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Isao Hamaguchi

Researcher at Kumamoto University

Publications -  9
Citations -  881

Isao Hamaguchi is an academic researcher from Kumamoto University. The author has contributed to research in topics: Tyrosine kinase & Receptor tyrosine kinase. The author has an hindex of 9, co-authored 9 publications receiving 854 citations.

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Critical Role of the TIE2 Endothelial Cell Receptor in the Development of Definitive Hematopoiesis

TL;DR: In vitro study revealed that Adhesion of TIE2+ cells induced by Angiopoietin-1 enhanced the proliferation of hematopoietic progenitor cells and promoted the adhesion to fibronectin (FN) through integrins in Tie2-transfected cells and primary TIE1+ cells sorted from 9.5 d.p.c. P-Sp.
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Molecular Cloning and Characterization of Mouse TIE and TEK Receptor Tyrosine Kinase Genes and Their Expression in Hematopoietic Stem Cells

TL;DR: Characterization of two novel genes of their full-length cDNA sequences revealed that they were mouse homologues of the endothelial cell RTK genes, TIE and TEK, which shared a unique structural property of coexistent immunoglobulin-like domain, epidermal growth factor-like repeats, and fibronectin type III repeats in their extracellular domains.
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In vitro hematopoietic and endothelial cell development from cells expressing TEK receptor in murine aorta-gonad-mesonephros region.

TL;DR: This in vitro coculture system shows that the TEK+ fraction of primary AGM cells is a candidate for hemangioblasts, which can differentiate into both hematopoietic cells and endothelial cells.
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Tyro 3 Receptor Tyrosine Kinase and its Ligand, Gas6, Stimulate the Function of Osteoclasts

TL;DR: The findings in this study are the first to indicate a new biological activity of Gas6 and protein S as a direct regulator of osteoclastic function; they give an insight into the role of these vitamin K‐dependent ligands in bone resorption in vivo.
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Translocation of the Csk homologous kinase (Chk/Hyl) controls activity of CD36‐anchored Lyn tyrosine kinase in thrombin‐stimulated platelets

TL;DR: Results suggest that Chk, but not Csk, may function as a translocation‐controlled negative regulator of CD36‐anchored Lyn in thrombin‐induced platelet activation.