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CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainate.
Suzuki, Toshimitsu; Tatsukawa, Tetsuya; Sudo, Genki; Delandre, Caroline; Pai, Yun Jin; Miyamoto, Hiroyuki; Raveau, Matthieu; Shimohata, Atsushi; Ohmori, Iori; Hamano, Shin-Ichiro; Haginoya, Kazuhiro; Uematsu, Mitsugu; Takahashi, Yukitoshi; Morimoto, Masafumi; Fujimoto, Shinji; Osaka, Hitoshi; Oguni, Hirokazu; Osawa, Makiko; Ishii, Atsushi; Hirose, Shinichi; Kaneko, Sunao; Inoue, Yushi; Moore, Adrian Walton; Yamakawa, Kazuhiro.
Afiliación
  • Suzuki T; Department of Neurodevelopmental Disorder Genetics, Institute of Brain Science, Nagoya City University Graduate School of Medical Science, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya, Aichi, 467-8601, Japan.
  • Tatsukawa T; Laboratory for Neurogenetics, RIKEN Center for Brain Science, Saitama, Japan.
  • Sudo G; Laboratory for Neurogenetics, RIKEN Center for Brain Science, Saitama, Japan.
  • Delandre C; Laboratory for Neurogenetics, RIKEN Center for Brain Science, Saitama, Japan.
  • Pai YJ; Laboratory for Genetic Control of Neuronal Architecture, RIKEN Center for Brain Science, Saitama, Japan.
  • Miyamoto H; Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.
  • Raveau M; Laboratory for Genetic Control of Neuronal Architecture, RIKEN Center for Brain Science, Saitama, Japan.
  • Shimohata A; Laboratory for Neurogenetics, RIKEN Center for Brain Science, Saitama, Japan.
  • Ohmori I; Laboratory for Neurogenetics, RIKEN Center for Brain Science, Saitama, Japan.
  • Hamano SI; Laboratory for Neurogenetics, RIKEN Center for Brain Science, Saitama, Japan.
  • Haginoya K; Department of Physiology, Nippon Medical School, Tokyo, Japan.
  • Uematsu M; Department of Special Needs Education, Okayama University Graduate School of Education, Okayama, Japan.
  • Takahashi Y; Division of Neurology, Saitama Children's Medical Center, Saitama, Japan.
  • Morimoto M; Department of Pediatric Neurology, Miyagi Children's Hospital, Sendai, Japan.
  • Fujimoto S; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
  • Osaka H; Department of Pediatrics, Gifu Prefectural Gifu Hospital, Gifu, Japan.
  • Oguni H; National Epilepsy Center, NHO Shizuoka Institute of Epilepsy and Neurological Disorder, Shizuoka, Japan.
  • Osawa M; Department of Pediatrics, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Ishii A; Department of Pediatrics, Neonatology and Congenital Disorders, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Hirose S; Tsutsujigaoka Children's Clinic, Aichi, Japan.
  • Kaneko S; Department of Pediatrics, Jichi Medical University, Shimotsuke, Japan.
  • Inoue Y; Department of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan.
  • Moore AW; Department of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan.
  • Yamakawa K; Department of Pediatrics, School of Medicine and Research Institute for the Molecular Pathomechanisms of Epilepsy, Fukuoka University, Fukuoka, Japan.
Sci Rep ; 12(1): 6505, 2022 05 17.
Article en En | MEDLINE | ID: mdl-35581205
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Epilepsia / Epilepsia del Lóbulo Temporal Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Sci Rep Año: 2022 Tipo del documento: Article País de afiliación: Japón
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Epilepsia / Epilepsia del Lóbulo Temporal Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Sci Rep Año: 2022 Tipo del documento: Article País de afiliación: Japón