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Mamoru Ouchida

Showing results (11-20 of 97) with videos related to

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Brain & Development|August 9, 2003
Paroxysmal movement disorders in severe myoclonic epilepsy in infancyYoko Ohtsuka, Iori Ohmori, Tatsuya Ogino, et al.
Neurobiology of Disease|November 13, 2022
Thioredoxin deficiency increases oxidative stress and causes bilateral symmetrical degeneration in rat midbrainIori Ohmori, Mamoru Ouchida, Hirohiko Imai, et al.
Epilepsia|May 9, 2022
Novel animal model of combined generalized and focal epilepsyIori Ohmori, Mamoru Ouchida, Masakazu Shinohara, et al.
Frontiers in Immunology|October 26, 2023
"Input/output cytokines" in epidermal keratinocytes and the involvement in inflammatory skin diseasesShin Morizane, Tomoyuki Mukai, Ko Sunagawa, et al.
Proteomics|July 14, 2011
Identification of direct targets for the miR-17-92 cluster by proteomic analysisHirotaka Kanzaki, Sachio Ito, Hiroko Hanafusa, et al.
Epilepsy Research|August 28, 2012
High-frequency EEG oscillations in hyperthermia-induced seizures of Scn1a mutant ratsKatsuhiro Kobayashi, Iori Ohmori, Keiichiro Hayashi, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|June 12, 2026
A novel spontaneous rat model of chronic kidney disease with mitochondrial dysfunction driven by thioredoxin insufficiencyIori K Ohmori, Mamoru Ouchida, Yoshiko Hada, et al.
Plos One|September 7, 2012
Novel direct targets of miR-19a identified in breast cancer cells by a quantitative proteomic approachMamoru Ouchida, Hirotaka Kanzaki, Sachio Ito, et al.
Cancer Letters|January 28, 2004
Establishment and characterization of a biphasic synovial sarcoma cell line, SYO-1Akira Kawai, Noriko Naito, Aki Yoshida, et al.
Brain & Development|September 18, 2003
Is phenotype difference in severe myoclonic epilepsy in infancy related to SCN1A mutations?Iori Ohmori, Yoko Ohtsuka, Mamoru Ouchida, et al.
Pageof 10

Showing results (11-20 of 97) with videos related to

Sort By:
Pageof 10
Brain & Development|August 9, 2003
Paroxysmal movement disorders in severe myoclonic epilepsy in infancyYoko Ohtsuka, Iori Ohmori, Tatsuya Ogino, et al.
Neurobiology of Disease|November 13, 2022
Thioredoxin deficiency increases oxidative stress and causes bilateral symmetrical degeneration in rat midbrainIori Ohmori, Mamoru Ouchida, Hirohiko Imai, et al.
Epilepsia|May 9, 2022
Novel animal model of combined generalized and focal epilepsyIori Ohmori, Mamoru Ouchida, Masakazu Shinohara, et al.
Frontiers in Immunology|October 26, 2023
"Input/output cytokines" in epidermal keratinocytes and the involvement in inflammatory skin diseasesShin Morizane, Tomoyuki Mukai, Ko Sunagawa, et al.
Proteomics|July 14, 2011
Identification of direct targets for the miR-17-92 cluster by proteomic analysisHirotaka Kanzaki, Sachio Ito, Hiroko Hanafusa, et al.
Epilepsy Research|August 28, 2012
High-frequency EEG oscillations in hyperthermia-induced seizures of Scn1a mutant ratsKatsuhiro Kobayashi, Iori Ohmori, Keiichiro Hayashi, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|June 12, 2026
A novel spontaneous rat model of chronic kidney disease with mitochondrial dysfunction driven by thioredoxin insufficiencyIori K Ohmori, Mamoru Ouchida, Yoshiko Hada, et al.
Plos One|September 7, 2012
Novel direct targets of miR-19a identified in breast cancer cells by a quantitative proteomic approachMamoru Ouchida, Hirotaka Kanzaki, Sachio Ito, et al.
Cancer Letters|January 28, 2004
Establishment and characterization of a biphasic synovial sarcoma cell line, SYO-1Akira Kawai, Noriko Naito, Aki Yoshida, et al.
Brain & Development|September 18, 2003
Is phenotype difference in severe myoclonic epilepsy in infancy related to SCN1A mutations?Iori Ohmori, Yoko Ohtsuka, Mamoru Ouchida, et al.
Pageof 10