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

Visualization and quantification of rDNA instabilities in mammalian cells and mouse models.

哺乳动物细胞和鼠模型中rDNA不稳定性可视化和定量分析。

Zhu Xiaolu, Jiang Wenxia, Wu Wei, Lee Brian J, Menolfi Demis, Tubbs Anthony, Cupo Olivia M, Malkovskiy Eli, Nester Mattie, Wang Xiaobin S, Sims Peter A, Lin Chyuan-Sheng V, Symington Lorraine, Nussenzweig Andre, McStay Brian, Zha Shan

Recurrent patterns of widespread neuronal genomic damage shared by major neurodegenerative disorders.

主要神经退行性疾病共有的广泛神经元基因组损伤的反复出现模式。

Zhou Zinan, Luquette Lovelace J, Dong Guanlan, Kim Junho, Ku Jayoung, Kim Kisong, Bae Mingyun, Shao Diane D, Sahile Bezawit, Miller Michael B, Huang August Yue, Nathan William J, Nussenzweig Andre, Park Peter J, Lagier-Tourenne Clotilde, Lee Eunjung Alice, Walsh Christopher A

A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus.

常见的侧翼变异与 FGF14-SCA27B 重复基因座的稳定性增强有关

Pellerin David, Del Gobbo Giulia F, Couse Madeline, Dolzhenko Egor, Nageshwaran Sathiji K, Cheung Warren A, Xu Isaac R L, Dicaire Marie-Josée, Spurdens Guinevere, Matos-Rodrigues Gabriel, Stevanovski Igor, Scriba Carolin K, Rebelo Adriana, Roth Virginie, Wandzel Marion, Bonnet Céline, Ashton Catherine, Agarwal Aman, Peter Cyril, Hasson Dan, Tsankova Nadejda M, Dewar Ken, Lamont Phillipa J, Laing Nigel G, Renaud Mathilde, Houlden Henry, Synofzik Matthis, Usdin Karen, Nussenzweig Andre, Napierala Marek, Chen Zhao, Jiang Hong, Deveson Ira W, Ravenscroft Gianina, Akbarian Schahram, Eberle Michael A, Boycott Kym M, Pastinen Tomi, Brais Bernard, Zuchner Stephan, Danzi Matt C

Assessment of the Clinical Interactions of GAA Repeat Expansions in FGF14 and FXN.

评估 FGF14 和 FXN 中 GAA 重复扩增的临床相互作用

Gerhart Brandon J, Pellerin David, Danzi Matt C, Zuchner Stephan, Brais Bernard, Matos-Rodrigues Gabriel, Nussenzweig Andre, Usdin Karen, Park Courtney C, Napierala Jill S, Lynch David R, Napierala Marek

The mission to ensure continued funding for excellent basic research

确保为优秀的基础研究提供持续资金的使命

Lamond, Angus I; Dikic, Ivan; Nussenzweig, Andre; Müller, Christoph W; Thornton, Janet M; Yaffe, Michael B

Rapid and precise genotyping of transgene zygosity in mice using an allele-specific method

利用等位基因特异性方法对小鼠转基因合子性进行快速、精确的基因分型

Yang, Jianqi; DeVore, Alison N; Fu, Daniel A; Spicer, Mackenzie M; Guo, Mengcheng; Thompson, Samantha G; Ahlers-Dannen, Katelin E; Polato, Federica; Nussenzweig, Andre; Fisher, Rory A

A genetic roadmap to the response to genotoxic agents in human cells

人类细胞对基因毒性物质反应的遗传路线图

Ciccia, Alberto; Greenberg, Roger A; Lees-Miller, Susan P; Nussenzweig, Andre

The hSSB1 orthologue Obfc2b is essential for skeletogenesis but dispensable for the DNA damage response in vivo

hSSB1 同源物 Obfc2b 对骨骼形成至关重要,但对体内 DNA 损伤反应并非必需。

Feldhahn, Niklas; Ferretti, Elisabetta; Robbiani, Davide F; Callen, Elsa; Deroubaix, Stephanie; Selleri, Licia; Nussenzweig, Andre; Nussenzweig, Michel C

Loss of H3K36 Methyltransferase SETD2 Impairs V(D)J Recombination during Lymphoid Development

H3K36甲基转移酶SETD2的缺失会损害淋巴细胞发育过程中的V(D)J重组。

Chu, S Haihua; Chabon, Jonathan R; Matovina, Chloe N; Minehart, Janna C; Chen, Bo-Ruei; Zhang, Jian; Kumar, Vipul; Xiong, Yijun; Callen, Elsa; Hung, Putzer J; Feng, Zhaohui; Koche, Richard P; Liu, X Shirley; Chaudhuri, Jayanta; Nussenzweig, Andre; Sleckman, Barry P; Armstrong, Scott A

Retraction Notice to: FMN2 Makes Perinuclear Actin to Protect Nuclei during Confined Migration and Promote Metastasis

撤稿声明:FMN2 产生核周肌动蛋白以在受限迁移过程中保护细胞核并促进转移

Skau, Colleen T; Fischer, Robert S; Gurel, Pinar; Thiam, Hawa Racine; Tubbs, Anthony; Baird, Michelle A; Davidson, Michael W; Piel, Matthieu; Alushin, Gregory M; Nussenzweig, Andre; Steeg, Patricia S; Waterman, Clare M