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

The actin assembly regulator toca-1 regulates collateral branching in C. elegans

肌动蛋白组装调节因子toca-1调控秀丽隐杆线虫的侧枝分支

Brinck, Anna; Dour, Scott; Nonet, M L

A toolkit for assembly of targeting clones for C. elegans transgenesis

用于组装秀丽隐杆线虫转基因靶向克隆的工具包

Knoebel, Emma; Dour, Scott; Nonet, Michael

Actin-microtubule cytoskeletal interplay mediated by MRTF-A/SRF signaling promotes dilated cardiomyopathy caused by LMNA mutations

MRTF-A/SRF 信号介导的肌动蛋白-微管细胞骨架相互作用促进 LMNA 突变引起的扩张型心肌病

Caroline Le Dour #, Maria Chatzifrangkeskou #, Coline Macquart #, Maria M Magiera, Cécile Peccate, Charlène Jouve, Laura Virtanen, Tiina Heliö, Katriina Aalto-Setälä, Silvia Crasto, Bruno Cadot, Déborah Cardoso, Nathalie Mougenot, Daniel Adesse, Elisa Di Pasquale, Jean-Sébastien Hulot, Pekka Taimen,

The non-muscle ADF/cofilin-1 controls sarcomeric actin filament integrity and force production in striated muscle laminopathies

非肌肉ADF/cofilin-1控制横纹肌层粘蛋白病中的肌节肌动蛋白丝完整性和力量产生

Nicolas Vignier ,Maria Chatzifrangkeskou ,Luca Pinton ,Hugo Wioland ,Thibaut Marais ,Mégane Lemaitre ,Caroline Le Dour ,Cécile Peccate ,Déborah Cardoso ,Alain Schmitt ,Wei Wu ,Maria-Grazia Biferi ,Naïra Naouar ,Coline Macquart ,Maud Beuvin ,Valérie Decostre ,Gisèle Bonne ,Guillaume Romet-Lemonne ,Howard J Worman ,Francesco Saverio Tedesco ,Antoine Jégou ,Antoine Muchir

Lipodystrophic syndromes due to LMNA mutations: recent developments on biomolecular aspects, pathophysiological hypotheses and therapeutic perspectives

由LMNA基因突变引起的脂肪营养不良综合征:生物分子方面、病理生理学假设和治疗前景的最新进展

Vigouroux, Corinne; Guénantin, Anne-Claire; Vatier, Camille; Capel, Emilie; Le Dour, Caroline; Afonso, Pauline; Bidault, Guillaume; Béréziat, Véronique; Lascols, Olivier; Capeau, Jacqueline; Briand, Nolwenn; Jéru, Isabelle

Extracellular matrix remodeling and transforming growth factor-β signaling abnormalities induced by lamin A/C variants that cause lipodystrophy

导致脂肪营养障碍的层蛋白 A/C 变异体诱发的细胞外基质重塑和转化生长因子-β 信号异常

Caroline Le Dour, Wei Wu, Véronique Béréziat, Jacqueline Capeau, Corinne Vigouroux, Howard J Worman

Decreased WNT/β-catenin signalling contributes to the pathogenesis of dilated cardiomyopathy caused by mutations in the lamin a/C gene

WNT/β-catenin 信号传导减弱是层蛋白 a/C 基因突变导致扩张型心肌病发病的原因之一

Caroline Le Dour, Coline Macquart, Fusako Sera, Shunichi Homma, Gisele Bonne, John P Morrow, Howard J Worman, Antoine Muchir

ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene

ERK1/2 直接作用于 CTGF/CCN2 的表达,从而介导由层粘蛋白 A/C 基因突变引起的心肌病中的心肌纤维化。

Chatzifrangkeskou, Maria; Le Dour, Caroline; Wu, Wei; Morrow, John P; Joseph, Leroy C; Beuvin, Maud; Sera, Fusako; Homma, Shunichi; Vignier, Nicolas; Mougenot, Nathalie; Bonne, Gisèle; Lipson, Kenneth E; Worman, Howard J; Muchir, Antoine

Anxiety and depressive symptoms and medical illness among adults with anxiety disorders

焦虑症患者的焦虑和抑郁症状以及躯体疾病

Niles, Andrea N; Dour, Halina J; Stanton, Annette L; Roy-Byrne, Peter P; Stein, Murray B; Sullivan, Greer; Sherbourne, Cathy D; Rose, Raphael D; Craske, Michelle G

Depletion of lamina-associated polypeptide 1 from cardiomyocytes causes cardiac dysfunction in mice.

心肌细胞中层粘连蛋白1的缺失会导致小鼠心脏功能障碍

Shin Ji-Yeon, Le Dour Caroline, Sera Fusako, Iwata Shinichi, Homma Shunichi, Joseph Leroy C, Morrow John P, Dauer William T, Worman Howard J