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

A non-syndromic orofacial cleft risk locus links tRNA splicing defects to neural crest cell pathologies.

非综合征性口面裂风险基因位点将 tRNA 剪接缺陷与神经嵴细胞病变联系起来

Bartusel Michaela, Kim Skylar X, Rehimi Rizwan, Darnell Alicia M, Nikolić Miloš, Heggemann Julia, Kolovos Petros, van Ijcken Wilfred F J, Varineau Jade, Crispatzu Giuliano, Mangold Elisabeth, Brugmann Samantha A, Vander Heiden Matthew G, Laugsch Magdalena, Ludwig Kerstin U, Rada-Iglesias Alvaro, Calo Eliezer

Remodeling of the endothelial cell transcriptional program via paracrine and DNA-binding activities of MPO

通过 MPO 的旁分泌和 DNA 结合活性重塑内皮细胞转录程序

Ruiyuan Zheng, Kyle Moynahan, Theodoros Georgomanolis, Egor Pavlenko, Simon Geissen, Athanasia Mizi, Simon Grimm, Harshal Nemade, Rizwan Rehimi, Jil Bastigkeit, Jan-Wilm Lackmann, Matti Adam, Alvaro Rada-Iglesias, Peter Nuernberg, Anna Klinke, Simon Poepsel, Stephan Baldus, Argyris Papantonis, Yulia

Overarching control of autophagy and DNA damage response by CHD6 revealed by modeling a rare human pathology

通过模拟罕见人类病理揭示 CHD6 对自噬和 DNA 损伤反应的总体控制

Yulia Kargapolova, Rizwan Rehimi, Hülya Kayserili, Joanna Brühl, Konstantinos Sofiadis, Anne Zirkel, Spiros Palikyras, Athanasia Mizi, Yun Li, Gökhan Yigit, Alexander Hoischen, Stefan Frank, Nicole Russ, Jonathan Trautwein, Bregje van Bon, Christian Gilissen, Magdalena Laugsch, Eduardo Gade Gusmao, 

The chromatin, topological and regulatory properties of pluripotency-associated poised enhancers are conserved in vivo

多能性相关平衡增强子的染色质、拓扑和调控特性在体内得到保留

Giuliano Crispatzu #, Rizwan Rehimi #, Tomas Pachano, Tore Bleckwehl, Sara Cruz-Molina, Cally Xiao, Esther Mahabir, Hisham Bazzi, Alvaro Rada-Iglesias

MAPRE2 mutations result in altered human cranial neural crest migration, underlying craniofacial malformations in CSC-KT syndrome

MAPRE2 突变导致人类颅神经嵴移位发生改变,从而导致 CSC-KT 综合征的颅面畸形

Cedric Thues, Jorge S Valadas, Liesbeth Deaulmerie, Ann Geens, Amit K Chouhan, Ramon Duran-Romaña, Joost Schymkowitz, Frederic Rousseau, Michaela Bartusel, Rizwan Rehimi, Alvaro Rada-Iglesias, Patrik Verstreken, Hilde Van Esch0

yylncT Defines a Class of Divergently Transcribed lncRNAs and Safeguards the T-mediated Mesodermal Commitment of Human PSCs

yylncT 定义了一类不同转录的 lncRNA,并保障了 T 介导的人类 PSC 的中胚层定位

Stefan Frank, Gaurav Ahuja, Deniz Bartsch, Nicole Russ, Wenjie Yao, Joseph Chao-Chung Kuo, Jens-Peter Derks, Vijay Suresh Akhade, Yulia Kargapolova, Theodore Georgomanolis, Jan-Erik Messling, Marie Gramm, Lilija Brant, Rizwan Rehimi, Natalia Emilse Vargas, Alina Kuroczik, Tsun-Po Yang, Raja Ghazanfa

Modeling the Pathological Long-Range Regulatory Effects of Human Structural Variation with Patient-Specific hiPSCs

利用患者特异性 hiPSC 模拟人类结构变异的病理性长程调节效应

Magdalena Laugsch, Michaela Bartusel, Rizwan Rehimi, Hafiza Alirzayeva, Agathi Karaolidou, Giuliano Crispatzu, Peter Zentis, Milos Nikolic, Tore Bleckwehl, Petros Kolovos, Wilfred F J van Ijcken, Tomo Šarić, Katrin Koehler, Peter Frommolt, Katherine Lachlan, Julia Baptista, Alvaro Rada-Iglesias

Pathological ASXL1 Mutations and Protein Variants Impair Neural Crest Development

病理性ASXL1突变和蛋白质变异会损害神经嵴发育

Matheus, Friederike; Rusha, Ejona; Rehimi, Rizwan; Molitor, Lena; Pertek, Anna; Modic, Miha; Feederle, Regina; Flatley, Andrew; Kremmer, Elisabeth; Geerlof, Arie; Rishko, Valentyna; Rada-Iglesias, Alvaro; Drukker, Micha

Chromatin Immunoprecipitation (ChIP) Protocol for Low-abundance Embryonic Samples

低丰度胚胎样本的染色质免疫沉淀(ChIP)方案

Rehimi, Rizwan; Bartusel, Michaela; Solinas, Francesca; Altmüller, Janine; Rada-Iglesias, Alvaro