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Steven H Laval

Showing results (11-20 of 18) with videos related to

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Human Gene Therapy|February 26, 2009
Efficient and fast functional screening of microdystrophin constructs in vivo and in vitro for therapy of duchenne muscular dystrophyLouise H Jørgensen, Nancy Larochelle, Kristian Orlopp, et al.
Brain : a Journal of Neurology|June 5, 2016
Identification of mutations in the MYO9A gene in patients with congenital myasthenic syndromeEmily O'Connor, Ana Töpf, Juliane S Müller, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 23, 2006
AHNAK, a novel component of the dysferlin protein complex, redistributes to the cytoplasm with dysferlin during skeletal muscle regenerationYanchao Huang, Steven H Laval, Alexandra van Remoortere, et al.
Neuromuscular Disorders : NMD|November 18, 2005
The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient miceMaja von der Hagen, Steven H Laval, Lynsey M Cree, et al.
Brain : a Journal of Neurology|December 28, 2010
A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophyDebbie Hicks, Anna Sarkozy, Nuria Muelas, et al.
Journal of Neuromuscular Diseases|February 13, 2016
Mutations in the Mitochondrial Citrate Carrier SLC25A1 are Associated with Impaired Neuromuscular TransmissionAmina Chaouch, Vito Porcelli, Daniel Cox, et al.
Brain : a Journal of Neurology|June 22, 2014
Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophySophie Nicole, Amina Chaouch, Torberg Torbergsen, et al.
American Journal of Human Genetics|February 12, 2011
Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defectJan Senderek, Juliane S Müller, Marina Dusl, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Human Gene Therapy|February 26, 2009
Efficient and fast functional screening of microdystrophin constructs in vivo and in vitro for therapy of duchenne muscular dystrophyLouise H Jørgensen, Nancy Larochelle, Kristian Orlopp, et al.
Brain : a Journal of Neurology|June 5, 2016
Identification of mutations in the MYO9A gene in patients with congenital myasthenic syndromeEmily O'Connor, Ana Töpf, Juliane S Müller, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 23, 2006
AHNAK, a novel component of the dysferlin protein complex, redistributes to the cytoplasm with dysferlin during skeletal muscle regenerationYanchao Huang, Steven H Laval, Alexandra van Remoortere, et al.
Neuromuscular Disorders : NMD|November 18, 2005
The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient miceMaja von der Hagen, Steven H Laval, Lynsey M Cree, et al.
Brain : a Journal of Neurology|December 28, 2010
A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophyDebbie Hicks, Anna Sarkozy, Nuria Muelas, et al.
Journal of Neuromuscular Diseases|February 13, 2016
Mutations in the Mitochondrial Citrate Carrier SLC25A1 are Associated with Impaired Neuromuscular TransmissionAmina Chaouch, Vito Porcelli, Daniel Cox, et al.
Brain : a Journal of Neurology|June 22, 2014
Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophySophie Nicole, Amina Chaouch, Torberg Torbergsen, et al.
American Journal of Human Genetics|February 12, 2011
Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defectJan Senderek, Juliane S Müller, Marina Dusl, et al.
Pageof 2