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

MNX1 prevents somatostatin expression in human beta cells by repressing PERCC1.

MNX1 通过抑制 PERCC1 来阻止人类 β 细胞中生长抑素的表达。

Kobaisi Farah, Fouque Alexis, Ravassard Philippe, Albagli-Curiel Olivier, Scharfmann Raphael

HNF1A and A1CF coordinate a beta cell transcription-splicing axis that is disrupted in type 2 diabetes

HNF1A 和 A1CF 协调 β 细胞转录-剪接轴,该轴在 2 型糖尿病中受到破坏。

Edgar Bernardo,Matías Gonzalo De Vas,Diego Balboa,Mirabai Cuenca-Ardura,Sílvia Bonàs-Guarch,Mercè Planas-Fèlix,Fanny Mollandin,Miquel Torrens-Dinarès,Miguel Angel Maestro,Javier García-Hurtado,Sonia Moratinos,Philippe Ravassard,Haiqiang Dou,Holger Heyn,Alexander van Oudenaarden,Nathalie Groen,Eelco de Koning,Christian Conrad,Roland Eils,Santiago Vernia,Patrik Rorsman,Jorge Ferrer

Mutations in PSEN1 predispose inflammation in an astrocyte model of familial Alzheimer's disease through disrupted regulated intramembrane proteolysis

PSEN1基因突变通过破坏调控性膜内蛋白水解,使家族性阿尔茨海默病星形胶质细胞模型中的炎症易于发生。

Oliver J Ziff ,Gustavo Morrone Parfitt ,Sarah Jolly ,Jackie M Casey ,Lucy Granat ,Satinder Samra ,Núria Setó-Salvia ,Argyro Alatza ,Leela Phadke ,Benjamin Galet ,Philippe Ravassard ,Marie-Claude Potier ,John Hardy ,Dervis A Salih ,Paul Whiting ,Fiona Ducotterd ,Rickie Patani ,Selina Wray # ,Charles Arber #

C9ORF72 knockdown triggers FTD-like symptoms and cell pathology in mice

C9ORF72基因敲低可诱发小鼠额颞叶痴呆样症状和细胞病理改变。

Lopez-Herdoiza, Maria-Belen; Bauché, Stephanie; Wilmet, Baptiste; Le Duigou, Caroline; Roussel, Delphine; Frah, Magali; Béal, Jonas; Devely, Gabin; Boluda, Susana; Frick, Petra; Bouteiller, Delphine; Dussaud, Sébastien; Guillabert, Pierre; Dalle, Carine; Dumont, Magali; Camuzat, Agnes; Saracino, Dario; Barbier, Mathieu; Bruneteau, Gaelle; Ravassard, Phillippe; Neumann, Manuela; Nicole, Sophie; Le Ber, Isabelle; Brice, Alexis; Latouche, Morwena

The HASTER lncRNA promoter is a cis-acting transcriptional stabilizer of HNF1A

HASTER lncRNA 启动子是 HNF1A 的顺式转录稳定剂

Anthony Beucher, Irene Miguel-Escalada, Diego Balboa, Matías G De Vas, Miguel Angel Maestro, Javier Garcia-Hurtado, Aina Bernal, Roser Gonzalez-Franco, Pierfrancesco Vargiu, Holger Heyn, Philippe Ravassard, Sagrario Ortega, Jorge Ferrer

Transient regulation of focal adhesion via Tensin3 is required for nascent oligodendrocyte differentiation

通过 Tensin3 瞬时调节粘着斑是新生少突胶质细胞分化所必需的

Emeric Merour #, Hatem Hmidan #, Corentine Marie, Pierre-Henri Helou, Haiyang Lu, Antoine Potel, Jean-Baptiste Hure, Adrien Clavairoly, Yi Ping Shih, Salman Goudarzi, Sebastien Dussaud, Philippe Ravassard, Sassan Hafizi, Su Hao Lo, Bassem A Hassan, Carlos Parras

Does the Expression and Epigenetics of Genes Involved in Monogenic Forms of Parkinson's Disease Influence Sporadic Forms?

与单基因型帕金森病相关的基因表达和表观遗传是否会影响散发型帕金森病?

Lanore, Aymeric; Lesage, Suzanne; Mariani, Louise-Laure; Menon, Poornima Jayadev; Ravassard, Philippe; Cheval, Helene; Corti, Olga; Brice, Alexis; Corvol, Jean-Christophe

Using Inhibitory DREADDs to Silence LC Neurons in Monkeys

利用抑制性 DREADD 来沉默猴子的 LC 神经元

Pauline Perez, Estelle Chavret-Reculon, Philippe Ravassard, Sebastien Bouret

The Amyotrophic Lateral Sclerosis M114T PFN1 Mutation Deregulates Alternative Autophagy Pathways and Mitochondrial Homeostasis

肌萎缩侧索硬化症 M114T PFN1 突变导致替代自噬途径和线粒体稳态失调

Elisa Teyssou, Laura Chartier, Delphine Roussel, Nirma D Perera, Ivan Nemazanyy, Dominique Langui, Mélanie Albert, Thierry Larmonier, Safaa Saker, François Salachas, Pierre-François Pradat, Vincent Meininger, Philippe Ravassard, Francine Côté, Christian S Lobsiger, Séverine Boillée, Bradley J Turner

Neonatal diabetes mutations disrupt a chromatin pioneering function that activates the human insulin gene

新生儿糖尿病突变会破坏染色质先锋功能,而该功能会激活人类胰岛素基因。

Ildem Akerman,Miguel Angel Maestro,Elisa De Franco,Vanessa Grau,Sarah Flanagan,Javier García-Hurtado,Gerhard Mittler,Philippe Ravassard,Lorenzo Piemonti,Sian Ellard,Andrew T Hattersley,Jorge Ferrer