N
Naoya Asai
Researcher at Nagoya University
Publications - 113
Citations - 7955
Naoya Asai is an academic researcher from Nagoya University. The author has contributed to research in topics: Glial cell line-derived neurotrophic factor & Phosphorylation. The author has an hindex of 45, co-authored 109 publications receiving 7318 citations. Previous affiliations of Naoya Asai include Columbia University & Fujita Health University.
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Journal ArticleDOI
Characterization of a multicomponent receptor for GDNF
James J.S. Treanor,Laurie J. Goodman,Frederic J. de Sauvage,Donna M. Stone,Kristian Todd Poulsen,Claus D. Beck,Christa L. Gray,Mark Armanini,Richard A. Pollock,Franz Hefti,Heidi S. Phillips,Audry Goddard,Mark W. Moore,Anna Buj-Bello,Alun M. Davies,Naoya Asai,Masahide Takahashi,Richard Vandlen,Christopher E. Henderson,Arnon Rosenthal +19 more
TL;DR: It is demonstrated that physiological responses to GDNF require the presence of a novel glycosyl-phosphatidylinositol (GPI)-linked protein (designated GDNFR-α) that is expressed on GDNF-responsive cells and binds GDNF with a high affinity, which supports the hypothesis that GDNF uses a multi-subunit receptor system in which GDN FR-α and Ret function as the ligand-binding and signalling components.
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A GPI-linked Protein That Interacts With Ret to Form a Candidate Neurturin Receptor
Robert D. Klein,Robert D. Klein,Daniel Eric Sherman,Wei-Hsien Ho,Donna M. Stone,Gregory L. Bennett,Barbara Moffat,Richard Vandlen,Laura C. Simmons,Qimin Gu,Jo-Anne Hongo,Brigitte Devaux,Kristian Todd Poulsen,Mark Armanini,Chika Nozaki,Naoya Asai,Audrey Goddard,Heidi S. Phillips,Chris E. Henderson,Masahide Takahashi,Arnon Rosenthal +20 more
TL;DR: These findings identify Ret and NTNR-α as signalling and ligand-binding components, respectively, of a receptor for NTN and define a novel family of receptors for neurotrophic and differentiation factors composed of a shared transmembrane protein tyrosine kinase and a lig and-specific GPI-linked protein.
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Akt/PKB Regulates Actin Organization and Cell Motility via Girdin/APE
Atsushi Enomoto,Hideki Murakami,Naoya Asai,Nobuhiro Morone,Takashi Watanabe,Kumi Kawai,Yoshiki Murakumo,Jiro Usukura,Kozo Kaibuchi,Masahide Takahashi +9 more
TL;DR: This work identifies an Akt substrate, designated Girdin/APE (Akt-phosphorylation enhancer), which is an actin binding protein, which plays a crucial role in the formation of stress fibers and lamellipodia.
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Mechanism of activation of the ret proto-oncogene by multiple endocrine neoplasia 2a mutations
TL;DR: This result demonstrated that transport of the Ret protein to the plasma membrane is required for its transforming activity, and indicated that MEN 2A mutations induced ligand-independent dimerization of the c-Ret protein on the cell surface, leading to activation of its intrinsic tyrosine kinase.
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Etv4 and Etv5 are required downstream of GDNF and Ret for kidney branching morphogenesis.
Benson Lu,Cristina Cebrian,Xuan Chi,Satu Kuure,Richard Kuo,Carlton M. Bates,Silvia Arber,John A. Hassell,Lesley T. MacNeil,Masato Hoshi,Sanjay Jain,Naoya Asai,Masahide Takahashi,Kai M. Schmidt-Ott,Jonathan Barasch,Vivette D. D'Agati,Frank Costantini +16 more
TL;DR: Etv4 and Etv5 are key components of a gene network downstream of Ret that promotes and controls renal branching morphogenesis, and several genes whose expression in the ureteric bud depends on them are identified.