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Satoru Noguchi

Showing results (101-110 of 170) with videos related to

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Neuromuscular Disorders : NMD|March 25, 2014
GNE myopathy: a prospective natural history study of disease progressionMadoka Mori-Yoshimura, Yasushi Oya, Hiroyuki Yajima, et al.
Skeletal Muscle|September 1, 2015
Congenital muscular dystrophy with fatty liver and infantile-onset cataract caused by TRAPPC11 mutations: broadening of the phenotypeWen-Chen Liang, Wenhua Zhu, Satomi Mitsuhashi, 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.
Neuromuscular Disorders : NMD|April 2, 2014
GNE myopathy: new name and new mutation nomenclatureMarjan Huizing, Nuria Carrillo-Carrasco, May Christine V Malicdan, et al.
BMC Anesthesiology|March 25, 2026
Evaluation of clinically relevant sevoflurane concentrations in the development of malignant hyperthermia in an Ryr1 mutant mouse modelKenshiro Kido, Hirotsugu Miyoshi, Tsuyoshi Ikeda, 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 21, 2020
Two Japanese LGMDR25 patients with a biallelic recurrent nonsense variant of BVESLuh Ari Indrawati, Aritoshi Iida, Yuzo Tanaka, 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.
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.
Scientific Reports|February 22, 2018
Small-Vessel Vasculopathy Due to Aberrant Autophagy in LAMP-2 DeficiencyHuan T Nguyen, Satoru Noguchi, Kazuma Sugie, et al.
Pageof 17

Showing results (101-110 of 170) with videos related to

Sort By:
Pageof 17
Neuromuscular Disorders : NMD|March 25, 2014
GNE myopathy: a prospective natural history study of disease progressionMadoka Mori-Yoshimura, Yasushi Oya, Hiroyuki Yajima, et al.
Skeletal Muscle|September 1, 2015
Congenital muscular dystrophy with fatty liver and infantile-onset cataract caused by TRAPPC11 mutations: broadening of the phenotypeWen-Chen Liang, Wenhua Zhu, Satomi Mitsuhashi, 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.
Neuromuscular Disorders : NMD|April 2, 2014
GNE myopathy: new name and new mutation nomenclatureMarjan Huizing, Nuria Carrillo-Carrasco, May Christine V Malicdan, et al.
BMC Anesthesiology|March 25, 2026
Evaluation of clinically relevant sevoflurane concentrations in the development of malignant hyperthermia in an Ryr1 mutant mouse modelKenshiro Kido, Hirotsugu Miyoshi, Tsuyoshi Ikeda, 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 21, 2020
Two Japanese LGMDR25 patients with a biallelic recurrent nonsense variant of BVESLuh Ari Indrawati, Aritoshi Iida, Yuzo Tanaka, 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.
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.
Scientific Reports|February 22, 2018
Small-Vessel Vasculopathy Due to Aberrant Autophagy in LAMP-2 DeficiencyHuan T Nguyen, Satoru Noguchi, Kazuma Sugie, et al.
Pageof 17