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

PIN1-SUMO2/3 motif suppresses excessive RNF168 chromatin accumulation and ubiquitin signaling to promote IR resistance.

PIN1-SUMO2/3 基序抑制 RNF168 染色质过度积累和泛素信号传导,从而促进 IR 抗性

Chauhan Anoop S, Mackintosh Matthew J W, Cassar Joseph, Lanz Alexander J, Jamshad Mohammed, Mackay Hannah L, Garvin Alexander J, Walker Alexandra K, Jhujh Satpal S, Carlomagno Teresa, Leney Aneika C, Stewart Grant S, Morris Joanna R

Inherited deficiency of DIAPH1 identifies a DNA double strand break repair pathway regulated by γ-actin.

DIAPH1 的遗传性缺陷揭示了由 α-肌动蛋白调控的 DNA 双链断裂修复途径

Woodward Beth L, Lahiri Sudipta, Chauhan Anoop S, Garcia Marcos Rios, Goodley Lucy E, Clarke Thomas L, Pal Mohinder, Agathanggelou Angelo, Jhujh Satpal S, Ganesh Anil N, Hollins Fay M, Deforie Valentina Galassi, Maroofian Reza, Efthymiou Stephanie, Meinhardt Andrea, Mathew Christopher G, Simpson Michael A, Mefford Heather C, Faqeih Eissa A, Rosenzweig Sergio D, Volpi Stefano, Di Matteo Gigliola, Cancrini Caterina, Scardamaglia Annarita, Shackley Fiona, Davies E Graham, Ibrahim Shahnaz, Arkwright Peter D, Zaki Maha S, Stankovic Tatjana, Taylor A Malcolm R, Mazur Antonina J, Di Donato Nataliya, Houlden Henry, Rothenberg Eli, Stewart Grant S

E3 ligases: a ubiquitous link between DNA repair, DNA replication and human disease

E3连接酶:DNA修复、DNA复制和人类疾病之间普遍存在的联系

Chauhan, Anoop S; Jhujh, Satpal S; Stewart, Grant S