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Kimi Araki

Researcher at Kumamoto University

Publications -  197
Citations -  7476

Kimi Araki is an academic researcher from Kumamoto University. The author has contributed to research in topics: Gene & Mutant. The author has an hindex of 40, co-authored 182 publications receiving 6512 citations. Previous affiliations of Kimi Araki include Asahikawa Medical College & Gwangju Institute of Science and Technology.

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Establishment of a pancreatic beta cell line that retains glucose-inducible insulin secretion: special reference to expression of glucose transporter isoforms

TL;DR: The MIN6 cell line will be especially useful to analyze the molecular mechanisms by which beta cells regulate insulin secretion in response to extracellular glucose concentrations, and a possible role of GT isoforms in glucose sensing by beta cells is discussed.
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Truncated CBP Protein Leads to Classical Rubinstein—Taybi Syndrome Phenotypes in Mice: Implications for a Dominant-Negative Mechanism

TL;DR: CBP +/- mice would be an excellent model for the study of the role of CBP in development and memory storage mechanisms, and studies with step-through-type passive avoidance tests and with fear conditioning test showed that mice were deficient in long-term memory (LTM).
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Involvement of autophagy in trypsinogen activation within the pancreatic acinar cells.

TL;DR: It is found that cytoplasmic vacuoles induced in pancreatic acinar cells by experimental pancreatitis were autophagic in origin, as demonstrated by microtubule-associated protein 1 light chain 3 expression and electron microscopy experiments, and trypsinogen activation was greatly reduced in the absence of autophagy.
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Expression and replication of hepatitis B virus genome in transgenic mice

TL;DR: Results demonstrate that the HBV genome integrated into the mouse chromosome acted as a template for viral gene expression, allowing viral replication, and should be useful for detailed studies of the replication and expression of HBV and for pathological studies of hepatitis, including the development of hepatocellular carcinoma.
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Mice Homozygous for a Truncated Form of CREB-Binding Protein Exhibit Defects in Hematopoiesis and Vasculo-angiogenesis

TL;DR: It is demonstrated that CBP plays an essential role in hematopoiesis and vasculo-angiogenesis and the analyses demonstrate that these defects were partially rescued by the addition of VEGF to this culture.