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I Nonaka

Showing results (411-420 of 503) with videos related to

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Muscle & Nerve|January 14, 1998
A new congenital muscular dystrophy with mitochondrial structural abnormalitiesI Nishino, O Kobayashi, Y Goto, et al.
Biochemical and Biophysical Research Communications|June 24, 1998
Tissue-specific involvement of multiple mitochondrial DNA deletions in familial mitochondrial myopathyS Nishizuka, G Tamura, Y Goto, et al.
Advances in Space Research : the Official Journal of the Committee on Space Research (COSPAR)|January 18, 2003
Gravitational unloading effects on muscle fiber size, phenotype and myonuclear numberY Ohira, T Yoshinaga, T Nomura, et al.
Neuromuscular Disorders : NMD|August 6, 2003
Beyond LGMD1A: myotilin is a component of central core lesions and nemaline rodsR Schröder, J Reimann, P Salmikangas, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome and NADH-CoQ reductase deficiencyM Kobayashi, H Morishita, N Sugiyama, et al.
No to Hattatsu = Brain and Development|September 16, 1999
[A sporadic case of Charcot-Marie-Tooth disease type 1 A associated with a duplication in chromosome 17 p11.2-p12]M Inoue, M Kojima, H Aikoh, et al.
Nature Medicine|August 2, 2001
Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNAK Nakada, K Inoue, T Ono, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Frequent mutations in Japanese patients with acid maltase deficiencyS Tsujino, M Huie, N Kanazawa, et al.
Journal of Biochemistry|April 1, 1990
Antibody against the C-terminal portion of dystrophin crossreacts with the 400 kDa protein in the pia mater of dystrophin-deficient mdx mouse brainS Ishiura, K Arahata, T Tsukahara, et al.
Journal of the Neurological Sciences|December 1, 1995
Congenital hypomyelination neuropathy: decreased expression of the P2 protein in peripheral nerve with normal DNA sequence of the coding regionY Sawaishi, K Hayasaka, A Goto, et al.
Pageof 51

Showing results (411-420 of 503) with videos related to

Sort By:
Pageof 51
Muscle & Nerve|January 14, 1998
A new congenital muscular dystrophy with mitochondrial structural abnormalitiesI Nishino, O Kobayashi, Y Goto, et al.
Biochemical and Biophysical Research Communications|June 24, 1998
Tissue-specific involvement of multiple mitochondrial DNA deletions in familial mitochondrial myopathyS Nishizuka, G Tamura, Y Goto, et al.
Advances in Space Research : the Official Journal of the Committee on Space Research (COSPAR)|January 18, 2003
Gravitational unloading effects on muscle fiber size, phenotype and myonuclear numberY Ohira, T Yoshinaga, T Nomura, et al.
Neuromuscular Disorders : NMD|August 6, 2003
Beyond LGMD1A: myotilin is a component of central core lesions and nemaline rodsR Schröder, J Reimann, P Salmikangas, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome and NADH-CoQ reductase deficiencyM Kobayashi, H Morishita, N Sugiyama, et al.
No to Hattatsu = Brain and Development|September 16, 1999
[A sporadic case of Charcot-Marie-Tooth disease type 1 A associated with a duplication in chromosome 17 p11.2-p12]M Inoue, M Kojima, H Aikoh, et al.
Nature Medicine|August 2, 2001
Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNAK Nakada, K Inoue, T Ono, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Frequent mutations in Japanese patients with acid maltase deficiencyS Tsujino, M Huie, N Kanazawa, et al.
Journal of Biochemistry|April 1, 1990
Antibody against the C-terminal portion of dystrophin crossreacts with the 400 kDa protein in the pia mater of dystrophin-deficient mdx mouse brainS Ishiura, K Arahata, T Tsukahara, et al.
Journal of the Neurological Sciences|December 1, 1995
Congenital hypomyelination neuropathy: decreased expression of the P2 protein in peripheral nerve with normal DNA sequence of the coding regionY Sawaishi, K Hayasaka, A Goto, et al.
Pageof 51