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Showing results (81-90 of 87) with videos related to

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Reviews of Physiology, Biochemistry and Pharmacology|July 9, 1999
The titin cDNA sequence and partial genomic sequences: insights into the molecular genetics, cell biology and physiology of the titin filament systemB Kolmerer, C C Witt, A Freiburg, et al.
Nature Genetics|December 1, 1995
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathyG Bonne, L Carrier, J Bercovici, et al.
Neuromuscular Disorders : NMD|March 21, 2001
Nebulin expression in patients with nemaline myopathyJ Gurgel-Giannetti, U Reed, M L Bang, et al.
Circulation Research|March 1, 1997
Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathyL Carrier, G Bonne, E Bährend, et al.
Neuromuscular Disorders : NMD|February 5, 2013
In vivo and in vitro investigations of heterozygous nebulin knock-out mice disclose a mild skeletal muscle phenotypeC Gineste, J M De Winter, C Kohl, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 1999
Mutations in the nebulin gene associated with autosomal recessive nemaline myopathyK Pelin, P Hilpelä, K Donner, et al.
Journal of Neuroimmunology|March 6, 2016
Titin antibodies in "seronegative" myasthenia gravis--A new role for an old antigenC Stergiou, K Lazaridis, V Zouvelou, et al.
Pageof 9

Showing results (81-90 of 87) with videos related to

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Pageof 9
You have reached the last page of results.This site can display upto 87 results.
Reviews of Physiology, Biochemistry and Pharmacology|July 9, 1999
The titin cDNA sequence and partial genomic sequences: insights into the molecular genetics, cell biology and physiology of the titin filament systemB Kolmerer, C C Witt, A Freiburg, et al.
Nature Genetics|December 1, 1995
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathyG Bonne, L Carrier, J Bercovici, et al.
Neuromuscular Disorders : NMD|March 21, 2001
Nebulin expression in patients with nemaline myopathyJ Gurgel-Giannetti, U Reed, M L Bang, et al.
Circulation Research|March 1, 1997
Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathyL Carrier, G Bonne, E Bährend, et al.
Neuromuscular Disorders : NMD|February 5, 2013
In vivo and in vitro investigations of heterozygous nebulin knock-out mice disclose a mild skeletal muscle phenotypeC Gineste, J M De Winter, C Kohl, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 1999
Mutations in the nebulin gene associated with autosomal recessive nemaline myopathyK Pelin, P Hilpelä, K Donner, et al.
Journal of Neuroimmunology|March 6, 2016
Titin antibodies in "seronegative" myasthenia gravis--A new role for an old antigenC Stergiou, K Lazaridis, V Zouvelou, et al.
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