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日期影响因子

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

影响因子:4.5

doi:10.1080/19491034.2018.1456217

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

发表日期：2018

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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。

期刊:Human Molecular Genetics

影响因子:3.2

doi:10.1093/hmg/ddw090

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

发表日期：2016

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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

影响因子:4.5

doi:10.4161/nucl.29227

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

细胞生物学

发表日期：2014

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The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress

LMNA基因中的R439C突变会导致层粘蛋白寡聚化和对氧化应激的敏感性。

期刊:Journal of Cellular and Molecular Medicine

影响因子:4.2

doi:10.1111/j.1582-4934.2009.00690.x

Verstraeten, Valerie L R M; Caputo, Sandrine; van Steensel, Maurice A M; Duband-Goulet, Isabelle; Zinn-Justin, Sophie; Kamps, Miriam; Kuijpers, Helma J H; Ostlund, Cecilia; Worman, Howard J; Briedé, Jacob J; Le Dour, Caroline; Marcelis, Carlo L M; van Geel, Michel; Steijlen, Peter M; van den Wijngaard, Arthur; Ramaekers, Frans C S; Broers, Jos L V

发表日期：2009

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