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Ikuya Nonaka

Showing results (101-110 of 169) with videos related to

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Neuromuscular Disorders : NMD|December 17, 2008
Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1BYoung-Eun Park, Yukiko K Hayashi, Kanako Goto, et al.
Molecular Genetics & Genomic Medicine|March 19, 2019
Three novel MTM1 pathogenic variants identified in Japanese patients with X-linked myotubular myopathyAtsuko Nishikawa, Aritoshi Iida, Shinichiro Hayashi, et al.
Experimental Animals|June 17, 2003
Canine X-linked muscular dystrophy in Japan (CXMDJ)Yoshiki Shimatsu, Kouichi Katagiri, Toshio Furuta, et al.
Neuromuscular Disorders : NMD|July 29, 2008
Distal lipid storage myopathy due to PNPLA2 mutationAya Ohkuma, Ikuya Nonaka, May Christine V Malicdan, et al.
Neuromuscular Disorders : NMD|July 28, 2016
Japanese multiple epidermal growth factor 10 (MEGF10) myopathy with novel mutations: A phenotype-genotype correlationKazuko Takayama, Satomi Mitsuhashi, Je-Young Shin, et al.
Annals of Neurology|January 4, 2011
Reversible infantile respiratory chain deficiency: a clinical and molecular studyMasakazu Mimaki, Hideyuki Hatakeyama, Hirofumi Komaki, et al.
Brain : a Journal of Neurology|July 27, 2014
Sialyllactose ameliorates myopathic phenotypes in symptomatic GNE myopathy model miceTakahiro Yonekawa, May Christine V Malicdan, Anna Cho, et al.
Developmental Biology|October 25, 2011
Filamin C plays an essential role in the maintenance of the structural integrity of cardiac and skeletal muscles, revealed by the medaka mutant zacroMisato Fujita, Hiroaki Mitsuhashi, Sumio Isogai, et al.
Mechanisms of Development|January 1, 2008
Osteogenic properties of human myogenic progenitor cellsNaohiro Hashimoto, Tohru Kiyono, Michiko R Wada, et al.
Neuromuscular Disorders : NMD|December 4, 2001
A point mutation of mitochondrial ATPase 6 gene in Leigh syndromeMotohiro Akagi, Koji Inui, Hiroko Tsukamoto, et al.
Pageof 17

Showing results (101-110 of 169) with videos related to

Sort By:
Pageof 17
Neuromuscular Disorders : NMD|December 17, 2008
Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1BYoung-Eun Park, Yukiko K Hayashi, Kanako Goto, et al.
Molecular Genetics & Genomic Medicine|March 19, 2019
Three novel MTM1 pathogenic variants identified in Japanese patients with X-linked myotubular myopathyAtsuko Nishikawa, Aritoshi Iida, Shinichiro Hayashi, et al.
Experimental Animals|June 17, 2003
Canine X-linked muscular dystrophy in Japan (CXMDJ)Yoshiki Shimatsu, Kouichi Katagiri, Toshio Furuta, et al.
Neuromuscular Disorders : NMD|July 29, 2008
Distal lipid storage myopathy due to PNPLA2 mutationAya Ohkuma, Ikuya Nonaka, May Christine V Malicdan, et al.
Neuromuscular Disorders : NMD|July 28, 2016
Japanese multiple epidermal growth factor 10 (MEGF10) myopathy with novel mutations: A phenotype-genotype correlationKazuko Takayama, Satomi Mitsuhashi, Je-Young Shin, et al.
Annals of Neurology|January 4, 2011
Reversible infantile respiratory chain deficiency: a clinical and molecular studyMasakazu Mimaki, Hideyuki Hatakeyama, Hirofumi Komaki, et al.
Brain : a Journal of Neurology|July 27, 2014
Sialyllactose ameliorates myopathic phenotypes in symptomatic GNE myopathy model miceTakahiro Yonekawa, May Christine V Malicdan, Anna Cho, et al.
Developmental Biology|October 25, 2011
Filamin C plays an essential role in the maintenance of the structural integrity of cardiac and skeletal muscles, revealed by the medaka mutant zacroMisato Fujita, Hiroaki Mitsuhashi, Sumio Isogai, et al.
Mechanisms of Development|January 1, 2008
Osteogenic properties of human myogenic progenitor cellsNaohiro Hashimoto, Tohru Kiyono, Michiko R Wada, et al.
Neuromuscular Disorders : NMD|December 4, 2001
A point mutation of mitochondrial ATPase 6 gene in Leigh syndromeMotohiro Akagi, Koji Inui, Hiroko Tsukamoto, et al.
Pageof 17