Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Yoshiro Sohma"'
Autor:
Isik Turker, Chih-Chieh Yu, Po-Cheng Chang, Zhenhui Chen, Yoshiro Sohma, Shien-Fong Lin, Peng-Sheng Chen, Tomohiko Ai
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e70450 (2013)
Apamin sensitive potassium current (I KAS), carried by the type 2 small conductance Ca(2+)-activated potassium (SK2) channels, plays an important role in post-shock action potential duration (APD) shortening and recurrent spontaneous ventricular fibr
Externí odkaz:
https://doaj.org/article/29c32367984b478c96ca52a2dde98311
Autor:
Yuka Kozawa, Akiko Yamamoto, Miyuki Nakakuki, Kotoyo Fujiki, Shiho Kondo, Takuto Okada, Tomoya Fukuyasu, Makoto Yamaguchi, Itsuka Taniguchi, Nao Nomura, Libin Liu, Mayuko Higuchi, Erina Niwa, Yoshiro Sohma, Satoru Naruse, Yoshifumi Takeyama, Hiroshi Ishiguro
Publikováno v:
Journal of Human Genetics.
Publikováno v:
Proceedings for Annual Meeting of The Japanese Pharmacological Society. 96:1-B
Autor:
Takaharu Kondo, Shigeru B. H. Ko, Yoshiro Sohma, Hiroshi Ishiguro, Kieran Smallbone, Martin C. Steward, Makoto Yamaguchi, Akiko Yamamoto
Publikováno v:
The Journal of Physiology. 595:1947-1972
Key points The ductal system of the pancreas secretes large volumes of alkaline fluid containing HCO3- concentrations as high as 140 mm during hormonal stimulation. A computational model has been constructed to explore the underlying ion transport me
Publikováno v:
The Journal of General Physiology
Identification of the binding sites for small molecules that alleviate gating defects in CFTR would assist rational drug design for the treatment of cystic fibrosis. Yeh et al. identify two potential binding sites for prototypical CFTR potentiators a
Publikováno v:
The Journal of Physiology. 594:3227-3244
Key points Two functional abnormalities of cystic fibrosis transmembrane conductance regulator (CFTR), a 25% reduction of the single-channel conductance (g) and a ∼13-fold lower open probability (Po ), were found with the R117H mutation that is ass
Autor:
Ying-Chun Yu, Kanako Wakabayashi-Nakao, Hiroshi Ishiguro, Yoshiro Sohma, Miyuki Nakakuki, Tzyh Chang Hwang
Publikováno v:
The journal of physiological sciences : JPS. 69(1)
A massive deletion over three exons 16-17b in the CFTR gene was identified in Japanese CF patients with the highest frequency (about 70% of Japanese CF patients definitely diagnosed). This pathogenic mutation results in a deletion of 153 amino acids
Publikováno v:
Biophysics and Physicobiology
Cystic fibrosis transmembrane conductance regulator (CFTR) is an anion channel that belongs to the ATP binding cassette protein superfamily. Deletion of phenylalanine at position 508 (ΔF508) is the most common CF-associated mutation and is present i
Publikováno v:
Current opinion in pharmacology. 34
One major breakthrough in cystic fibrosis research in the past decade is the development of drugs that target the root cause of the disease — dysfunctional CFTR protein. One of the compounds, Ivacaftor or Kalydeco, which has been approved for clini
Autor:
Shuntaro Chiba, Tadaomi Furuta, Minoru Sakurai, Norio Yoshida, Tomoka Furukawa-Hagiya, Tomohiko Hayashi, Yoshiro Sohma
Publikováno v:
Chem. Phys. Lett.. :165-170
ATP binding cassette proteins shuttle a variety of molecules across cell membranes. The substrate transportation process is initiated by the ATP-driven dimerization of nucleotide binding domains (NBDs). Here, the integral-equation theory of liquids w