Motoi Kanagawa

Professor

Ehime University Graduate School of Medicine

Japan

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Professor Motoi Kanagawa is a faculty member at Ehime University Graduate School of Medicine in Japan. His research focuses on various aspects of muscle biology, including the molecular mechanisms of muscular dystrophies and the role of specific proteins in muscle function. Recent articles authored by Professor Kanagawa explore topics such as reductase activities in mammals, transcriptomics in inclusion body myositis, and the interactions between laminin and cytoskeletal elements.

Articles (12)

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2024

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2023

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2022

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2022

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2022

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2021

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2021

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2020

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2020

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2020

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2020

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2020

Collaborators (7)

Yuji Yamada

Tokyo University of Pharmacy and Life Sciences

JAPAN

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Keisuke Hamada

Tokyo University of Pharmacy and Life Sciences

JAPAN

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Kazuhiro Kobayashi

Associate Professor

Kobe University

JAPAN

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Takashi Okada

Director/Professor

University of Tokyo

JAPAN

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Tatsushi Toda

University of Tokyo

JAPAN

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Shushi Nagamori

Jikei University School of Medicine

JAPAN

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Chiseko Ikenaga

Assistant Professor

Kitasato University

JAPAN

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Motoi Kanagawa

Research Interests

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Articles (12)

Endogenous reductase activities for the generation of ribitol-phosphate, a CDP-ribitol precursor, in mammals.

Chain-specificity of laminin α1-5 LG45 modules in the recognition of carbohydrate-linked receptors and intramolecular binding.

CDP-ribitol prodrug treatment ameliorates ISPD-deficient muscular dystrophy mouse model

Laminin α5_CD239_Spectrin is a candidate association that compensates the linkage between the basement membrane and cytoskeleton in skeletal muscle fibers.

Muscle Transcriptomics Shows Overexpression of Cadherin 1 in Inclusion Body Myositis.

Dystroglycanopathy: From Elucidation of Molecular and Pathological Mechanisms to Development of Treatment Methods.

TRPV2 is involved in induction of lubricin and suppression of ectopic endochondral ossification in articular joints.

Angiotensin II and Amyloid-β Synergistically Induce Brain Vascular Smooth Muscle Cell Senescence.

Lactone-Driven Ester-to-Amide Derivatization for Sialic Acid Linkage-Specific Alkylamidation.

Congenital hearing impairment associated with peripheral cochlear nerve dysmyelination in glycosylation-deficient muscular dystrophy.

Galectin 3-binding protein suppresses amyloid-β production by modulating β-cleavage of amyloid precursor protein.

Crystal structures of fukutin-related protein (FKRP), a ribitol-phosphate transferase related to muscular dystrophy.

Collaborators (7)

Yuji Yamada

Keisuke Hamada

Kazuhiro Kobayashi

Takashi Okada

Tatsushi Toda

Shushi Nagamori

Chiseko Ikenaga

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