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

Harnessing Distinct Tissue-Resident Immune Niches via S100A9/TLR4 Improves Ketone, Lipid, and Glucose Metabolism

利用S100A9/TLR4调控不同的组织驻留免疫微环境可改善酮体、脂质和葡萄糖代谢

Giulia Lucibello ,Gloria Ursino ,Pryscila D S Teixeira ,Szabolcs Zahoran ,Francesca Fanuele ,Marinos Kallikourdis ,Florian Visentin ,Christelle Veyrat-Durebex ,Ariane Widmer ,Yibo Wu ,Marco Cremonesi ,Claes B Wollheim ,Perrine Castets ,Giorgio Ramadori ,Roberto Coppari

mTORC1 and PKB/Akt control the muscle response to denervation by regulating autophagy and HDAC4

mTORC1 和 PKB/Akt 通过调节自噬和 HDAC4 来控制肌肉对失神经支配的反应

Perrine Castets, Nathalie Rion, Marine Théodore, Denis Falcetta, Shuo Lin, Markus Reischl, Franziska Wild, Laurent Guérard, Christopher Eickhorst, Marielle Brockhoff, Maitea Guridi, Chikwendu Ibebunjo, Joseph Cruz, Michael Sinnreich, Rüdiger Rudolf, David J Glass, Markus A Rüegg

mTORC2 affects the maintenance of the muscle stem cell pool

mTORC2 影响肌肉干细胞库的维持

Nathalie Rion, Perrine Castets, Shuo Lin, Leonie Enderle, Judith R Reinhard, Markus A Rüegg

mTOR controls embryonic and adult myogenesis via mTORC1

mTOR 通过 mTORC1 控制胚胎和成人肌肉生成

Nathalie Rion, Perrine Castets, Shuo Lin, Leonie Enderle, Judith R Reinhard, Christopher Eickhorst, Markus A Rüegg

Targeting deregulated AMPK/mTORC1 pathways improves muscle function in myotonic dystrophy type I

靶向失调的 AMPK/mTORC1 通路可改善 I 型强直性肌营养不良症患者的肌肉功能

Marielle Brockhoff, Nathalie Rion, Kathrin Chojnowska, Tatiana Wiktorowicz, Christopher Eickhorst, Beat Erne, Stephan Frank, Corrado Angelini, Denis Furling, Markus A Rüegg, Michael Sinnreich, Perrine Castets

Differential response of skeletal muscles to mTORC1 signaling during atrophy and hypertrophy

骨骼肌在萎缩和肥大过程中对 mTORC1 信号的不同反应

C Florian Bentzinger #, Shuo Lin #, Klaas Romanino, Perrine Castets, Maitea Guridi, Serge Summermatter, Christoph Handschin, Lionel A Tintignac, Michael N Hall, Markus A Rüegg

Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy

硒蛋白 N 失活导致小鼠肌肉应激敏感性增强:SEPN1 相关肌病的哺乳动物模型

Mathieu Rederstorff, Perrine Castets, Sandrine Arbogast, Jeanne Lainé, Stéphane Vassilopoulos, Maud Beuvin, Odile Dubourg, Alban Vignaud, Arnaud Ferry, Alain Krol, Valérie Allamand, Pascale Guicheney, Ana Ferreiro, Alain Lescure

Mutations in the selenocysteine insertion sequence-binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans

硒半胱氨酸插入序列结合蛋白 2 基因突变导致人类多系统硒蛋白缺乏症

Erik Schoenmakers, Maura Agostini, Catherine Mitchell, Nadia Schoenmakers, Laura Papp, Odelia Rajanayagam, Raja Padidela, Lourdes Ceron-Gutierrez, Rainer Doffinger, Claudia Prevosto, Jian'an Luan, Sergio Montano, Jun Lu, Mireille Castanet, Nick Clemons, Matthijs Groeneveld, Perrine Castets, Mahsa Ka

Selenoprotein N is dynamically expressed during mouse development and detected early in muscle precursors

硒蛋白 N 在小鼠发育过程中动态表达,并在肌肉前体中早期检测到

Perrine Castets, Svetlana Maugenre, Corine Gartioux, Mathieu Rederstorff, Alain Krol, Alain Lescure, Shahragim Tajbakhsh, Valérie Allamand, Pascale Guicheney