Results 111 to 120 of about 864,168 (128)

P.145 Identification of potential genetic modifiers underlying phenotypic variability in a French family with striated muscle laminopathies

Neuromuscular Disorders, 2022
I Nelson, R Ben Yaou, M Beuvin
exaly  

Nesprin-1 LINC complexes recruit microtubule cytoskeleton proteins and drive pathology in Lmna-mutant striated muscle.

Human Molecular Genetics, 2023
Bruno Cadot, Colin L Stewart, Brian Burke   +2 more
exaly  

Development of gene therapy for striated muscle laminopathy

2022
Okubo, Mariko, Brull, Astrid, Beuvin, Maud, Bonne, Gisèle, Bertrand, Anne T   +4 more
openaire   +1 more source

G.P.4.04 Lamin A/C gene mutation as a cause of dropped head syndrome. Extending the striated muscle laminopathies

Neuromuscular Disorders, 2006
A. Nascimento, J. Colomer, J. Demay, R. Ben Yaou, P. Richard, G. Bonne   +5 more
openaire   +1 more source

Striated muscle laminopathies: Modifier variants

2022
openaire   +1 more source

miRNA-processing pathway is impaired in striated muscle laminopathies

2022
Brull, Astrid, Beuvin, Maud, Nelson, Isabelle, Bonne, Gisèle, Bertrand, Anne T.   +4 more
openaire   +1 more source

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Frontiers in Physiology, 2018
Francesco Saverio Tedesco, Peter S Zammit, Sara M Maffioletti   +2 more
exaly  

Insights in the pathophysiological mechanisms of striated muscle Laminopathies

2023
openaire   +2 more sources

THE DOUBLE ARRAY OF FILAMENTS IN CROSS-STRIATED MUSCLE

The Journal of Biophysical and Biochemical Cytology, 1957
H E Huxley
exaly  

Muscle development, regeneration and laminopathies: how lamins or lamina-associated proteins can contribute to muscle development, regeneration and disease

Cellular and Molecular Life Sciences, 2012
Ryszard Rzepecki, Magdalena Zaremba-Czogalla, Magda Dubińska-Magiera   +2 more
exaly