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Masayuki Masu

Researcher at University of Tsukuba

Publications -  68
Citations -  11123

Masayuki Masu is an academic researcher from University of Tsukuba. The author has contributed to research in topics: Heparan sulfate & Metabotropic glutamate receptor 1. The author has an hindex of 30, co-authored 67 publications receiving 10832 citations. Previous affiliations of Masayuki Masu include University of California, San Francisco & Kyoto University.

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Molecular cloning and characterization of the rat NMDA receptor

TL;DR: A complementary DNA encoding the rat NMDA receptor has been cloned and characterized and it has been found that this protein has a significant sequence similarity to the AMPA/kainate receptors.
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Sequence and expression of a metabotropic glutamate receptor

TL;DR: The complementary DNA of a metabotropic glutamate receptor coupled to inositol phosphate/Ca2+ signal transduction has been cloned and characterized and abundant expression of this messenger RNA is observed in neuronal cells in hippocampal dentate gyrus and CA2−3 and in Cerebellar Purkinje cells, suggesting the importance of this receptor in specific hippocampal and cerebellar functions.
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A Family of Metabotropic Glutamate Receptors

TL;DR: Three cDNA clones were isolated from a rat brain cDNA library by cross-hybridization with the cDNA for a metabotropic glutamate receptor to form a novel family of G protein-coupled receptors that differ in their signal transduction and expression patterns.
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Deleted in Colorectal Cancer (DCC) Encodes a Netrin Receptor

TL;DR: Results indicate that DCC is a receptor or a component of a receptor that mediates the effects of netrin-1 on commissural axons, and they complement genetic evidence for interactions between DCC and netrin homologs in C. elegans and Drosophila.
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Phenotype of mice lacking functional Deleted in colorectal cancer (Dcc) gene.

TL;DR: Inactivation of the murine Dcc gene caused defects in axonal projections that are similar to those observed in netrin-1-deficient mice but did not affect growth, differentiation, morphogenesis or tumorigenesis in mouse intestine, which is consistent with the hypothesis that DCC is a component of a receptor for netrin -1.