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Showing results (431-440 of 503) with videos related to

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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 24, 2008
Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in JapanM N Astejada, K Goto, A Nagano, et al.
Neurology|September 6, 2007
Reduced cell anchorage may cause sarcolemma-specific collagen VI deficiency in Ullrich diseaseG Kawahara, M Okada, N Morone, et al.
Rinsho Shinkeigaku = Clinical Neurology|March 22, 2001
[Muscle involvement of Stormorken's syndrome]M Mizobuchi, C Tanaka, K Sako, et al.
Annals of Neurology|March 1, 1994
Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomesY Kawakami, R Sakuta, K Hashimoto, et al.
Diabetes Care|November 1, 1996
Clinical picture of a case of diabetes with mitochondrial tRNA mutation at position 3271Y Suzuki, K Tsukuda, Y Atsumi, et al.
Rinsho Shinkeigaku = Clinical Neurology|November 5, 1999
[Hepatic involvement in a case of lysosomal glycogen storage disease with normal acid maltase]S Matsumoto, T Yamada, K Tanaka, et al.
Neuromuscular Disorders : NMD|May 1, 1994
Immunohistochemical analysis of perforin and granzyme A in inflammatory myopathiesS Orimo, R Koga, K Goto, et al.
No to Hattatsu = Brain and Development|January 1, 1992
[Ergometric and pathologic study of a family with complex I deficiency]M Tojo, N Ogawa, M Takeuchi, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|June 16, 2001
Maximal and submaximal forces of slow fibers in human soleus after bed restK Yamashita-Goto, R Okuyama, M Honda, et al.
The Journal of Cell Biology|April 18, 1998
MKBP, a novel member of the small heat shock protein family, binds and activates the myotonic dystrophy protein kinaseA Suzuki, Y Sugiyama, Y Hayashi, et al.
Pageof 51

Showing results (431-440 of 503) with videos related to

Sort By:
Pageof 51
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 24, 2008
Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in JapanM N Astejada, K Goto, A Nagano, et al.
Neurology|September 6, 2007
Reduced cell anchorage may cause sarcolemma-specific collagen VI deficiency in Ullrich diseaseG Kawahara, M Okada, N Morone, et al.
Rinsho Shinkeigaku = Clinical Neurology|March 22, 2001
[Muscle involvement of Stormorken's syndrome]M Mizobuchi, C Tanaka, K Sako, et al.
Annals of Neurology|March 1, 1994
Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomesY Kawakami, R Sakuta, K Hashimoto, et al.
Diabetes Care|November 1, 1996
Clinical picture of a case of diabetes with mitochondrial tRNA mutation at position 3271Y Suzuki, K Tsukuda, Y Atsumi, et al.
Rinsho Shinkeigaku = Clinical Neurology|November 5, 1999
[Hepatic involvement in a case of lysosomal glycogen storage disease with normal acid maltase]S Matsumoto, T Yamada, K Tanaka, et al.
Neuromuscular Disorders : NMD|May 1, 1994
Immunohistochemical analysis of perforin and granzyme A in inflammatory myopathiesS Orimo, R Koga, K Goto, et al.
No to Hattatsu = Brain and Development|January 1, 1992
[Ergometric and pathologic study of a family with complex I deficiency]M Tojo, N Ogawa, M Takeuchi, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|June 16, 2001
Maximal and submaximal forces of slow fibers in human soleus after bed restK Yamashita-Goto, R Okuyama, M Honda, et al.
The Journal of Cell Biology|April 18, 1998
MKBP, a novel member of the small heat shock protein family, binds and activates the myotonic dystrophy protein kinaseA Suzuki, Y Sugiyama, Y Hayashi, et al.
Pageof 51