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

An unexpected role of CLASP1 in radiation response and S-phase regulation of head and neck cancer cells

CLASP1在头颈癌细胞的放射反应和S期调控中发挥意想不到的作用

de Roest, Reinout H; Buijze, Marijke; Veth, Myrthe; de Lint, Klaas; Pai, Govind; Rooimans, Martin A; Wolthuis, Rob M F; Brink, Arjen; Poell, Jos B; Brakenhoff, Ruud H

MMS22L-TONSL functions in sister chromatid cohesion in a pathway parallel to DSCC1-RFC

MMS22L-TONSL 在与 DSCC1-RFC 平行的通路中参与姐妹染色单体黏连。

van Schie, Janne Jm; de Lint, Klaas; Pai, Govind M; Rooimans, Martin A; Wolthuis, Rob Mf; de Lange, Job

Acquired cross-linker resistance associated with a novel spliced BRCA2 protein variant for molecular phenotyping of BRCA2 disruption.

获得性交联剂抗性与一种新型剪接 BRCA2 蛋白变体相关,用于 BRCA2 破坏的分子表型分析

Meyer Stefan, Stevens Adam, Paredes Roberto, Schneider Marion, Walker Michael J, Williamson Andrew J K, Gonzalez-Sanchez Maria-Belen, Smetsers Stephanie, Dalal Vineet, Teng Hsiang Ying, White Daniel J, Taylor Sam, Muter Joanne, Pierce Andrew, de Leonibus Chiara, Rockx Davy A P, Rooimans Martin A, Spooncer Elaine, Stauffer Stacey, Biswas Kajal, Godthelp Barbara, Dorsman Josephine, Clayton Peter E, Sharan Shyam K, Whetton Anthony D

A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51

一种与 RAD51 基因显性负突变相关的新型范可尼贫血亚型

Ameziane, Najim; May, Patrick; Haitjema, Anneke; van de Vrugt, Henri J; van Rossum-Fikkert, Sari E; Ristic, Dejan; Williams, Gareth J; Balk, Jesper; Rockx, Davy; Li, Hong; Rooimans, Martin A; Oostra, Anneke B; Velleuer, Eunike; Dietrich, Ralf; Bleijerveld, Onno B; Maarten Altelaar, A F; Meijers-Heijboer, Hanne; Joenje, Hans; Glusman, Gustavo; Roach, Jared; Hood, Leroy; Galas, David; Wyman, Claire; Balling, Rudi; den Dunnen, Johan; de Winter, Johan P; Kanaar, Roland; Gelinas, Richard; Dorsman, Josephine C

Coregulation of FANCA and BRCA1 in human cells

人类细胞中FANCA和BRCA1的协同调控

Haitjema, Anneke; Mol, Berber M; Kooi, Irsan E; Massink, Maarten Pg; Jørgensen, Jens Al; Rockx, Davy Ap; Rooimans, Martin A; de Winter, Johan P; Meijers-Heijboer, Hanne; Joenje, Hans; Dorsman, Josephine C

Warsaw breakage syndrome, a cohesinopathy associated with mutations in the XPD helicase family member DDX11/ChlR1

华沙断裂综合征是一种与 XPD 解旋酶家族成员 DDX11/ChlR1 基因突变相关的黏连蛋白病。

van der Lelij, Petra; Chrzanowska, Krystyna H; Godthelp, Barbara C; Rooimans, Martin A; Oostra, Anneke B; Stumm, Markus; Zdzienicka, Małgorzata Z; Joenje, Hans; de Winter, Johan P

Identification of the Fanconi anemia complementation group I gene, FANCI

范可尼贫血互补组 I 基因 (FANCI) 的鉴定

Dorsman, Josephine C; Levitus, Marieke; Rockx, Davy; Rooimans, Martin A; Oostra, Anneke B; Haitjema, Anneke; Bakker, Sietske T; Steltenpool, Jûrgen; Schuler, Dezsö; Mohan, Sheila; Schindler, Detlev; Arwert, Fré; Pals, Gerard; Mathew, Christopher G; Waisfisz, Quinten; de Winter, Johan P; Joenje, Hans