Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tomoya Watanabe"'
Autor:
Asami Akita, Yasushi Ototake, Tomoya Watanabe, Noriko Komitsu, Tomohiko Tamura, Yukie Yamaguchi, Michiko Aihara, Daisuke Kurotaki, Miho Asami, Miwa Kanaoka
Publikováno v:
Journal of Investigative Dermatology. 141:1954-1963
Monocytes and macrophages may be involved in the pathogenesis of systemic sclerosis (SSc); however, the etiology and regulation of monocyte and macrophage function in SSc remain unknown. IRF8 is a transcriptional regulator that is essential for the d
Autor:
Tomoya Watanabe, Yasuhiro Nanri, Kenji Izuhara, Satoshi Nunomura, Shoichiro Ohta, Yukie Yamaguchi
Publikováno v:
Journal of Dermatological Science. 104:210-212
Autor:
Jonathan Heywood, Logan Mlakar, Carol Feghali-Bostwick, DeAnna Baker Frost, Tomoya Watanabe, Willian A. da Silveira, Gary Hardiman
Publikováno v:
Genes
Volume 10
Issue 2
Genes, Vol 10, Iss 2, p 75 (2019)
Watanabe, T, Baker Frost, D, Mlakar, L, Heywood, J, da Silveira, W A, Hardiman, G & Feghali-Bostwick, C 2019, ' A Human Skin Model Recapitulates Systemic Sclerosis Dermal Fibrosis and Identifies COL22A1 as a TGFβ Early Response Gene that Mediates Fibroblast to Myofibroblast Transition ', Genes, vol. 10, no. 2 . https://doi.org/10.3390/genes10020075
Volume 10
Issue 2
Genes, Vol 10, Iss 2, p 75 (2019)
Watanabe, T, Baker Frost, D, Mlakar, L, Heywood, J, da Silveira, W A, Hardiman, G & Feghali-Bostwick, C 2019, ' A Human Skin Model Recapitulates Systemic Sclerosis Dermal Fibrosis and Identifies COL22A1 as a TGFβ Early Response Gene that Mediates Fibroblast to Myofibroblast Transition ', Genes, vol. 10, no. 2 . https://doi.org/10.3390/genes10020075
Systemic sclerosis (SSc) is a complex multi-system autoimmune disease characterized by immune dysregulation, vasculopathy, and organ fibrosis. Skin fibrosis causes high morbidity and impaired quality of life in affected individuals. Animal models do
Autor:
Logan Mlakar, Tomoya Watanabe, Tetsuya Nishimoto, Jonathan Heywood, Stanley Hoffman, Maya Malaab, Carol Feghali-Bostwick
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 6, p e0179917 (2017)
PLoS ONE, Vol 12, Iss 6, p e0179917 (2017)
The murine bleomycin (BLM)-induced fibrosis model is the most widely used in systemic sclerosis (SSc) studies. It has been reported that systemic delivery of BLM via continuous diffusion from subcutaneously implanted osmotic minipumps can cause fibro