Motoi Kanagawa

Ehime University — Japan

Biochemistry, Genetics and Molecular Biology · Life Sciences

31h-index4.9kcitations152works0.42yr avg
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Research Topics

Muscle Physiology and Disorders(62), Ubiquitin and proteasome pathways(14), Sirtuins and Resveratrol in Medicine(13), Adipose Tissue and Metabolism(12), Genetic Neurodegenerative Diseases(9)

Publications152 total

TRPV2 in muscle satellite cells is crucial for skeletal muscle remodelling
Cell Death and Disease·2025Open Access
<i>CRPPA</i> exon 6–9 deletion as a founder mutation in Chinese patients with dystroglycanopathy
Pediatric Investigation·2025Open Access
Validation of the FVB/N-Tg(HSA* LR)20bCath mice of myotonic dystrophy using swallowing function assessment, histology, and immunofluorescence analysis
PLoS ONE·2025Open Access
Defective O-mannosyl glycan synthesis in dystroglycanopathies: pathogenesis and therapeutic frontiers
Journal of Human Genetics·2025· 2 cited
Regulation of MCCC1 expression by a Parkinson’s disease-associated intronic variant: implications for pathogenesis
Journal of Human Genetics·2025· 2 citedOpen Access
Memorial Letter to Dr. Tamao Endo
Trends in Glycoscience and Glycotechnology·2025Open Access
Memorial Letter to Dr. Tamao Endo
Trends in Glycoscience and Glycotechnology·2025Open Access
Founder Mutation-Based&amp;nbsp;ISPD Mouse Model Reveals Mitochondrial Dysfunction: From Clinical Discovery to Mechanistic Insights in Dystroglycanopathy
SSRN Electronic Journal·2025Open Access
29P Temporal requirement of dystroglycan glycosylation during brain development and rescue of cortical dysplasia via gene delivery in the fetal stage
Neuromuscular Disorders·2024
Endogenous reductase activities for the generation of ribitol-phosphate, a CDP-ribitol precursor, in mammals
The Journal of Biochemistry·2023· 7 cited
Chain-specificity of laminin α1-5 LG45 modules in the recognition of carbohydrate-linked receptors and intramolecular binding
Scientific Reports·2023· 3 citedOpen Access
Laminin α5_CD239_Spectrin is a candidate association that compensates the linkage between the basement membrane and cytoskeleton in skeletal muscle fibers
Matrix Biology Plus·2022· 7 citedOpen Access
CDP-ribitol prodrug treatment ameliorates ISPD-deficient muscular dystrophy mouse model
Nature Communications·2022· 23 citedOpen Access
Muscle Transcriptomics Shows Overexpression of Cadherin 1 in Inclusion Body Myositis
Annals of Neurology·2022· 15 citedOpen Access
Dystroglycanopathy: From Elucidation of Molecular and Pathological Mechanisms to Development of Treatment Methods
International Journal of Molecular Sciences·2021· 50 citedOpen Access
Advances in Pathophysiology of Dystroglycanopathies and Its Treatment Strategies
Trends in Glycoscience and Glycotechnology·2021
Advances in Pathophysiology of Dystroglycanopathies and Its Treatment Strategies
Trends in Glycoscience and Glycotechnology·2021
Involvement of Transient Receptor Potential Vanilloid Channel 2 in the Induction of Lubricin and Suppression of Ectopic Endochondral Ossification in Mouse Articular Cartilage
Arthritis & Rheumatology·2021· 32 cited
CCDC 2061730: Experimental Crystal Structure Determination
The Cambridge Structural Database·2021Open Access
Hearing impairment associated with dysmyelination of the peripheral cochlear nerve in muscular dystrophy caused by aberrant α-dystroglycan glycosylation
Proceedings for Annual Meeting of The Japanese Pharmacological Society·2021Open Access
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Frequent Co-authors

Tatsushi Toda(33), Kazuhiro Kobayashi(23), Tamao Endo(13), Kevin P. Campbell(11), Hiroshi Manya(11), Mamoru Mizuno(6), Daniel E. Michele(5), Jakob S. Satz(5), Stefan Kunz(5), Michael B. A. Oldstone(5), Atsushi Kuga(5), Shin’ichi Takeda(5), Yuki Katanosaka(5), Yuji Hara(4), Takako Yoshida‐Moriguchi(4), Rita Barresi(4), Keiko Akasaka‐Manya(4), Chih‐Chieh Yu(4), Keiji Naruse(4), Yuko Miyagoe‐Suzuki(4)