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Y Sunada

Showing results (51-60 of 77) with videos related to

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Human Mutation|January 1, 1995
Haplotype analysis in gelsolin-related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and JapanT Paunio, Y Sunada, S Kiuru, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|December 26, 2008
Caveolin-3 regulates myostatin signaling. Mini-reviewY Ohsawa, T Okada, A Kuga, et al.
Journal of the Neurological Sciences|November 1, 1994
Cerebellar ataxia and polyneuropathy in a patient with IgM M-protein specific to the Gal(beta 1-3)GalNAc epitopeS Hitoshi, S Kusunoki, A Chiba, et al.
Human Molecular Genetics|October 1, 1994
Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoformJ A Rafael, Y Sunada, N M Cole, et al.
FEBS Letters|February 13, 2001
Structural organization, complete genomic sequences and mutational analyses of the Fukuyama-type congenital muscular dystrophy gene, fukutinK Kobayashi, J Sasaki, E Kondo-Iida, et al.
Human Molecular Genetics|February 13, 2001
Transgenic mice expressing mutant caveolin-3 show severe myopathy associated with increased nNOS activityY Sunada, H Ohi, A Hase, et al.
Gene Therapy|March 8, 2008
Atelocollagen-mediated local and systemic applications of myostatin-targeting siRNA increase skeletal muscle massN Kinouchi, Y Ohsawa, N Ishimaru, et al.
The New England Journal of Medicine|February 8, 1996
Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathyR Fadic, Y Sunada, A J Waclawik, et al.
Muscle & Nerve|May 1, 1995
Three-dimensional MR imaging of brain surface anomalies in Fukuyama-type congenital muscular dystrophyT Toda, T Watanabe, K Matsumura, et al.
Gene Therapy|November 1, 1996
In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genesP R Clemens, S Kochanek, Y Sunada, et al.
Pageof 8

Showing results (51-60 of 77) with videos related to

Sort By:
Pageof 8
Human Mutation|January 1, 1995
Haplotype analysis in gelsolin-related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and JapanT Paunio, Y Sunada, S Kiuru, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|December 26, 2008
Caveolin-3 regulates myostatin signaling. Mini-reviewY Ohsawa, T Okada, A Kuga, et al.
Journal of the Neurological Sciences|November 1, 1994
Cerebellar ataxia and polyneuropathy in a patient with IgM M-protein specific to the Gal(beta 1-3)GalNAc epitopeS Hitoshi, S Kusunoki, A Chiba, et al.
Human Molecular Genetics|October 1, 1994
Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoformJ A Rafael, Y Sunada, N M Cole, et al.
FEBS Letters|February 13, 2001
Structural organization, complete genomic sequences and mutational analyses of the Fukuyama-type congenital muscular dystrophy gene, fukutinK Kobayashi, J Sasaki, E Kondo-Iida, et al.
Human Molecular Genetics|February 13, 2001
Transgenic mice expressing mutant caveolin-3 show severe myopathy associated with increased nNOS activityY Sunada, H Ohi, A Hase, et al.
Gene Therapy|March 8, 2008
Atelocollagen-mediated local and systemic applications of myostatin-targeting siRNA increase skeletal muscle massN Kinouchi, Y Ohsawa, N Ishimaru, et al.
The New England Journal of Medicine|February 8, 1996
Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathyR Fadic, Y Sunada, A J Waclawik, et al.
Muscle & Nerve|May 1, 1995
Three-dimensional MR imaging of brain surface anomalies in Fukuyama-type congenital muscular dystrophyT Toda, T Watanabe, K Matsumura, et al.
Gene Therapy|November 1, 1996
In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genesP R Clemens, S Kochanek, Y Sunada, et al.
Pageof 8