij, Niek; Bovijn, Jonas; Parikshak, Neelroop N; LeBlanc, Michelle G; Jones, Marcus; Glass, David J; Lotta, Luca A; Cantor, Michael N; Atwal, Gurinder S; Locke, Adam E; Ferreira, Manuel A R; Deering, Raquel; Paulding, Charles; Shuldiner, Alan R; Thurston, Gavin; Ferrando, Adolfo A; Salerno, Will; Reid, Jeffrey G; Overton, John D; Marchini, Jonathan; Kang, Hyun M; Baras, Aris; Abecasis, Gonçalo R; Jorgenson, Eric

Common and rare variant associations with clonal haematopoiesis phenotypes

常见和罕见变异与克隆性造血表型的关联

Kessler, Michael D; Damask, Amy; O'Keeffe, Sean; Banerjee, Nilanjana; Li, Dadong; Watanabe, Kyoko; Marketta, Anthony; Van Meter, Michael; Semrau, Stefan; Horowitz, Julie; Tang, Jing; Kosmicki, Jack A; Rajagopal, Veera M; Zou, Yuxin; Houvras, Yariv; Ghosh, Arkopravo; Gillies, Christopher; Mbatchou, Joelle; White, Ryan R; Verweij, Niek; Bovijn, Jonas; Parikshak, Neelroop N; LeBlanc, Michelle G; Jones, Marcus; Glass, David J; Lotta, Luca A; Cantor, Michael N; Atwal, Gurinder S; Locke, Adam E; Ferreira, Manuel A R; Deering, Raquel; Paulding, Charles; Shuldiner, Alan R; Thurston, Gavin; Ferrando, Adolfo A; Salerno, Will; Reid, Jeffrey G; Overton, John D; Marchini, Jonathan; Kang, Hyun M; Baras, Aris; Abecasis, Gonçalo R; Jorgenson, Eric

FOXO3a acts to suppress DNA double-strand break-induced mutations

FOXO3a 可抑制 DNA 双链断裂诱导的突变

White, Ryan R; Maslov, Alexander Y; Lee, Moonsook; Wilner, Samantha E; Levy, Matthew; Vijg, Jan

Inducible aging in Hydra oligactis implicates sexual reproduction, loss of stem cells, and genome maintenance as major pathways

水螅的诱导衰老表明,有性生殖、干细胞丢失和基因组维持是主要途径。

Sun, Shixiang; White, Ryan R; Fischer, Kathleen E; Zhang, Zhengdong; Austad, Steven N; Vijg, Jan

Controlled induction of DNA double-strand breaks in the mouse liver induces features of tissue ageing

在小鼠肝脏中控制性诱导DNA双链断裂可诱发组织衰老特征

White, Ryan R; Milholland, Brandon; de Bruin, Alain; Curran, Samuel; Laberge, Remi-Martin; van Steeg, Harry; Campisi, Judith; Maslov, Alexander Y; Vijg, Jan

DNA repair in species with extreme lifespan differences

寿命差异极大的物种的DNA修复

MacRae, Sheila L; Croken, Matthew McKnight; Calder, R B; Aliper, Alexander; Milholland, Brandon; White, Ryan R; Zhavoronkov, Alexander; Gladyshev, Vadim N; Seluanov, Andrei; Gorbunova, Vera; Zhang, Zhengdong D; Vijg, Jan

High-throughput sequencing in mutation detection: A new generation of genotoxicity tests?

高通量测序在突变检测中的应用:新一代基因毒性测试?

Maslov, Alexander Y; Quispe-Tintaya, Wilber; Gorbacheva, Tatyana; White, Ryan R; Vijg, Jan