K
Koki Moriyoshi
Researcher at Kyoto University
Publications - 36
Citations - 4758
Koki Moriyoshi is an academic researcher from Kyoto University. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 16, co-authored 27 publications receiving 4663 citations.
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Journal ArticleDOI
Molecular cloning and characterization of the rat NMDA receptor
Koki Moriyoshi,Masayuki Masu,Takahiro Ishii,Ryuichi Shigemoto,Noboru Mizuno,Shigetada Nakanishi +5 more
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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Molecular characterization of the family of the N-methyl-D-aspartate receptor subunits.
Takako Ishii,Koki Moriyoshi,Hidemitsu Sugihara,Kazuhiro Sakurada,Hiroshi Kadotani,Mineto Yokoi,Chihiro Akazawa,Ryuichi Shigemoto,Nobuhiro Mizuno,Masayuki Masu +9 more
TL;DR: Northern blotting and in situ hybridization analyses revealed that the expressions of individual mRNAs for the NMDAR2 subunits overlap in some brain regions but are also specialized in many other regions.
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Structures and properties of seven isoforms of the NMDA receptor generated by alternative splicing.
TL;DR: 6 additional isoforms of the NMDA receptor generated via alternative splicing by molecular analysis of cDNA clones isolated from a rat forebrain cDNA library are reported, indicating that theNMDA receptor consists of heterogeneous molecules that differ in the extracellular sequence of the amino- and carboxyl-terminal regions.
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Persistent expression of helix‐loop‐helix factor HES‐1 prevents mammalian neural differentiation in the central nervous system.
Makoto Ishibashi,Koki Moriyoshi,Yoshiki Sasai,Kohei Shiota,Shigetada Nakanishi,Ryoichiro Kageyama +5 more
TL;DR: Results show that persistent expression of HES‐1 severely perturbs neuronal and glial differentiation in the developing mammalian central nervous system.
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Labeling Neural Cells Using Adenoviral Gene Transfer of Membrane-Targeted GFP
TL;DR: This method should be useful for studying the dynamic processes of cell migration and the development of neuronal connections, as well as for analyzing the function of exogenous genes introduced into cells using the adenovirus vector.