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

FOXO1-mediated lipid metabolism maintains mammalian embryos in dormancy

FOXO1 介导的脂质代谢维持哺乳动物胚胎处于休眠状态

Vera A van der Weijden, Maximilian Stötzel, Dhanur P Iyer, Beatrix Fauler, Elzbieta Gralinska, Mohammed Shahraz, David Meierhofer, Martin Vingron, Steffen Rulands, Theodore Alexandrov, Thorsten Mielke, Aydan Bulut-Karslioglu

Dual function of a highly conserved bacteriophage tail completion protein essential for bacteriophage infectivity

高度保守的噬菌体尾部完成蛋白的双重功能对噬菌体感染至关重要

Isabelle Auzat, Malika Ouldali, Eric Jacquet, Beatrix Fauler, Thorsten Mielke, Paulo Tavares

A critical period of translational control during brain development at codon resolution

密码子解析过程中大脑发育过程中翻译控制的关键时期

Dermot Harnett #, Mateusz C Ambrozkiewicz #, Ulrike Zinnall, Alexandra Rusanova, Ekaterina Borisova, Amelie N Drescher, Marta Couce-Iglesias, Gabriel Villamil, Rike Dannenberg, Koshi Imami, Agnieszka Münster-Wandowski, Beatrix Fauler, Thorsten Mielke, Matthias Selbach, Markus Landthaler, Christian M

Cell type-dependent differential activation of ERK by oncogenic KRAS in colon cancer and intestinal epithelium

致癌KRAS在结肠癌和肠上皮细胞中对ERK的激活存在细胞类型依赖性差异。

Raphael Brandt ,Thomas Sell ,Mareen Lüthen ,Florian Uhlitz ,Bertram Klinger ,Pamela Riemer ,Claudia Giesecke-Thiel ,Silvia Schulze ,Ismail Amr El-Shimy ,Desiree Kunkel ,Beatrix Fauler ,Thorsten Mielke ,Norbert Mages ,Bernhard G Herrmann ,Christine Sers ,Nils Blüthgen ,Markus Morkel

Human iPSC-Derived Neural Progenitors Are an Effective Drug Discovery Model for Neurological mtDNA Disorders

人类 iPSC 衍生的神经祖细胞是治疗神经系统线粒体 DNA 疾病的有效药物发现模型

Carmen Lorenz, Pierre Lesimple, Raul Bukowiecki, Annika Zink, Gizem Inak, Barbara Mlody, Manvendra Singh, Marcus Semtner, Nancy Mah, Karine Auré, Megan Leong, Oleksandr Zabiegalov, Ekaterini-Maria Lyras, Vanessa Pfiffer, Beatrix Fauler, Jenny Eichhorst, Burkhard Wiesner, Norbert Huebner, Josef Prill

De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction

SLC25A24 的新生突变导致颅缝早闭综合征,伴有多毛症、早衰症和线粒体功能障碍

Nadja Ehmke, Luitgard Graul-Neumann, Lukasz Smorag, Rainer Koenig, Lara Segebrecht, Pilar Magoulas, Fernando Scaglia, Esra Kilic, Anna F Hennig, Nicolai Adolphs, Namrata Saha, Beatrix Fauler, Vera M Kalscheuer, Friederike Hennig, Janine Altmüller, Christian Netzer, Holger Thiele, Peter Nürnberg, Gök

Footprint-free human fetal foreskin derived iPSCs: A tool for modeling hepatogenesis associated gene regulatory networks

无足迹人类胎儿包皮来源的 iPSC:一种用于模拟肝发生相关基因调控网络的工具

Peggy Matz, Wasco Wruck, Beatrix Fauler, Diran Herebian, Thorsten Mielke, James Adjaye

Mitochondrial-associated cell death mechanisms are reset to an embryonic-like state in aged donor-derived iPS cells harboring chromosomal aberrations

在存在染色体畸变的老年供体衍生 iPS 细胞中,线粒体相关细胞死亡机制被重置为胚胎样状态

Alessandro Prigione, Amir M Hossini, Björn Lichtner, Akdes Serin, Beatrix Fauler, Matthias Megges, Rudi Lurz, Hans Lehrach, Eugenia Makrantonaki, Christos C Zouboulis, James Adjaye