Results 211 to 217 of about 24,019 (217)

Hutchinson-Gilford Progeria Syndrome: A premature aging disease caused by LMNA gene mutations

Ageing Research Reviews, 2017
Susana Gonzalo, Raymond Kreienkamp, Peter Askjaer   +2 more
exaly  

Sensitivity to Entrectinib Associated With a Novel LMNA-NTRK1 Gene Fusion in Metastatic Colorectal Cancer

Journal of the National Cancer Institute, 2016
Andrea Sartore-Bianchi, Roberta Bosotti, Alessio Amatu   +2 more
exaly  

Mouse model carrying H222P- Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies

Human Molecular Genetics, 2005
Takuro Arimura, Anne Helbling-Leclerc, Yves Fromes   +2 more
exaly  

Modeling of LMNA-Related Dilated Cardiomyopathy Using Human Induced Pluripotent Stem Cells

Cells, 2019
Disheet A Shah, Laura Virtanen, Mostafa Kiamehr   +2 more
exaly  

A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation

Journal of Clinical Endocrinology and Metabolism, 2018
Iram Hussain, Nivedita Patni, Masako Ueda   +2 more
exaly  

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  

Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations

Journal of Clinical Endocrinology and Metabolism, 2009
Abhimanyu Garg, Giuseppe Novelli, Yanick J Crow   +2 more
exaly