K
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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Journal ArticleDOI
Establishment of a pancreatic beta cell line that retains glucose-inducible insulin secretion: special reference to expression of glucose transporter isoforms
Junichi Miyazaki,Kimi Araki,Eiji Yamato,Hiroshi Ikegami,Tomoichiro Asano,Yoshikazu Shibasaki,Yoshitomo Oka,Ken Ichi Yamamura +7 more
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
Yuichi Oike,Akira Hata,Takayoshi Mamiya,Tadashi Kaname,Yukihiro Noda,Misao Suzuki,Hirofumi Yasue,Toshitaka Nabeshima,Kimi Araki,Ken Ichi Yamamura +9 more
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.
Daisuke Hashimoto,Masaki Ohmuraya,Masahiko Hirota,Akitsugu Yamamoto,Koichi Suyama,Satoshi Ida,Yuushi Okumura,Etsuhisa Takahashi,Hiroshi Kido,Kimi Araki,Hideo Baba,Noboru Mizushima,Ken Ichi Yamamura +12 more
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
Kimi Araki,Jun-ichi Miyazaki,Okio Hino,Naohiro Tomita,Osamu Chisaka,Kenichi Matsubara,Ken Ichi Yamamura +6 more
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
Yuichi Oike,Nobuyuki Takakura,Nobuyuki Takakura,Akira Hata,Akira Hata,Tadashi Kaname,Tadashi Kaname,Miwa Akizuki,Miwa Akizuki,Yuji Yamaguchi,Yuji Yamaguchi,Hirofumi Yasue,Hirofumi Yasue,Kimi Araki,Kimi Araki,Ken Ichi Yamamura,Ken Ichi Yamamura,Toshio Suda +17 more
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.