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Frontiers in Cell and Developmental Biology
|
December 10, 2021
Systemic Supplementation of Collagen VI by Neonatal Transplantation of iPSC-Derived MSCs Improves Histological Phenotype and Function of Col6-Deficient Model Mice
Aya Harada, Megumi Goto, Atsuya Kato, et al.
Brain & Development
|
March 9, 2019
Phenotype of a limb-girdle congenital myasthenic syndrome patient carrying a GFPT1 mutation
Chihiro Matsumoto, Madoka Mori-Yoshimura, Satoru Noguchi, et al.
Journal of Neuromuscular Diseases
|
September 13, 2021
Visualizing Muscle Sialic Acid Expression in the GNED207VTgGne-/- Cmah-/- Model of GNE Myopathy: A Comparison of Dietary and Gene Therapy Approaches
Kelly E Crowe, Deborah A Zygmunt, Kristin Heller, et al.
Inorganic Chemistry
|
August 20, 2003
Electrical conducting and magnetic properties of (ethylenedithiotetrathiafulvalenothioquinone-1,3-diselenolemethide)2.FeBr4 (GaBr4) crystals with two different interlayer arrangements of donor molecules
Takuya Matsumoto, Yohsuke Kamada, Toyonari Sugimoto, et al.
Human Molecular Genetics
|
March 7, 2003
cDNA microarray analysis of individual Duchenne muscular dystrophy patients
Satoru Noguchi, Toshifumi Tsukahara, Masako Fujita, et al.
The Journal of Biological Chemistry
|
December 14, 2011
Peracetylated N-acetylmannosamine, a synthetic sugar molecule, efficiently rescues muscle phenotype and biochemical defects in mouse model of sialic acid-deficient myopathy
May Christine V Malicdan, Satoru Noguchi, Tomoharu Tokutomi, et al.
Acta Neuropathologica Communications
|
December 8, 2022
Intranuclear inclusions in muscle biopsy can differentiate oculopharyngodistal myopathy and oculopharyngeal muscular dystrophy
Masashi Ogasawara, Nobuyuki Eura, Aritoshi Iida, et al.
Neurology. Genetics
|
December 22, 2021
<i>TNNI1</i> Mutated in Autosomal Dominant Proximal Arthrogryposis
Yukako Nishimori, Aritoshi Iida, Masashi Ogasawara, et al.
Annals of Clinical and Translational Neurology
|
November 19, 2025
Chronological and Spatial Distribution of Skeletal Muscle Fat Replacement in FHL1-Related Myopathies
Rui Shimazaki, Satoru Noguchi, Hotake Takizawa, et al.
Muscle & Nerve
|
April 1, 2018
Quantification of lectin fluorescence in GNE myopathy muscle biopsies
Petcharat Leoyklang, Bradley Class, Satoru Noguchi, et al.
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Search research articles
Search
Showing results (71-80 of 170) with videos related to
Sort By:
Page
of 17
Frontiers in Cell and Developmental Biology
|
December 10, 2021
Systemic Supplementation of Collagen VI by Neonatal Transplantation of iPSC-Derived MSCs Improves Histological Phenotype and Function of Col6-Deficient Model Mice
Aya Harada, Megumi Goto, Atsuya Kato, et al.
Brain & Development
|
March 9, 2019
Phenotype of a limb-girdle congenital myasthenic syndrome patient carrying a GFPT1 mutation
Chihiro Matsumoto, Madoka Mori-Yoshimura, Satoru Noguchi, et al.
Journal of Neuromuscular Diseases
|
September 13, 2021
Visualizing Muscle Sialic Acid Expression in the GNED207VTgGne-/- Cmah-/- Model of GNE Myopathy: A Comparison of Dietary and Gene Therapy Approaches
Kelly E Crowe, Deborah A Zygmunt, Kristin Heller, et al.
Inorganic Chemistry
|
August 20, 2003
Electrical conducting and magnetic properties of (ethylenedithiotetrathiafulvalenothioquinone-1,3-diselenolemethide)2.FeBr4 (GaBr4) crystals with two different interlayer arrangements of donor molecules
Takuya Matsumoto, Yohsuke Kamada, Toyonari Sugimoto, et al.
Human Molecular Genetics
|
March 7, 2003
cDNA microarray analysis of individual Duchenne muscular dystrophy patients
Satoru Noguchi, Toshifumi Tsukahara, Masako Fujita, et al.
The Journal of Biological Chemistry
|
December 14, 2011
Peracetylated N-acetylmannosamine, a synthetic sugar molecule, efficiently rescues muscle phenotype and biochemical defects in mouse model of sialic acid-deficient myopathy
May Christine V Malicdan, Satoru Noguchi, Tomoharu Tokutomi, et al.
Acta Neuropathologica Communications
|
December 8, 2022
Intranuclear inclusions in muscle biopsy can differentiate oculopharyngodistal myopathy and oculopharyngeal muscular dystrophy
Masashi Ogasawara, Nobuyuki Eura, Aritoshi Iida, et al.
Neurology. Genetics
|
December 22, 2021
<i>TNNI1</i> Mutated in Autosomal Dominant Proximal Arthrogryposis
Yukako Nishimori, Aritoshi Iida, Masashi Ogasawara, et al.
Annals of Clinical and Translational Neurology
|
November 19, 2025
Chronological and Spatial Distribution of Skeletal Muscle Fat Replacement in FHL1-Related Myopathies
Rui Shimazaki, Satoru Noguchi, Hotake Takizawa, et al.
Muscle & Nerve
|
April 1, 2018
Quantification of lectin fluorescence in GNE myopathy muscle biopsies
Petcharat Leoyklang, Bradley Class, Satoru Noguchi, et al.
Page
of 17