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Mitsuhito Wada

Showing results (1-10 of 7) with videos related to

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Journal of Computational Chemistry|December 9, 2004
A quantum chemical method for rapid optimization of protein structuresMitsuhito Wada, Minoru Sakurai
Journal of Chemical Information and Modeling|August 19, 2011
Selection of in silico drug screening results for G-protein-coupled receptors by using universal active probesMitsuhito Wada, Eiji Kanamori, Haruki Nakamura, et al.
The Journal of Biological Chemistry|October 3, 2013
Structural basis for the different stability and activity between the Cdk5 complexes with p35 and p39 activatorsTaro Saito, Masashi Yano, Yusei Kawai, et al.
Protein Engineering, Design & Selection : PEDS|October 15, 2019
Free-energy landscape of molecular interactions between endothelin 1 and human endothelin type B receptor: fly-casting mechanismJunichi Higo, Kota Kasahara, Mitsuhito Wada, et al.
Scientific Reports|February 28, 2020
A<sub>2B</sub> adenosine receptor inhibition by the dihydropyridine calcium channel blocker nifedipine involves colonic fluid secretionTeita Asano, Yuto Noda, Ken-Ichiro Tanaka, et al.
Journal of Neurochemistry|March 31, 2007
Cdk5--p39 is a labile complex with the similar substrate specificity to Cdk5--p35Mari Yamada, Taro Saito, Yutaka Sato, et al.
Bioorganic & Medicinal Chemistry|May 22, 2014
Synthesis and biological comparison of enantiomers of mepenzolate bromide, a muscarinic receptor antagonist with bronchodilatory and anti-inflammatory activitiesYasunobu Yamashita, Ken-Ichiro Tanaka, Teita Asano, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Journal of Computational Chemistry|December 9, 2004
A quantum chemical method for rapid optimization of protein structuresMitsuhito Wada, Minoru Sakurai
Journal of Chemical Information and Modeling|August 19, 2011
Selection of in silico drug screening results for G-protein-coupled receptors by using universal active probesMitsuhito Wada, Eiji Kanamori, Haruki Nakamura, et al.
The Journal of Biological Chemistry|October 3, 2013
Structural basis for the different stability and activity between the Cdk5 complexes with p35 and p39 activatorsTaro Saito, Masashi Yano, Yusei Kawai, et al.
Protein Engineering, Design & Selection : PEDS|October 15, 2019
Free-energy landscape of molecular interactions between endothelin 1 and human endothelin type B receptor: fly-casting mechanismJunichi Higo, Kota Kasahara, Mitsuhito Wada, et al.
Scientific Reports|February 28, 2020
A<sub>2B</sub> adenosine receptor inhibition by the dihydropyridine calcium channel blocker nifedipine involves colonic fluid secretionTeita Asano, Yuto Noda, Ken-Ichiro Tanaka, et al.
Journal of Neurochemistry|March 31, 2007
Cdk5--p39 is a labile complex with the similar substrate specificity to Cdk5--p35Mari Yamada, Taro Saito, Yutaka Sato, et al.
Bioorganic & Medicinal Chemistry|May 22, 2014
Synthesis and biological comparison of enantiomers of mepenzolate bromide, a muscarinic receptor antagonist with bronchodilatory and anti-inflammatory activitiesYasunobu Yamashita, Ken-Ichiro Tanaka, Teita Asano, et al.
Pageof 1