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Kunihiro Tsuchida

Researcher at Fujita Health University

Publications -  157
Citations -  11440

Kunihiro Tsuchida is an academic researcher from Fujita Health University. The author has contributed to research in topics: ACVR2B & Myostatin. The author has an hindex of 51, co-authored 144 publications receiving 10444 citations. Previous affiliations of Kunihiro Tsuchida include National Institute of Advanced Industrial Science and Technology & Kyoto University.

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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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Mesenchymal progenitors distinct from satellite cells contribute to ectopic fat cell formation in skeletal muscle.

TL;DR: It is suggested that interaction between muscle cells and PDGFRα+ mesenchymal progenitors, not the fate decision of satellite cells, has a considerable impact on muscle homeostasis and is the major contributor to ectopic fat cell formation in skeletal muscle.
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Fibrosis and adipogenesis originate from a common mesenchymal progenitor in skeletal muscle.

TL;DR: Clonal analyses show that PDGFRα+ cells also differentiate into collagen type-I-producing cells, indicating that mesenchymal progenitors are the main origin of not only fat accumulation but also fibrosis in skeletal muscle.
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Molecular characterization of a functional cDNA for rat substance P receptor.

TL;DR: The observed sequence similarity and divergence would contribute to the expression of similar but pharmacologically distinguishable activities of the two tachykinin receptors.
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Cloning and expression of a rat neuromedin K receptor cDNA.

TL;DR: The sequence comparison of the rat neuromedin K, substance P, and substance K receptors revealed that these receptors are highly conserved in the seven transmembrane domains and the cytoplasmic sides of the receptors.