Results 201 to 210 of about 23,382 (212)

Lamin A/C Assembly Defects in LMNA-Congenital Muscular Dystrophy Is Responsible for the Increased Severity of the Disease Compared with Emery–Dreifuss Muscular Dystrophy

Cells, 2020
Anne T Bertrand, Astrid Brull, Louise Benarroch   +2 more
exaly  

Dilated cardiomyopathy causd by LMNA mutations

2012
MA ...
openaire   +1 more source

The Broad Spectrum of LMNA Cardiac Diseases: From Molecular Mechanisms to Clinical Phenotype

Frontiers in Physiology, 2020
Silvia Crasto, Elisa Di Pasquale
exaly  

LMNA (Laminopathy) Research

2021
openaire   +1 more source

Interplay of primary sequence, position and secondary RNA structure determines alternative splicing of LMNA in a pre-mature aging syndrome

Nucleic Acids Research, 2019
Tom Misteli
exaly  

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy

Nature Genetics, 2000
Sudhesh Kumar, Simon G Gregory, David J Lloyd   +2 more
exaly  

DNA Damage Response/TP53 Pathway Is Activated and Contributes to the Pathogenesis of Dilated Cardiomyopathy Associated With LMNA (Lamin A/C) Mutations

Circulation Research, 2019
Raffaella Lombardi, Luisa Mestroni, Cristian Coarfa   +2 more
exaly  

Gene symbol: LMNA. Disease: EDMD2.

Human genetics, 2005
A E, Arbustini Eloisa, Andrea, Pilotto, Michele, Pasotti, Maurizia, Grasso, Marta, Diegoli, Stefano, Ghio, Marilena, Tagliani, Luigi, Tavazzi   +7 more
openaire   +1 more source

Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in mice

Human Molecular Genetics, 2005
Colin L Stewart
exaly  

[LMNA gene and dilated cardiomyopathy].

Zhonghua xin xue guan bing za zhi, 2010
Li-ping, Sun, Jie-lin, Pu
openaire   +1 more source