M
Masahiro Yamamoto
Researcher at Osaka University
Publications - 472
Citations - 36678
Masahiro Yamamoto is an academic researcher from Osaka University. The author has contributed to research in topics: Innate immune system & Immune system. The author has an hindex of 77, co-authored 434 publications receiving 33443 citations. Previous affiliations of Masahiro Yamamoto include Tokyo Medical and Dental University & National Institute of Radiological Sciences.
Papers
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Journal ArticleDOI
TRAF6 is required for generation of the B-1a B cell compartment as well as T cell-dependent and -independent humoral immune responses.
Takashi Kobayashi,Taesoo Kim,Anand Jacob,Matthew C. Walsh,Yuho Kadono,Ezequiel M. Fuentes-Pananá,Tomoko Yoshioka,Akihiko Yoshimura,Masahiro Yamamoto,Tsuneyasu Kaisho,Shizuo Akira,John G. Monroe,Yongwon Choi +12 more
TL;DR: Critical roles for TRAF6 are revealed in TD and TI humoral immune responses and in inductive fate decisions necessary to generate the B-1 B cell compartment in B cell progenitors.
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Single nucleotide polymorphism of TAG-1 influences IVIg responsiveness of Japanese patients with CIDP
Masahiro Iijima,Minoru Tomita,Saori Morozumi,Yuichi Kawagashira,Tomohiko Nakamura,Haruki Koike,Masahisa Katsuno,Nobutaka Hattori,Fumiaki Tanaka,Masahiro Yamamoto,Gen Sobue +10 more
TL;DR: Transient axonal glycoprotein 1 is a crucial molecule involved in IV immunoglobulin responsiveness in Japanese patients with chronic inflammatory demyelinating polyneuropathy, and is associated with single nucleotide polymorphisms and haplotype studies between IVIg responders and nonresponders.
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Functional and possible physical association of scavenger receptor with cytoplasmic tyrosine kinase Lyn in monocytic THP-1-derived macrophages
Shunji Miki,Satoshi Tsukada,Yu Nakamura,Saburo Aimoto,Hironobu Hojo,Bunzo Sato,Masahiro Yamamoto,Y Miki +7 more
TL;DR: Observations suggest a functional and possible physical association of SR‐A with Lyn in THP‐1‐derived macrophages, and also imply a possible involvement of Lyn inSR‐A signal transduction.
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Control of adipose tissue inflammation through TRB1.
Anke Ostertag,Allan Jones,Adam J. Rose,Maria Liebert,Stefan Kleinsorg,Anja Reimann,Alexandros Vegiopoulos,Mauricio Berriel Diaz,Daniela Strzoda,Masahiro Yamamoto,Takashi Satoh,Shizuo Akira,Stephan Herzig +12 more
TL;DR: Test the hypothesis that the TRB gene family fulfills broader functions in the integration of metabolic and inflammatory pathways in various tissues found that the expression of TRB1 was specifically upregulated during acute and chronic inflammation in WAT of mice.
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Possible involvement of suppression of Th2 differentiation in the anti-allergic effect of Sho-seiryu-to in mice.
TL;DR: In this paper, the Kampo medicine Sho-seiryu-to (SST) has been used in a double-blind randomized study of allergic asthma and rhinitis.