Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Satoru Noguchi

Showing results (71-80 of 170) with videos related to

Pageof 17
Sort By:
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 MiceAya Harada, Megumi Goto, Atsuya Kato, et al.
Brain & Development|March 9, 2019
Phenotype of a limb-girdle congenital myasthenic syndrome patient carrying a GFPT1 mutationChihiro 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 ApproachesKelly 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 moleculesTakuya Matsumoto, Yohsuke Kamada, Toyonari Sugimoto, et al.
Human Molecular Genetics|March 7, 2003
cDNA microarray analysis of individual Duchenne muscular dystrophy patientsSatoru 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 myopathyMay 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 dystrophyMasashi Ogasawara, Nobuyuki Eura, Aritoshi Iida, et al.
Neurology. Genetics|December 22, 2021
<i>TNNI1</i> Mutated in Autosomal Dominant Proximal ArthrogryposisYukako 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 MyopathiesRui Shimazaki, Satoru Noguchi, Hotake Takizawa, et al.
Muscle & Nerve|April 1, 2018
Quantification of lectin fluorescence in GNE myopathy muscle biopsiesPetcharat Leoyklang, Bradley Class, Satoru Noguchi, et al.
Pageof 17

Showing results (71-80 of 170) with videos related to

Sort By:
Pageof 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 MiceAya Harada, Megumi Goto, Atsuya Kato, et al.
Brain & Development|March 9, 2019
Phenotype of a limb-girdle congenital myasthenic syndrome patient carrying a GFPT1 mutationChihiro 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 ApproachesKelly 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 moleculesTakuya Matsumoto, Yohsuke Kamada, Toyonari Sugimoto, et al.
Human Molecular Genetics|March 7, 2003
cDNA microarray analysis of individual Duchenne muscular dystrophy patientsSatoru 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 myopathyMay 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 dystrophyMasashi Ogasawara, Nobuyuki Eura, Aritoshi Iida, et al.
Neurology. Genetics|December 22, 2021
<i>TNNI1</i> Mutated in Autosomal Dominant Proximal ArthrogryposisYukako 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 MyopathiesRui Shimazaki, Satoru Noguchi, Hotake Takizawa, et al.
Muscle & Nerve|April 1, 2018
Quantification of lectin fluorescence in GNE myopathy muscle biopsiesPetcharat Leoyklang, Bradley Class, Satoru Noguchi, et al.
Pageof 17