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Hideto Yonekura

Researcher at Tohoku University

Publications -  33
Citations -  2966

Hideto Yonekura is an academic researcher from Tohoku University. The author has contributed to research in topics: Gene & Complementary DNA. The author has an hindex of 24, co-authored 33 publications receiving 2887 citations.

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Cyclic ADP-ribose in insulin secretion from pancreatic beta cells

TL;DR: Results suggest that cADP-ribose is a mediator of calcium release from islet microsomes and may be generated in islets by glucose stimulation, serving as a second messenger for calcium mobilization in the endoplasmic reticulum.
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Synthesis and hydrolysis of cyclic ADP-ribose by human leukocyte antigen CD38 and inhibition of the hydrolysis by ATP.

TL;DR: A role for CD38 is indicated in the synthesis and hydrolysis of cADPR in the process of insulin secretion in pancreatic beta-cells, and it is found that ATP (2-10 mM), generated in the glucose metabolism in beta- cells, inhibited the cAD PR-hydrolyzing activity, resulting in the increased formation of c ADPR.
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Pancreatic beta-cell replication and amelioration of surgical diabetes by Reg protein

TL;DR: Results indicate that Reg protein is a growth factor for pancreatic beta cells and suggest that the administration of Reg protein could be used as another therapeutic approach for diabetes mellitus.
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Complete nucleotide sequence of human reg gene and its expression in normal and tumoral tissues. The reg protein, pancreatic stone protein, and pancreatic thread protein are one and the same product of the gene.

TL;DR: The human reg gene is isolated, determined its complete nucleotide sequence, and examined its expression in human tissues, indicating that the reg protein, pancreatic stone protein, and pancreatic thread protein are simply different names for a single protein deriving from the reg gene.
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Cyclic ADP-ribose Binds to FK506-binding Protein 12.6 to Release Ca2+ from Islet Microsomes

TL;DR: FK506, an immunosuppressant that prolongs allograft survival, as well as cADPR were found to induce the release of Ca2+ from islet microsomes, which strongly suggest that c ADPR may be the ligand for FKBP12.6 in islet RyR and that the binding of cAD PR to FK BP 12.6 frees the RyR from FKBA 12.