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I Nonaka

Showing results (491-500 of 503) with videos related to

Pageof 51
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Neurology|March 24, 2004
POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in alpha-DGD S Kim, Y K Hayashi, H Matsumoto, et al.
European Journal of Neurology|November 2, 2011
Characterization of the Asian myopathy patients with VCP mutationsZ Shi, Y K Hayashi, S Mitsuhashi, et al.
Neurology|January 24, 2002
Mutation in the caveolin-3 gene causes a peculiar form of distal myopathyM Tateyama, M Aoki, I Nishino, et al.
Neurology|December 11, 2002
Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathyI Nishino, S Noguchi, K Murayama, et al.
Neurology|June 24, 2004
A new diagnostic test for VLCAD deficiency using immunohistochemistryY Ohashi, Y Hasegawa, K Murayama, et al.
Human Molecular Genetics|May 18, 2000
Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2AK Tagawa, C Taya, Y Hayashi, et al.
Neurology|June 27, 2002
Clinicopathological features of genetically confirmed Danon diseaseK Sugie, A Yamamoto, K Murayama, et al.
Nature|August 5, 1998
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophyK Kobayashi, Y Nakahori, M Miyake, et al.
Nature Genetics|May 20, 1998
Mutations in the integrin alpha7 gene cause congenital myopathyY K Hayashi, F L Chou, E Engvall, et al.
Nature|September 6, 2000
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)I Nishino, J Fu, K Tanji, et al.
Pageof 51

Showing results (491-500 of 503) with videos related to

Sort By:
Pageof 51
Neurology|March 24, 2004
POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in alpha-DGD S Kim, Y K Hayashi, H Matsumoto, et al.
European Journal of Neurology|November 2, 2011
Characterization of the Asian myopathy patients with VCP mutationsZ Shi, Y K Hayashi, S Mitsuhashi, et al.
Neurology|January 24, 2002
Mutation in the caveolin-3 gene causes a peculiar form of distal myopathyM Tateyama, M Aoki, I Nishino, et al.
Neurology|December 11, 2002
Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathyI Nishino, S Noguchi, K Murayama, et al.
Neurology|June 24, 2004
A new diagnostic test for VLCAD deficiency using immunohistochemistryY Ohashi, Y Hasegawa, K Murayama, et al.
Human Molecular Genetics|May 18, 2000
Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2AK Tagawa, C Taya, Y Hayashi, et al.
Neurology|June 27, 2002
Clinicopathological features of genetically confirmed Danon diseaseK Sugie, A Yamamoto, K Murayama, et al.
Nature|August 5, 1998
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophyK Kobayashi, Y Nakahori, M Miyake, et al.
Nature Genetics|May 20, 1998
Mutations in the integrin alpha7 gene cause congenital myopathyY K Hayashi, F L Chou, E Engvall, et al.
Nature|September 6, 2000
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)I Nishino, J Fu, K Tanji, et al.
Pageof 51