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K N North

Showing results (31-40 of 48) with videos related to

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Cell Motility and the Cytoskeleton|May 18, 2004
C2C12 co-culture on a fibroblast substratum enables sustained survival of contractile, highly differentiated myotubes with peripheral nuclei and adult fast myosin expressionS T Cooper, A L Maxwell, E Kizana, et al.
Molecular Biology of the Cell|August 22, 2014
Calpain cleavage within dysferlin exon 40a releases a synaptotagmin-like module for membrane repairG M I Redpath, N Woolger, A K Piper, et al.
Neurology|February 1, 1996
Cognitive dysfunction as the major presenting feature of Becker's muscular dystrophyK N North, G Miller, S T Iannaccone, et al.
Annals of Neurology|September 18, 2001
Nemaline myopathy: a clinical study of 143 casesM M Ryan, C Schnell, C D Strickland, et al.
Neuromuscular Disorders : NMD|August 6, 2003
Deficiency of the syntrophins and alpha-dystrobrevin in patients with inherited myopathyK J Jones, A G Compton, N Yang, et al.
Familial Cancer|July 26, 2012
Parent-of-origin in individuals with familial neurofibromatosis type 1 and optic pathway gliomasK J Johnson, M J Fisher, R L Listernick, et al.
Neuromuscular Disorders : NMD|January 22, 2002
Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profileC G Bönnemann, J Wong, K J Jones, et al.
Neurology|December 28, 2007
Diagnosis and etiology of congenital muscular dystrophyR A Peat, J M Smith, A G Compton, et al.
International Journal of Obesity (2005)|March 16, 2017
Exploring the relationship between α-actinin-3 deficiency and obesity in mice and humansP J Houweling, Y D Berman, N Turner, et al.
Neurology|September 11, 2002
Gliomas presenting after age 10 in individuals with neurofibromatosis type 1 (NF1)D H Gutmann, S A Rasmussen, P Wolkenstein, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Cell Motility and the Cytoskeleton|May 18, 2004
C2C12 co-culture on a fibroblast substratum enables sustained survival of contractile, highly differentiated myotubes with peripheral nuclei and adult fast myosin expressionS T Cooper, A L Maxwell, E Kizana, et al.
Molecular Biology of the Cell|August 22, 2014
Calpain cleavage within dysferlin exon 40a releases a synaptotagmin-like module for membrane repairG M I Redpath, N Woolger, A K Piper, et al.
Neurology|February 1, 1996
Cognitive dysfunction as the major presenting feature of Becker's muscular dystrophyK N North, G Miller, S T Iannaccone, et al.
Annals of Neurology|September 18, 2001
Nemaline myopathy: a clinical study of 143 casesM M Ryan, C Schnell, C D Strickland, et al.
Neuromuscular Disorders : NMD|August 6, 2003
Deficiency of the syntrophins and alpha-dystrobrevin in patients with inherited myopathyK J Jones, A G Compton, N Yang, et al.
Familial Cancer|July 26, 2012
Parent-of-origin in individuals with familial neurofibromatosis type 1 and optic pathway gliomasK J Johnson, M J Fisher, R L Listernick, et al.
Neuromuscular Disorders : NMD|January 22, 2002
Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profileC G Bönnemann, J Wong, K J Jones, et al.
Neurology|December 28, 2007
Diagnosis and etiology of congenital muscular dystrophyR A Peat, J M Smith, A G Compton, et al.
International Journal of Obesity (2005)|March 16, 2017
Exploring the relationship between α-actinin-3 deficiency and obesity in mice and humansP J Houweling, Y D Berman, N Turner, et al.
Neurology|September 11, 2002
Gliomas presenting after age 10 in individuals with neurofibromatosis type 1 (NF1)D H Gutmann, S A Rasmussen, P Wolkenstein, et al.
Pageof 5