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Ikuko Kadohira
Researcher at Keio University
Publications - 12
Citations - 243
Ikuko Kadohira is an academic researcher from Keio University. The author has contributed to research in topics: Ventricular outflow tract & Interrupted aortic arch. The author has an hindex of 7, co-authored 12 publications receiving 215 citations.
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Journal ArticleDOI
Molecular mechanisms of how mercury inhibits water permeation through aquaporin-1: understanding by molecular dynamics simulation.
TL;DR: It is suggested that mercury disrupts the water pore of AQP1 through local conformational changes in the ar/R region.
Journal ArticleDOI
Beta cell dysfunction and its clinical significance in gestational diabetes
Yoshifumi Saisho,Kei Miyakoshi,Mamoru Tanaka,Akira Shimada,Satoru Ikenoue,Ikuko Kadohira,Yasunori Yoshimura,Hiroshi Itoh +7 more
TL;DR: The level of beta cell dysfunction in GDM was associated with the severity of glucose intolerance and total insulin dosage required and these findings underpin clinical significance of betacell dysfunction inGDM.
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Phosphorylation in the C-terminal domain of Aquaporin-4 is required for Golgi transition in primary cultured astrocytes.
Ikuko Kadohira,Yoichiro Abe,Mutsuo Nuriya,Kazumi Sano,Shoji Tsuji,Takeshi Arimitsu,Yasunori Yoshimura,Masato Yasui +7 more
TL;DR: Observations indicate that the C-terminal domain of AQP4 is constitutively phosphorylated at least in part by protein kinase CK2 and it is required for Golgi transition.
Journal ArticleDOI
Comparison of the right and left ventricular performance during the fetal development using velocity vector imaging
Seon Hye Kim,Kei Miyakoshi,Ikuko Kadohira,Mamoru Tanaka,Kazuhiro Minegishi,Tadashi Matsumoto,Yasunori Yoshimura +6 more
TL;DR: The findings suggest the RV predominance of longitudinal contraction and dilatation, compared to the LV in uncomplicated fetuses during the fetal development using velocity vector imaging (VVI).
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Expression and distribution of tight junction proteins in human amnion during late pregnancy.
TL;DR: The findings suggest that the human amniotic epithelium has TJs that disrupt during late pregnancy, which may be induced by several factors such as glucocorticoids present in the amniotics fluid during lateregnancy.