Zobrazeno 1 - 10 of 90 pro vyhledávání: '"Fumiaki Saito"'
1
Akademický článek
Antioxidants restore store‐operated Ca2+ entry in patient‐iPSC‐derived myotubes with tubular aggregate myopathy‐associated Ile484ArgfsX21 STIM1 mutation via upregulation of binding immunoglobulin protein
Autor: Fusako Sakai‐Takemura, Fumiaki Saito, Ken'ichiro Nogami, Yusuke Maruyama, Ahmed Elhussieny, Kiichiro Matsumura, Shin'ichi Takeda, Yoshitsugu Aoki, Yuko Miyagoe‐Suzuki
Publikováno v: FASEB BioAdvances, Vol 5, Iss 11, Pp 453-469 (2023)
Abstract Store‐operated Ca2+ entry (SOCE) is indispensable for intracellular Ca2+ homeostasis in skeletal muscle, and constitutive activation of SOCE causes tubular aggregate myopathy (TAM). To understand the pathogenesis of TAM, we induced pluripo
Externí odkaz: https://doaj.org/article/9ab6fb4209e344dcab30a52c6893f7f7
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2
Akademický článek
N-terminal domain on dystroglycan enables LARGE1 to extend matriglycan on α-dystroglycan and prevents muscular dystrophy
Autor: Hidehiko Okuma, Jeffrey M Hord, Ishita Chandel, David Venzke, Mary E Anderson, Ameya S Walimbe, Soumya Joseph, Zeita Gastel, Yuji Hara, Fumiaki Saito, Kiichiro Matsumura, Kevin P Campbell
Publikováno v: eLife, Vol 12 (2023)
Dystroglycan (DG) requires extensive post-translational processing and O-glycosylation to function as a receptor for extracellular matrix (ECM) proteins containing laminin-G (LG) domains. Matriglycan is an elongated polysaccharide of alternating xylo
Externí odkaz: https://doaj.org/article/61521eb8209340aeb031132b25b6d671
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3
Akademický článek
Unexpected Mutations by CRISPR-Cas9 CTG Repeat Excision in Myotonic Dystrophy and Use of CRISPR Interference as an Alternative Approach
Autor: Miki Ikeda, Mariko Taniguchi-Ikeda, Takema Kato, Yasuko Shinkai, Sonoko Tanaka, Hiroki Hagiwara, Naomichi Sasaki, Toshihiro Masaki, Kiichiro Matsumura, Masahiro Sonoo, Hiroki Kurahashi, Fumiaki Saito
Publikováno v: Molecular Therapy: Methods & Clinical Development, Vol 18, Iss , Pp 131-144 (2020)
Myotonic dystrophy type 1 is the most common type of adult-onset muscular dystrophy. This is an autosomal dominant disorder and caused by the expansion of the CTG repeat in the 3′ untranslated region of the dystrophia myotonica protein kinase (DMPK
Externí odkaz: https://doaj.org/article/023d7e99a665465ca9bfb584a02b1aa6
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4
Akademický článek
Inhibitory Action of Daunorubicin on Lipopolysaccharide-Stimulated Inducible-Type Nitric Oxide Synthase Induction in Alveolar Macrophages
Autor: Fumiaki Saito, Satoshi Matsusaka, Hirohisa Kato, Ichiro Wakabayashi
Publikováno v: Journal of Pharmacological Sciences, Vol 99, Iss 4, Pp 364-372 (2005)
The purpose of this study was to investigate the effects of daunorubicin on lipopolysaccharide (LPS)-stimulated inducible-type nitric oxide synthase (iNOS) expression in macrophages. LPS-stimulated iNOS expression and NO production were significantly
Externí odkaz: https://doaj.org/article/7305844a198d4f8d915ebc4d30b12696
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7
Dystroglycan N-terminal domain enables LARGE1 to extend matriglycan on α-dystroglycan and prevents muscular dystrophy
Autor: Hidehiko Okuma, Jeffrey M. Hord, Ishita Chandel, David Venzke, Mary E. Anderson, Ameya S. Walimbe, Soumya Joseph, Zeita Gastel, Yuji Hara, Fumiaki Saito, Kiichiro Matsumura, Kevin P. Campbell
Dystroglycan (DG) requires extensive post-translational processing to function as a receptor for extracellular matrix proteins containing laminin-G-like (LG) domains. Matriglycan is an elongated polysaccharide of alternating xylose and glucuronic aci
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6a8b2ec891899535cbf1213ae64111ef
https://doi.org/10.1101/2022.08.09.502851
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9
Step-bunching instability of growing interfaces between ice and supercooled water
Autor: Ken-ichiro Murata, Masahide Sato, Makio Uwaha, Fumiaki Saito, Ken Nagashima, Gen Sazaki
Publikováno v: Proceedings of the National Academy of Sciences. 119
金沢大学学術メディア創成センター
Ice-crystal growth in supercooled water is one of the most familiar examples of phase-transition dynamics, playing essential roles in various natural phenomena on Earth. Despite its fundamental im
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::593d5d23bef6172a1b27f5d8c528f51b
https://doi.org/10.1073/pnas.2115955119
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10
Unexpected Mutations by CRISPR-Cas9 CTG Repeat Excision in Myotonic Dystrophy and Use of CRISPR Interference as an Alternative Approach
Autor: Hiroki Kurahashi, Hiroki Hagiwara, Naomichi Sasaki, Sonoko Tanaka, Miki Ikeda, Yasuko Shinkai, Kiichiro Matsumura, Mariko Taniguchi-Ikeda, Fumiaki Saito, Toshihiro Masaki, Takema Kato, Masahiro Sonoo
Publikováno v: Molecular Therapy: Methods & Clinical Development, Vol 18, Iss, Pp 131-144 (2020)
Molecular Therapy. Methods & Clinical Development
Myotonic dystrophy type 1 is the most common type of adult-onset muscular dystrophy. This is an autosomal dominant disorder and caused by the expansion of the CTG repeat in the 3′ untranslated region of the dystrophia myotonica protein kinase (DMPK
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17ff861ea29bd6654ed113ca87049ee5
http://www.sciencedirect.com/science/article/pii/S232905012030111X
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