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Ryo Goitsuka

Researcher at Tokyo University of Science

Publications -  105
Citations -  3045

Ryo Goitsuka is an academic researcher from Tokyo University of Science. The author has contributed to research in topics: Gene & Complementary DNA. The author has an hindex of 27, co-authored 101 publications receiving 2853 citations. Previous affiliations of Ryo Goitsuka include National Presto Industries & Keio University.

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FcεRI-mediated mast cell degranulation requires calcium-independent microtubule-dependent translocation of granules to the plasma membrane

TL;DR: It is shown that FcɛRI stimulation triggers the formation of microtubules in a manner independent of calcium, and that the Fyn/Gab2/RhoA (but not Lyn/SLP-76) signaling pathway plays a critical role in the calcium-independent microtubule-dependent pathway.
Journal Article

BASH, a novel signaling molecule preferentially expressed in B cells of the bursa of Fabricius.

TL;DR: A novel gene preferentially expressed in bursal B cells, designated BASH, is suggested to be involved in BCR-mediated signal transduction and could play a critical role in B cell development in the bursa.
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Cell cycle arrest and apoptosis induced by Notch1 in B cells.

TL;DR: Notch1 signaling induces apoptosis of the B cells through Hairy1, and the G1 cell cycle arrest through other pathways, which may account for the recent observations indicating the selective inhibition of early B cell development in mice by Notch1.
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SMAD1 signaling is critical for initial commitment of germ cell lineage from mouse epiblast.

TL;DR: It is shown that the intracellular signaling molecule SMAD1, acting downstream of bone morphogenetic protein (BMP) receptors, is required for the commitment of germ cell lineage from epiblast in early mouse embryos.
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The B cell-restricted adaptor BASH is required for normal development and antigen receptor-mediated activation of B cells.

TL;DR: The BASH-deficient B cells scarcely proliferated or up-regulated B7-2 in response to BCR ligation and poorly proliferated upon CD40 ligation or lipopolysaccharide stimulation, which indicates that BASH is critical for preB cell receptor signaling inducing proliferation of large preB cells and the following differentiation, for peripheral B cell maturation, and for BCR signaling inducing activation/proliferation of B cells.