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Showing results (361-370 of 503) with videos related to

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Nature Genetics|October 4, 2000
Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotesK Inoue, K Nakada, A Ogura, et al.
Muscle & Nerve. Supplement|April 12, 2013
Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analysesK Arahata, T Ishihara, H Fukunaga, et al.
Neuroscience Letters|December 31, 1998
Up-regulation of glial cell line-derived neurotrophic factor (GDNF) expression in regenerating muscle fibers in neuromuscular diseasesH Suzuki, A Hase, B Y Kim, et al.
Neuromuscular Disorders : NMD|November 26, 1998
Presence of emerinopathy in cases of rigid spine syndromeS Kubo, T Tsukahara, M Takemitsu, et al.
Neurology|July 11, 2001
Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophyY K Hayashi, M Ogawa, K Tagawa, et al.
Glia|July 19, 2001
Schwann cell myelination occurred without basal lamina formation in laminin alpha2 chain-null mutant (dy3K/dy3K) miceM Nakagawa, Y Miyagoe-Suzuki, K Ikezoe, et al.
Journal of the Neurological Sciences|January 1, 1995
Fatal reducing body myopathy. Ultrastructural and immunohistochemical observationsB H Kiyomoto, N Murakami, Y Kobayashi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Molecular pathomechanism of distal myopathy with rimmed vacuolesI Nishino, May Christine V Malicdan, K Murayama, et al.
Human Pathology|January 1, 1990
Congenital nemaline myopathy with dilated cardiomyopathy: an autopsy studyH Ishibashi-Ueda, M Imakita, C Yutani, et al.
Cellular Immunology|November 1, 1986
Mitogenic heparin-binding lectin-like protein from cloned thymic myoid cellsI Kamo, S Furukawa, S Akazawa, et al.
Pageof 51

Showing results (361-370 of 503) with videos related to

Sort By:
Pageof 51
Nature Genetics|October 4, 2000
Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotesK Inoue, K Nakada, A Ogura, et al.
Muscle & Nerve. Supplement|April 12, 2013
Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analysesK Arahata, T Ishihara, H Fukunaga, et al.
Neuroscience Letters|December 31, 1998
Up-regulation of glial cell line-derived neurotrophic factor (GDNF) expression in regenerating muscle fibers in neuromuscular diseasesH Suzuki, A Hase, B Y Kim, et al.
Neuromuscular Disorders : NMD|November 26, 1998
Presence of emerinopathy in cases of rigid spine syndromeS Kubo, T Tsukahara, M Takemitsu, et al.
Neurology|July 11, 2001
Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophyY K Hayashi, M Ogawa, K Tagawa, et al.
Glia|July 19, 2001
Schwann cell myelination occurred without basal lamina formation in laminin alpha2 chain-null mutant (dy3K/dy3K) miceM Nakagawa, Y Miyagoe-Suzuki, K Ikezoe, et al.
Journal of the Neurological Sciences|January 1, 1995
Fatal reducing body myopathy. Ultrastructural and immunohistochemical observationsB H Kiyomoto, N Murakami, Y Kobayashi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Molecular pathomechanism of distal myopathy with rimmed vacuolesI Nishino, May Christine V Malicdan, K Murayama, et al.
Human Pathology|January 1, 1990
Congenital nemaline myopathy with dilated cardiomyopathy: an autopsy studyH Ishibashi-Ueda, M Imakita, C Yutani, et al.
Cellular Immunology|November 1, 1986
Mitogenic heparin-binding lectin-like protein from cloned thymic myoid cellsI Kamo, S Furukawa, S Akazawa, et al.
Pageof 51