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Showing results (441-450 of 503) with videos related to

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Annals of Neurology|November 1, 1990
Quadriceps myopathy: forme fruste of Becker muscular dystrophyN Sunohara, K Arahata, E P Hoffman, et al.
Neuromuscular Disorders : NMD|March 14, 2000
Genetic heterogeneity in three Chinese children with Fukuyama congenital muscular dystrophyY J Jong, K Kobayashi, T Toda, et al.
Neurology|February 26, 2004
Ullrich disease due to deficiency of collagen VI in the sarcolemmaH Ishikawa, K Sugie, K Murayama, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|March 20, 2004
Tension- and afferent input-associated responses of neuromuscular system of rats to hindlimb unloading and/or tenotomyF Kawano, A Ishihara, J L Stevens, et al.
Nature|June 30, 1988
Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptideK Arahata, S Ishiura, T Ishiguro, et al.
Neuropediatrics|February 1, 1985
Successful carnitine treatment in two siblings having lipid storage myopathy with hypertrophic cardiomyopathyT Matsuishi, K Hirata, K Terasawa, et al.
Immunogenetics|July 9, 2005
Unprecedented intraspecific diversity of the MHC class I region of a teleost medaka, Oryzias latipesKentaro Tsukamoto, Shinpei Hayashi, Megumi Y Matsuo, et al.
Human Molecular Genetics|September 5, 2001
The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscleC Matsuda, Y K Hayashi, M Ogawa, et al.
Human Genetics|November 3, 1998
Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD)K Kobayashi, Y Nakahori, K Mizuno, et al.
No to Hattatsu = Brain and Development|July 1, 1990
[A case of complex I deficiency with episodic respiratory distress]J Tohyama, K Torigoe, S Sato, et al.
Pageof 51

Showing results (441-450 of 503) with videos related to

Sort By:
Pageof 51
Annals of Neurology|November 1, 1990
Quadriceps myopathy: forme fruste of Becker muscular dystrophyN Sunohara, K Arahata, E P Hoffman, et al.
Neuromuscular Disorders : NMD|March 14, 2000
Genetic heterogeneity in three Chinese children with Fukuyama congenital muscular dystrophyY J Jong, K Kobayashi, T Toda, et al.
Neurology|February 26, 2004
Ullrich disease due to deficiency of collagen VI in the sarcolemmaH Ishikawa, K Sugie, K Murayama, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|March 20, 2004
Tension- and afferent input-associated responses of neuromuscular system of rats to hindlimb unloading and/or tenotomyF Kawano, A Ishihara, J L Stevens, et al.
Nature|June 30, 1988
Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptideK Arahata, S Ishiura, T Ishiguro, et al.
Neuropediatrics|February 1, 1985
Successful carnitine treatment in two siblings having lipid storage myopathy with hypertrophic cardiomyopathyT Matsuishi, K Hirata, K Terasawa, et al.
Immunogenetics|July 9, 2005
Unprecedented intraspecific diversity of the MHC class I region of a teleost medaka, Oryzias latipesKentaro Tsukamoto, Shinpei Hayashi, Megumi Y Matsuo, et al.
Human Molecular Genetics|September 5, 2001
The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscleC Matsuda, Y K Hayashi, M Ogawa, et al.
Human Genetics|November 3, 1998
Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD)K Kobayashi, Y Nakahori, K Mizuno, et al.
No to Hattatsu = Brain and Development|July 1, 1990
[A case of complex I deficiency with episodic respiratory distress]J Tohyama, K Torigoe, S Sato, et al.
Pageof 51