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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 12, 2025
Substitutions of nucleotides at the 3' ends of COL6A1/2/3 exons induce exon skipping associated with collagen VI-related muscular dystrophies and therapeutic strategies
Seung-Ah Lee, Megumu Ogawa, Yoshihiko Saito, et al.
In Vivo (Athens, Greece)
|
October 31, 2023
UVC-Protective Activity of Lemongrass Among 12 Fat-soluble Herbal Extracts: Rapid Decay Due to Cytotoxicity
Yusei Otaka, Maki Izawa, Hiroshi Sakagami, et al.
Cell Reports
|
February 24, 2017
LSD1 Controls Timely MyoD Expression via MyoD Core Enhancer Transcription
Isabella Scionti, Shinichiro Hayashi, Sandrine Mouradian, et al.
Neurology
|
July 11, 2020
ADSSL1 myopathy is the most common nemaline myopathy in Japan with variable clinical features
Yoshihiko Saito, Atsuko Nishikawa, Aritoshi Iida, et al.
Circulation Research
|
July 28, 2007
Estrogen-mediated endothelial progenitor cell biology and kinetics for physiological postnatal vasculogenesis
Haruchika Masuda, Christoph Kalka, Tomono Takahashi, et al.
Brain : a Journal of Neurology
|
February 18, 2026
SNUPN variants cause spinocerebellar atrophy by disrupting global splicing in cerebellar Purkinje cells
Mariko Okubo, Megumu Ogawa, Nobuyuki Eura, et al.
Drug Discoveries & Therapeutics
|
February 27, 2023
Age distribution and disease severity of COVID-19 patients continued to change in a time-dependent manner from May 2021 to April 2022 in the regional core hospital in Japan
Futoshi Kawaura, Takuya Kishi, Tadashi Yamamoto, et al.
Scientific Reports
|
December 16, 2022
Multidimensional analyses of the pathomechanism caused by the non-catalytic GNE variant, c.620A>T, in patients with GNE myopathy
Wakako Yoshioka, Aritoshi Iida, Kyuto Sonehara, et al.
Acta Neuropathologica Communications
|
November 26, 2020
CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations
Masashi Ogasawara, Aritoshi Iida, Theerawat Kumutpongpanich, et al.
Annals of Neurology
|
June 4, 2019
COX6A2 variants cause a muscle-specific cytochrome c oxidase deficiency
Michio Inoue, Shumpei Uchino, Aritoshi Iida, et al.
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Showing results (111-120 of 131) with videos related to
Sort By:
Page
of 14
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 12, 2025
Substitutions of nucleotides at the 3' ends of COL6A1/2/3 exons induce exon skipping associated with collagen VI-related muscular dystrophies and therapeutic strategies
Seung-Ah Lee, Megumu Ogawa, Yoshihiko Saito, et al.
In Vivo (Athens, Greece)
|
October 31, 2023
UVC-Protective Activity of Lemongrass Among 12 Fat-soluble Herbal Extracts: Rapid Decay Due to Cytotoxicity
Yusei Otaka, Maki Izawa, Hiroshi Sakagami, et al.
Cell Reports
|
February 24, 2017
LSD1 Controls Timely MyoD Expression via MyoD Core Enhancer Transcription
Isabella Scionti, Shinichiro Hayashi, Sandrine Mouradian, et al.
Neurology
|
July 11, 2020
ADSSL1 myopathy is the most common nemaline myopathy in Japan with variable clinical features
Yoshihiko Saito, Atsuko Nishikawa, Aritoshi Iida, et al.
Circulation Research
|
July 28, 2007
Estrogen-mediated endothelial progenitor cell biology and kinetics for physiological postnatal vasculogenesis
Haruchika Masuda, Christoph Kalka, Tomono Takahashi, et al.
Brain : a Journal of Neurology
|
February 18, 2026
SNUPN variants cause spinocerebellar atrophy by disrupting global splicing in cerebellar Purkinje cells
Mariko Okubo, Megumu Ogawa, Nobuyuki Eura, et al.
Drug Discoveries & Therapeutics
|
February 27, 2023
Age distribution and disease severity of COVID-19 patients continued to change in a time-dependent manner from May 2021 to April 2022 in the regional core hospital in Japan
Futoshi Kawaura, Takuya Kishi, Tadashi Yamamoto, et al.
Scientific Reports
|
December 16, 2022
Multidimensional analyses of the pathomechanism caused by the non-catalytic GNE variant, c.620A>T, in patients with GNE myopathy
Wakako Yoshioka, Aritoshi Iida, Kyuto Sonehara, et al.
Acta Neuropathologica Communications
|
November 26, 2020
CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations
Masashi Ogasawara, Aritoshi Iida, Theerawat Kumutpongpanich, et al.
Annals of Neurology
|
June 4, 2019
COX6A2 variants cause a muscle-specific cytochrome c oxidase deficiency
Michio Inoue, Shumpei Uchino, Aritoshi Iida, et al.
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of 14