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Itaru Toyoshima

Showing results (41-50 of 43) with videos related to

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Rheumatology (Oxford, England)|December 5, 2013
A nationwide survey of Aicardi-Goutières syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort studyJunya Abe, Kazuyuki Nakamura, Ryuta Nishikomori, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 2011
Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndromeKazuhiko Arima, Akira Kinoshita, Hiroyuki Mishima, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 8, 2006
The role of G-protein-coupled receptor kinase 5 in pathogenesis of sporadic Parkinson's diseaseShigeki Arawaka, Manabu Wada, Saori Goto, et al.
Pageof 5

Showing results (41-50 of 43) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 43 results.
Rheumatology (Oxford, England)|December 5, 2013
A nationwide survey of Aicardi-Goutières syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort studyJunya Abe, Kazuyuki Nakamura, Ryuta Nishikomori, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 2011
Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndromeKazuhiko Arima, Akira Kinoshita, Hiroyuki Mishima, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 8, 2006
The role of G-protein-coupled receptor kinase 5 in pathogenesis of sporadic Parkinson's diseaseShigeki Arawaka, Manabu Wada, Saori Goto, et al.
Pageof 5