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Hidetoshi Sakurai

Showing results (61-70 of 101) with videos related to

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Development (Cambridge, England)|September 6, 2005
Characterization of mesendoderm: a diverging point of the definitive endoderm and mesoderm in embryonic stem cell differentiation cultureShinsuke Tada, Takumi Era, Chikara Furusawa, et al.
American Journal of Physiology. Cell Physiology|August 1, 2022
Dissociation of SH3 and cysteine-rich domain 3 and junctophilin 1 from dihydropyridine receptor in dystrophin-deficient musclesYuki Ashida, Koichi Himori, Nao Tokuda, et al.
Acta Neuropathologica Communications|March 6, 2026
Translation of expanded CGG repeats in LRP12 associated oculopharyngodistal myopathyChengcheng Li, Jil A Daw, Sara K Pittman, et al.
Plos One|November 2, 2012
In vitro modeling of paraxial mesodermal progenitors derived from induced pluripotent stem cellsHidetoshi Sakurai, Yasuko Sakaguchi, Emi Shoji, et al.
Stem Cell Research & Therapy|September 19, 2024
Cell transplantation-mediated dystrophin supplementation efficacy in Duchenne muscular dystrophy mouse motor function improvement demonstrated by enhanced skeletal muscle fatigue toleranceClémence Kiho Bourgeois Yoshioka, Nana Takenaka-Ninagawa, Megumi Goto, et al.
Stem Cells Translational Medicine|June 29, 2019
Phenotypic Drug Screening for Dysferlinopathy Using Patient-Derived Induced Pluripotent Stem CellsYuko Kokubu, Tomoko Nagino, Katsunori Sasa, et al.
Brain : a Journal of Neurology|July 29, 2025
Aberrant lysosomal dynamics disrupt myogenesis via mTORC1 signalling in X-linked myotubular myopathyKengo Kora, Takeshi Yoshida, Atsushi Yokoyama, et al.
Brain Communications|June 30, 2022
Cell type-specific abnormalities of central nervous system in myotonic dystrophy type 1Masayuki Nakamori, Hiroshi Shimizu, Kotaro Ogawa, et al.
Scientific Reports|August 21, 2015
Early pathogenesis of Duchenne muscular dystrophy modelled in patient-derived human induced pluripotent stem cellsEmi Shoji, Hidetoshi Sakurai, Tokiko Nishino, et al.
Biomedicines|March 29, 2023
Evaluation of Human-Induced Pluripotent Stem Cells Derived from a Patient with Schwartz-Jampel Syndrome Revealed Distinct Hyperexcitability in the Skeletal MusclesYuri Yamashita, Satoshi Nakada, Kyoko Nakamura, et al.
Pageof 11

Showing results (61-70 of 101) with videos related to

Sort By:
Pageof 11
Development (Cambridge, England)|September 6, 2005
Characterization of mesendoderm: a diverging point of the definitive endoderm and mesoderm in embryonic stem cell differentiation cultureShinsuke Tada, Takumi Era, Chikara Furusawa, et al.
American Journal of Physiology. Cell Physiology|August 1, 2022
Dissociation of SH3 and cysteine-rich domain 3 and junctophilin 1 from dihydropyridine receptor in dystrophin-deficient musclesYuki Ashida, Koichi Himori, Nao Tokuda, et al.
Acta Neuropathologica Communications|March 6, 2026
Translation of expanded CGG repeats in LRP12 associated oculopharyngodistal myopathyChengcheng Li, Jil A Daw, Sara K Pittman, et al.
Plos One|November 2, 2012
In vitro modeling of paraxial mesodermal progenitors derived from induced pluripotent stem cellsHidetoshi Sakurai, Yasuko Sakaguchi, Emi Shoji, et al.
Stem Cell Research & Therapy|September 19, 2024
Cell transplantation-mediated dystrophin supplementation efficacy in Duchenne muscular dystrophy mouse motor function improvement demonstrated by enhanced skeletal muscle fatigue toleranceClémence Kiho Bourgeois Yoshioka, Nana Takenaka-Ninagawa, Megumi Goto, et al.
Stem Cells Translational Medicine|June 29, 2019
Phenotypic Drug Screening for Dysferlinopathy Using Patient-Derived Induced Pluripotent Stem CellsYuko Kokubu, Tomoko Nagino, Katsunori Sasa, et al.
Brain : a Journal of Neurology|July 29, 2025
Aberrant lysosomal dynamics disrupt myogenesis via mTORC1 signalling in X-linked myotubular myopathyKengo Kora, Takeshi Yoshida, Atsushi Yokoyama, et al.
Brain Communications|June 30, 2022
Cell type-specific abnormalities of central nervous system in myotonic dystrophy type 1Masayuki Nakamori, Hiroshi Shimizu, Kotaro Ogawa, et al.
Scientific Reports|August 21, 2015
Early pathogenesis of Duchenne muscular dystrophy modelled in patient-derived human induced pluripotent stem cellsEmi Shoji, Hidetoshi Sakurai, Tokiko Nishino, et al.
Biomedicines|March 29, 2023
Evaluation of Human-Induced Pluripotent Stem Cells Derived from a Patient with Schwartz-Jampel Syndrome Revealed Distinct Hyperexcitability in the Skeletal MusclesYuri Yamashita, Satoshi Nakada, Kyoko Nakamura, et al.
Pageof 11