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I Nonaka

Showing results (241-250 of 503) with videos related to

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The Kumamoto Medical Journal|June 30, 1972
An electron microscopical study of the muscle in congenital muscular dystrophyI Nonaka, S Miyoshino, T Miike, et al.
Acta Neuropathologica|October 1, 1998
Fiber-type-dependent expression of adenovirus-mediated transgene in mouse skeletal muscle fibersY Hagiwara, A Ishii, I Nonaka, et al.
Journal of Neurology|January 1, 1985
Two siblings with multiple intracranial haemangiomatosis with calcificationA Tateno, A Matsui, N Sakuragawa, et al.
Muscle & Nerve|December 18, 2001
A new form of muscular dystrophy with mitochondrial structural abnormalitiesK Ikemoto-Tsuchiya, I Nishino, M Kawai, et al.
Muscle & Nerve|March 1, 1997
Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two familiesM Ozawa, I Nishino, S Horai, et al.
Neurology|January 28, 2009
Novel FHL1 mutations in fatal and benign reducing body myopathyS Shalaby, Y K Hayashi, I Nonaka, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 20, 2001
Novel androgen-dependent promoters direct expression of the C4b-binding protein alpha-chain gene in epididymisM I Nonaka, G Wang, T Mori, et al.
Chemical & Pharmaceutical Bulletin|April 20, 2001
Revised structure of cercidinin A, a novel ellagitannin having (R)-hexahydroxydiphenoyl esters at the 3,4-positions of glucopyranoseT Tanaka, G I Nonaka, M Ishimatsu, et al.
Acta Neuropathologica|January 1, 1995
Reducing bodies in distal myopathy with rimmed vacuole formationB H Kiyomoto, N Murakami, J Kishibayashi, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 1, 1989
[Ultrastructural immunocytochemical localization of electron-transport enzymes in mitochondrial myopathy]D L Song, T Sato, H Ujike, et al.
Pageof 51

Showing results (241-250 of 503) with videos related to

Sort By:
Pageof 51
The Kumamoto Medical Journal|June 30, 1972
An electron microscopical study of the muscle in congenital muscular dystrophyI Nonaka, S Miyoshino, T Miike, et al.
Acta Neuropathologica|October 1, 1998
Fiber-type-dependent expression of adenovirus-mediated transgene in mouse skeletal muscle fibersY Hagiwara, A Ishii, I Nonaka, et al.
Journal of Neurology|January 1, 1985
Two siblings with multiple intracranial haemangiomatosis with calcificationA Tateno, A Matsui, N Sakuragawa, et al.
Muscle & Nerve|December 18, 2001
A new form of muscular dystrophy with mitochondrial structural abnormalitiesK Ikemoto-Tsuchiya, I Nishino, M Kawai, et al.
Muscle & Nerve|March 1, 1997
Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two familiesM Ozawa, I Nishino, S Horai, et al.
Neurology|January 28, 2009
Novel FHL1 mutations in fatal and benign reducing body myopathyS Shalaby, Y K Hayashi, I Nonaka, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 20, 2001
Novel androgen-dependent promoters direct expression of the C4b-binding protein alpha-chain gene in epididymisM I Nonaka, G Wang, T Mori, et al.
Chemical & Pharmaceutical Bulletin|April 20, 2001
Revised structure of cercidinin A, a novel ellagitannin having (R)-hexahydroxydiphenoyl esters at the 3,4-positions of glucopyranoseT Tanaka, G I Nonaka, M Ishimatsu, et al.
Acta Neuropathologica|January 1, 1995
Reducing bodies in distal myopathy with rimmed vacuole formationB H Kiyomoto, N Murakami, J Kishibayashi, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 1, 1989
[Ultrastructural immunocytochemical localization of electron-transport enzymes in mitochondrial myopathy]D L Song, T Sato, H Ujike, et al.
Pageof 51