Robin van Schendel相关文献与解析，生知库 | 链接生命科学的每一步

日期影响因子

Double-strand breaks in facultative heterochromatin require specific movements and chromatin changes for efficient repair

兼性异染色质的双链断裂需要特定的运动和染色质变化才能有效修复

期刊:Nature Communications

影响因子:14.7

doi:10.1038/s41467-024-53313-2

Marieke R Wensveen, Aditya A Dixit, Robin van Schendel, Apfrida Kendek, Jan-Paul Lambooij, Marcel Tijsterman, Serafin U Colmenares, Aniek Janssen

发表日期：2024

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Dissecting the genetic landscape of GPCR signaling through phenotypic profiling in C. elegans

通过秀丽隐杆线虫的表型分析解析 GPCR 信号的遗传图谱

期刊:Nature Communications

影响因子:14.7

doi:10.1038/s41467-023-44177-z

Longjun Pu #, Jing Wang #, Qiongxuan Lu, Lars Nilsson, Alison Philbrook, Anjali Pandey, Lina Zhao, Robin van Schendel, Alan Koh, Tanara V Peres, Weheliye H Hashi, Si Lhyam Myint, Chloe Williams, Jonathan D Gilthorpe, Sun Nyunt Wai, Andre Brown, Marcel Tijsterman, Piali Sengupta, Johan Henriksson, Ch

GPCR/Calcium/cAMP

发表日期：2023

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CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations

CRISPR-Cas9 在体内靶位点和非靶位点诱导产生大的结构变异，这些变异会跨代遗传。

影响因子:14.7

doi:10.1038/s41467-022-28244-5.

Ida Höijer,Anastasia Emmanouilidou,Rebecka Östlund,Robin van Schendel,Selma Bozorgpana,Marcel Tijsterman,Lars Feuk,Ulf Gyllensten,Marcel den Hoed #,Adam Ameur #

发表日期：2022

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High-resolution breakpoint junction mapping of proximally extended D4Z4 deletions in FSHD1 reveals evidence for a founder effect

对 FSHD1 中近端延伸的 D4Z4 缺失进行高分辨率断点连接定位，揭示了创始人效应的证据。

期刊:Human Molecular Genetics

影响因子:3.1

doi:10.1093/hmg/ddab250.

Richard J L F Lemmers ,Patrick J van der Vliet ,David San Leon Granado ,Nienke van der Stoep ,Henk Buermans ,Robin van Schendel ,Joost Schimmel ,Marianne de Visser ,Rudy van Coster ,Marc Jeanpierre ,Pascal Laforet ,Meena Upadhyaya ,Baziel van Engelen ,Sabrina Sacconi ,Rabi Tawil ,Nicol C Voermans ,Mark Rogers ,Silvère M van der Maarel

发表日期：2022

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Small tandem DNA duplications result from CST-guided Pol α-primase action at DNA break termini

CST 引导的 Pol α-引物酶在 DNA 断裂末端的作用导致小的串联 DNA 重复

期刊:Nature Communications

影响因子:14.7

doi:10.1038/s41467-021-25154-w

Joost Schimmel, Núria Muñoz-Subirana, Hanneke Kool, Robin van Schendel, Marcel Tijsterman

发表日期：2021

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Preservation of lagging strand integrity at sites of stalled replication by Pol α-primase and 9-1-1 complex

Pol α-引物酶和 9-1-1 复合物在复制停滞位点保持滞后链的完整性

期刊:Science Advances

影响因子:11.7

doi:10.1126/sciadv.abf2278

Robin van Schendel, Ron Romeijn, Helena Buijs, Marcel Tijsterman

发表日期：2021

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Mutational signatures of non-homologous and polymerase theta-mediated end-joining in embryonic stem cells

胚胎干细胞中非同源和聚合酶θ介导的末端连接的突变特征

期刊:EMBO Journal

影响因子:9.4

doi:10.15252/embj.201796948

Joost Schimmel, Hanneke Kool, Robin van Schendel, Marcel Tijsterman

发育与干细胞

发表日期：2017

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High density of REC8 constrains sister chromatid axes and prevents illegitimate synaptonemal complex formation

高密度的 REC8 限制了姐妹染色单体轴并阻止了不正常的联会复合体的形成

期刊:EMBO Reports

影响因子:6.5

doi:10.15252/embr.201642030

Ana Agostinho, Otto Manneberg, Robin van Schendel, Abrahan Hernández-Hernández, Anna Kouznetsova, Hans Blom, Hjalmar Brismar, Christer Höög

发表日期：2016

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