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Atsuo Fukuda

Showing results (111-120 of 125) with videos related to

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Psychopharmacology|August 12, 2011
Phosphodiesterase 4 inhibition enhances the dopamine D1 receptor/PKA/DARPP-32 signaling cascade in frontal cortexMahomi Kuroiwa, Gretchen L Snyder, Takahide Shuto, et al.
Journal of Neuroendocrinology|October 30, 2023
Dual action of serotonin on local excitatory and inhibitory neural circuits regulating the corticotropin-releasing factor neurons in the paraventricular nucleus of the hypothalamusTakayuki Sato, Takuma Sugaya, Ashraf Hossain Talukder, et al.
Science Signaling|October 17, 2019
Developmentally regulated KCC2 phosphorylation is essential for dynamic GABA-mediated inhibition and survivalMiho Watanabe, Jinwei Zhang, M Shahid Mansuri, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 27, 2004
Malfunction of respiratory-related neuronal activity in Na+, K+-ATPase alpha2 subunit-deficient mice is attributable to abnormal Cl- homeostasis in brainstem neuronsKeiko Ikeda, Hiroshi Onimaru, Junko Yamada, et al.
Scientific Reports|October 20, 2015
De novo KCNB1 mutations in infantile epilepsy inhibit repetitive neuronal firingHirotomo Saitsu, Tenpei Akita, Jun Tohyama, et al.
Frontiers in Cellular Neuroscience|September 14, 2012
Refuting the challenges of the developmental shift of polarity of GABA actions: GABA more exciting than ever!Yehezkel Ben-Ari, Melanie A Woodin, Evelyne Sernagor, et al.
American Journal of Human Genetics|February 4, 2018
Biallelic Variants in CNPY3, Encoding an Endoplasmic Reticulum Chaperone, Cause Early-Onset Epileptic EncephalopathyHiroki Mutoh, Mitsuhiro Kato, Tenpei Akita, et al.
Scientific Reports|July 21, 2016
Impaired neuronal KCC2 function by biallelic SLC12A5 mutations in migrating focal seizures and severe developmental delayHirotomo Saitsu, Miho Watanabe, Tenpei Akita, et al.
Nature Genetics|May 13, 2008
De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathyHirotomo Saitsu, Mitsuhiro Kato, Takeshi Mizuguchi, et al.
Molecular Brain|December 31, 2010
The physiological roles of vesicular GABA transporter during embryonic development: a study using knockout miceKenzi Saito, Toshikazu Kakizaki, Ryotaro Hayashi, et al.
Pageof 13

Showing results (111-120 of 125) with videos related to

Sort By:
Pageof 13
Psychopharmacology|August 12, 2011
Phosphodiesterase 4 inhibition enhances the dopamine D1 receptor/PKA/DARPP-32 signaling cascade in frontal cortexMahomi Kuroiwa, Gretchen L Snyder, Takahide Shuto, et al.
Journal of Neuroendocrinology|October 30, 2023
Dual action of serotonin on local excitatory and inhibitory neural circuits regulating the corticotropin-releasing factor neurons in the paraventricular nucleus of the hypothalamusTakayuki Sato, Takuma Sugaya, Ashraf Hossain Talukder, et al.
Science Signaling|October 17, 2019
Developmentally regulated KCC2 phosphorylation is essential for dynamic GABA-mediated inhibition and survivalMiho Watanabe, Jinwei Zhang, M Shahid Mansuri, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 27, 2004
Malfunction of respiratory-related neuronal activity in Na+, K+-ATPase alpha2 subunit-deficient mice is attributable to abnormal Cl- homeostasis in brainstem neuronsKeiko Ikeda, Hiroshi Onimaru, Junko Yamada, et al.
Scientific Reports|October 20, 2015
De novo KCNB1 mutations in infantile epilepsy inhibit repetitive neuronal firingHirotomo Saitsu, Tenpei Akita, Jun Tohyama, et al.
Frontiers in Cellular Neuroscience|September 14, 2012
Refuting the challenges of the developmental shift of polarity of GABA actions: GABA more exciting than ever!Yehezkel Ben-Ari, Melanie A Woodin, Evelyne Sernagor, et al.
American Journal of Human Genetics|February 4, 2018
Biallelic Variants in CNPY3, Encoding an Endoplasmic Reticulum Chaperone, Cause Early-Onset Epileptic EncephalopathyHiroki Mutoh, Mitsuhiro Kato, Tenpei Akita, et al.
Scientific Reports|July 21, 2016
Impaired neuronal KCC2 function by biallelic SLC12A5 mutations in migrating focal seizures and severe developmental delayHirotomo Saitsu, Miho Watanabe, Tenpei Akita, et al.
Nature Genetics|May 13, 2008
De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathyHirotomo Saitsu, Mitsuhiro Kato, Takeshi Mizuguchi, et al.
Molecular Brain|December 31, 2010
The physiological roles of vesicular GABA transporter during embryonic development: a study using knockout miceKenzi Saito, Toshikazu Kakizaki, Ryotaro Hayashi, et al.
Pageof 13