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Shinsuke Takagawa

Researcher at Tokyo Medical and Dental University

Publications -  10
Citations -  757

Shinsuke Takagawa is an academic researcher from Tokyo Medical and Dental University. The author has contributed to research in topics: Bleomycin & Dermis. The author has an hindex of 8, co-authored 10 publications receiving 720 citations.

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Journal ArticleDOI

Animal model of sclerotic skin. I: Local injections of bleomycin induce sclerotic skin mimicking scleroderma

TL;DR: The results suggest that dermal sclerosis induced by BLM closely resembles systemic sclerosis both histologically and biochemically.
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Signal Transducer and Activator of Transcription 6 Is Essential in the Induction of Contact Hypersensitivity

TL;DR: The data suggest that the STAT6 signal plays a critical role in the induction phase of CHS, and adoptive transfer experiments revealed that STAT6−/− mice induced CHS after injection of lymph node cells obtained from sensitized wt mice.
Journal Article

Animal model of sclerotic skin. II. Bleomycin induced scleroderma in genetically mast cell deficient WBB6F1-W/W(V) mice.

TL;DR: Results show that mast cell is not necessary for inducing Dermal sclerosis by bleomycin, and other types of inflammatory cells such as infiltrating macrophages or T lymphocytes may play a role in triggering induction of dermal sclerosis via fibrogenic cytokines.
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Effect of superoxide dismutase on bleomycin-induced dermal sclerosis: implications for the treatment of systemic sclerosis.

TL;DR: Systemic PC-superoxide dismutase markedly inhibited the development of dermal sclerosis, which was also accompanied by a decrease in the number of infiltrating mast cells and eosinophils, which indicates that administration of superoxide dismUTase may be effective in the therapeutic approach in systemic sclerosis.
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Hepatocyte growth factor both prevents and ameliorates the symptoms of dermal sclerosis in a mouse model of scleroderma

TL;DR: HGF-gene transfection both prevented and ameliorated the symptoms of not only dermal sclerosis but also of lung fibrosis induced by a subcutaneous BLM injection, indicating that gene therapy by the transfections of the human HGF cDNA may be a useful therapy for SSc and lung fibritis involved with SSc.