Ohmori Iori 大守伊織

… Alternative Names

大守伊織オオモリイオリ

OOMORI Iori 大守伊織

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Researcher Number	20403488
Other IDs
Affiliation (Current)	2025: 岡山大学, 教育学域, 教授 2025: 京都大学, 医学研究科, 特定准教授
Affiliation (based on the past Project Information) *help	2022: 岡山大学, 教育学域, 教授 2016 – 2019: 岡山大学, 教育学研究科, 教授 2015: 岡山大学, 教育学研究科(研究院), 准教授 2014: 京都大学, 医学(系)研究科(研究院), 准教授 2011 – 2012: 岡山大学, 医歯(薬)学総合研究科, 助教 … More 2007 – 2012: Okayama University, 大学院・医歯薬学総合研究科, 助教 2006: 岡山大学, 大学・医歯薬学総合研究科, 助手 2005 – 2006: 岡山大学, 大学院・医歯薬学総合研究科, 助手 2005 – 2006: 岡山大学, 大学院医歯薬学総合研究科, 助手 Less
Review Section/Research Field	Principal Investigator Pediatrics / Basic Section 52050:Embryonic medicine and pediatrics-related Except Principal Investigator Pediatrics / Neurophysiology and muscle physiology / Biological Sciences
Keywords	Principal Investigator てんかん / 小児神経学 / 難治てんかん / 神経細胞死 / 酸化ストレス / 熱性痙攣 / 炎症 / 熱性けいれん / けいれん重積 / 急性脳症 … More / チャネル異常 / CACNA1A遺伝子 / SCN1A遺伝子 / 神経伝達物質 / チャネル病 / 発達障害 / CACNA1A / SCN1A / パッチクランプ / 難治 / チャネル / ナトリウムチャネル / パッチクランプ法 / 電位依存性ナトリウムチャネル / 神経分子病態学 / 神経疾患の病態と治療 / 精神 … More Except Principal Investigator RGS2 / SMEI / 熱性けいれん / オキシトシン / 脳神経疾患 / 年齢依存性てんかん / 疾患モデル動物 / てんかん / 酸化ストレス / 疾患モデルラット / 発達性およびてんかん性脳症 / anxiety / restrain stress / Oxytocin / PKC / マイクロアレイ / 記憶・学習 / シナプス可塑性 / 不安制御 / 閉所ストレス / Rgs2 / hot water-induced seizure / gene / fever / functional analysis / febrile seizure / SCN1A mutations / severe myoclonic epilepsy in infancy / ミオクローヌス / 入浴けいれん / 遺伝子 / 発熱 / 機能解析 / SCN1A遺伝子変異 / 乳児重症ミオクロニーてんかん / 発熱感受性 / 呼吸性アルカローシス / 二酸化炭素吸入療法 / SCN1A遺伝子 / 電位依存性ナトリウムチャネル / DNAアレイ / 記憶 / 情動 / 扁桃腺 / 海馬 / 脳内ホルモン Less

酸化ストレスによる神経細胞死とてんかん発症機序に関する多層オミックス解析Principal Investigator
- Principal Investigator
  
  大守伊織
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Okayama University
Study of the pathogenesis of west syndrome using a new model rat
- Principal Investigator
  
  Ouchida Mamoru
- Project Period (FY)
  2016 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Okayama University
Development of a animal model of acute encephalopathy and an antibody therapyPrincipal Investigator
- Principal Investigator
  
  Ohmori Iori
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Pediatrics
- Research Institution
  Okayama University
  Kyoto University
New approaches of treating developmental disorders in channelopathyPrincipal Investigator
- Principal Investigator
  
  OHMORI Iori
- Project Period (FY)
  2011 – 2012
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Pediatrics
- Research Institution
  Okayama University
Molecular basis of febrile seizure and new treatment
- Principal Investigator
  
  INOUE Takushi
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Okayama University
Genetic modifiers of an intractable epilepsy with channel gene mutationsPrincipal Investigator
- Principal Investigator
  
  OMORI Iori
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Okayama University
脳内ホルモンによる情動行動の調節とその分子機構
- Principal Investigator
  
  MATSUI Hideki
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Okayama University
Molecular mechanism of loss-of-function SCN1A mutations associated with epilepsyPrincipal Investigator
- Principal Investigator
  
  OOMORI Iori
- Project Period (FY)
  2006 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Okayama University
Oxytocin regulates stress response and anxiety through functional modulation of amygdala
- Principal Investigator
  
  MATSUI Hideki
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Neurophysiology and muscle physiology
- Research Institution
  OKAYAMA UNIVERSITY
Early diagnosis and genetic analysis of severe myoclonic epilepsy in infancy
- Principal Investigator
  
  OHTSUKA Yoko
- Project Period (FY)
  2004 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Okayama University

[Journal Article] Thioredoxin deficiency increases oxidative stress and causes bilateral symmetrical degeneration in rat midbrain.2022
- Author(s)
  Ohmori I, Ouchida M, Imai H, Ishida S, Toyokuni S, Mashimo T.
- Journal Title
  
  Neurobiology of disease
  
  Volume: 175 Pages: 105921-105921
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K07914
[Journal Article] Novel animal model of combined generalized and focal epilepsy.2022
- Author(s)
  Ohmori I, Ouchida M, Shinohara M, Kobayashi K, Ishida S, Mashimo T.
- Journal Title
  
  Epilepsia
  
  Volume: 63 Issue: 7
- DOI
  10.1111/epi.17295
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K07914, KAKENHI-PROJECT-22H04922, KAKENHI-PROJECT-18KK0307
[Journal Article] Cytokine-related and sodium channel polymorphism as candidate predisposing factors for childhood encephalopathy FIRES/AERRPS2016
- Author(s)
  Saitoh, M., Kobayashi, K., Ohmori, I., Tanaka, Y., Tanaka, K., Inoue, T., Horino, A., Ohmura, K., Kumakura, A., Takei, Y., Hirabayashi, S., Kajimoto, M., Uchida, T., Yamazaki, S., Shiihara, T., Kumagai, T., Kasai, M., Terashima, H., Kubota, M., Mizuguchi, M.
- Journal Title
  
  Journal of the Neurological Sciences
  
  Volume: 368 Pages: 272-276
- DOI
  10.1016/j.jns.2016.07.040
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-15H05874, KAKENHI-PROJECT-15H04872, KAKENHI-PROJECT-16K09984, KAKENHI-INTERNATIONAL-15K21731, KAKENHI-PROJECT-26670500
[Journal Article] Action potentials contribute to epileptic high-frequency oscillations recorded with electrodes remote from neurons.2015
- Author(s)
  Kobayashi K, Akiyama T, Ohmori I, Yoshinaga H, Gotman J.
- Journal Title
  
  Clin Neurophysiol.
  
  Volume: 126 Issue: 5 Pages: 873-881
- DOI
  10.1016/j.clinph.2014.08.010
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26670500
[Journal Article] Methylphenidate improves learning impairments and hyperthermia-induced seizures caused by an Scn1a mutation.2014
- Author(s)
  Ohmori, I., Kawakami, N., Liu, S., Wang, H., Miyazaki, I., Asanuma, M., Michiue, H., Matsui, H., Mashimo, T. and Ouchida, M.
- Journal Title
  
  Epilepsia
  
  Volume: 55 Issue: 10 Pages: 1558-1567
- DOI
  10.1111/epi.12750
- NAID
  120005522498
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24659431, KAKENHI-PROJECT-25461279, KAKENHI-PROJECT-26670500
[Journal Article] CACNA1A variants may modify the epileptic phenotype of Dravet syndrome.2013
- Author(s)
  Ohmori I, Ouchida M, Kobayashi K, Jitsumori Y, Mori A, Michiue H, Nishiki T, Ohtsuka Y, Matsui H.
- Journal Title
  
  Neurobiol Dis
  
  Volume: 50 Pages: 209-17
- NAID
  120006765089
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659522
[Journal Article] Inhalation of 10% carbon dioxide rapidly terminates Scn1a mutation-related hyperthermia-induced seizures2013
- Author(s)
  Ohmori I, Hayashi K, Wang H, Ouchida M, Fujita N, Inoue T, Michiue H, Nishiki T, Matsui H
- Journal Title
  
  Epilepsy Res
  
  Volume: in press Issue: 1-2 Pages: 999-999
- DOI
  10.1016/j.eplepsyres.2013.01.003
- NAID
  120006765093
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591130, KAKENHI-PROJECT-23659522
[Journal Article] CACNA1A variants may modify the epileptic phenotype of Dravet syndrome.2013
- Author(s)
  Ohmori I
- Journal Title
  
  Neurobiol Dis.
  
  Volume: 50 Pages: 209-217
- DOI
  10.1016/j.nbd.2012.10.016
- NAID
  120006765089
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659522
[Journal Article] Ca(2+)-independent syntaxin binding to the C(2)B effector region of synaptotagmin.2012
- Author(s)
  4)Masumoto T, Suzuki K, Ohmori I, Michiue H, Tomizawa K, Fujimura A, Nishiki TI, Matsui H.
- Journal Title
  
  Mol Cell Neurosci
  
  Volume: 49 Pages: 1-8
- NAID
  120005425639
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659522
[Journal Article] Additional information regarding "Dravet syndrome: Inroads into understanding epileptic encephalopathies"2012
- Author(s)
  Kobayashi K, Ohtsuka Y, Ohmori I.
- Journal Title
  
  J Pediatr
  
  Volume: 160(3) Issue: 3 Pages: 532-3
- DOI
  10.1016/j.jpeds.2011.11.058
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659522
[Journal Article] Acute encephalopathy in children with Dravet syndrome.2012
- Author(s)
  Okumura A, Uematsu M, Imataka G, Tanaka M, Okanishi T, Kubota T, Sudo A, Tohyama J, Tsuji M, Ohmori I, Naiki M, Hiraiwa-Sofue A, Sato H, Saitoh S, Shimizu T.
- Journal Title
  
  Epilepsia
  
  Volume: 53 Issue: 1 Pages: 79-86
- DOI
  10.1111/j.1528-1167.2011.03311.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591518, KAKENHI-PROJECT-23659522
[Journal Article] Antidepressant-like effect of sildenafil through oxytocin-dependent cyclic AMP response element-binding protein phosphorylation.2012
- Author(s)
  Matsushita H, Matsuzaki M, Han XJ, Nishiki TI, Ohmori I, Michiue H, Matsui H, Tomizawa K.
- Journal Title
  
  Neuroscience
  
  Volume: 200 Pages: 13-18
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659522
[Journal Article] Additional information regarding "Dravet syndrome : Inroads into understanding epileptic encephalopathies"2012
- Author(s)
  Kobayashi K, Ohtsuka Y, Ohmori I
- Journal Title
  
  J Pediatr.
  
  Volume: 160(3) Pages: 532-533
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390312
[Journal Article] High-frequency EEG oscillations in hyperthermia-induced seizures of Scn1a mutant rats.2012
- Author(s)
  Kobayashi K
- Journal Title
  
  Epilepsy Research
  
  Volume: 103 Issue: 2-3 Pages: 161-166
- DOI
  10.1016/j.eplepsyres.2012.07.020
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591130, KAKENHI-PROJECT-23659522
[Journal Article] Additional information regarding "Dravet syndrome: Inroads into understanding epileptic encephalopathies"2012
- Author(s)
  Kobayashi K, Ohtsuka Y, Ohmori I
- Journal Title
  
  J Pediatr
  
  Volume: 160 Pages: 532-533
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659522
[Journal Article] Acute encephalopathy with a novel point mutation in the SCN2A gene2012
- Author(s)
  Kobayashi K, Ohzono H, Shinohara M, Saitoh M, Ohmori I, Ohtsuka Y, Mizuguchi M.
- Journal Title
  
  Epilepsy Res
  
  Volume: 102(1-2) Issue: 1-2 Pages: 109-12
- DOI
  10.1016/j.eplepsyres.2012.04.016
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659522, KAKENHI-PROJECT-22591176
[Journal Article] High-frequency EEG oscillations in hyperthermia-induced seizures of Scn1a mutant rats2012
- Author(s)
  Kobayashi K, Ohmori I, Hayashi K, Kitagawa Y, Ouchida M, Inoue T, Ohtsuka Y
- Journal Title
  
  Epilepsy Res
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591130
[Journal Article] Dravet syndrome with an exceptionally good seizure outcome in two adolescents2011
- Author(s)
  Kobayashi K, Ohmori I, Ouchida M, Ohtsuka Y
- Journal Title
  
  Epileptic Disord
  
  Volume: 13(3) Pages: 340-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390312
[Journal Article] Therapy for hyperthermia-induced seizures in Scn1a mutant rats.2011
- Author(s)
  Hayashi K, Ueshima S, Ouchida M, Mashimo T, Nishiki T, Sendo T, Serikawa T, Matsui H, Ohmori I
- Journal Title
  
  Epilepsia.
  
  Volume: 52 Pages: 1010-1017
- NAID
  130004505757
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659522
[Journal Article] The rapy for hyper ther mia-induced seizures in Scn1a mutant rats2011
- Author(s)
  Hayashi K, Ueshima S, Ouchida M, Mashimo T, Nishiki T, Sendo T, Serikawa T, Matsui H, Ohmori I
- Journal Title
  
  Epilepsia
  
  Volume: 52(5) Issue: 5 Pages: 1010-1017
- DOI
  10.1111/j.1528-1167.2011.03046.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20240042, KAKENHI-PROJECT-21680037, KAKENHI-PROJECT-23659522
[Journal Article] Dravet syndrome with an exceptionally good seizure outcome in two adolescents.2011
- Author(s)
  Kobayashi K, Ohmori I,Ouchida M, Ohtsuka Y.
- Journal Title
  
  Epileptic Disord
  
  Volume: 13(3) Issue: 3 Pages: 340-4
- DOI
  10.1684/epd.2011.0453
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659522
[Journal Article] Acute Encephalopathy in Children with Dravet Syndrome2011
- Author(s)
  Okumura A, Uematsu M, Imataka G, Tanaka M, OkanishiT, KubotaT, SudoA, Tohyama J, Tsuji M, Ohmori I, Naiki M, Hiraiwa-Sofue A, Sato H, Saitoh S, Shimizu T
- Journal Title
  
  Epilepsia
  
  Volume: 53(1) Pages: 79-86
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390312
[Journal Article] Therapy for hyperthermia-induced seizures in Scn1a mutant rats2011
- Author(s)
  Hayashi K, Ueshima S, Ouchida M, Mashimo T, Nishiki T, Sendo T, Serikawa T, Matsui H, Ohmori I
- Journal Title
  
  Epilepsia
  
  Volume: 52(5) Pages: 1010-7
- NAID
  120005468280
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390312
[Journal Article] Dravet syndrome with an exceptionally good seizure outcome in two adolescents.2011
- Author(s)
  Kobayashi K, Ohmori I, Ouchida M, Ohtsuka Y.
- Journal Title
  
  Epileptic Disord.
  
  Volume: 13 Pages: 340-344
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659522
[Journal Article] Acute Encephalopathy in Children with Dravet Syndrome2011
- Author(s)
  Okumura A, Uematsu M, Imataka G, Tanaka M, Okanishi T, Kubota T, Sudo A, Tohyama J, Tsuji M, Ohmori I, Naiki M, Hiraiwa-Sofue A, Sato H, Saitoh S, Shimizu T.
- Journal Title
  
  Epilepsia
  
  Volume: 53 Pages: 79-86
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659522
[Journal Article] ナトリウムチャネル遺伝子Scn1a変異ラットの開発解析研究2010
- Author(s)
  芹川忠夫, 大守伊織, 大内田守, 大野行弘, 鶴見東志子, 三木崇史, 若森実, 石原靜, 吉田卓史, 滝沢明子, 加藤めぐみ, 平林真澄, 笹征史, 森泰生, 真下知士
- Journal Title
  
  てんかん治療研究振興財団研究年報
  
  Volume: 第21集 Pages: 29-36
- Data Source
  KAKENHI-PROJECT-21390312
[Journal Article] Genetic seizure susceptibility underlying acute encephalopathies in childhood2010
- Author(s)
  Kobayashi K, Ouchida M, Okumura A, Maegaki Y, Nishiyama I, Matsui H, Ohtsuka Y, Ohmori I
- Journal Title
  
  Epilepsy Res
  
  Volume: 91 Pages: 143-152
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390312
[Journal Article] A missense mutation of the gene encoding voltage-dependent sodium channel(Na_v1. 1) confers susceptibility to febrile seizures in rats2010
- Author(s)
  Mashimo T, Ohmori I, Ouchida M, Ohno Y, Tsurumi T, Miki T, Wakamori M, Takizawa A, Kato M, Hirabayashi M, Sasa M, Mori Y, Serikawa T
- Journal Title
  
  J Neurosci
  
  Volume: 30 Pages: 5744-5753
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390312
[Journal Article] てんかん関連変異型ナトリウムチャネルNa v1. 1に対する抗てんかん薬の薬理効果2010
- Author(s)
  大守伊織、林桂一郎
- Journal Title
  
  てんかん治療研究振興財団研究年報
  
  Volume: 第21集 Pages: 43-48
- Data Source
  KAKENHI-PROJECT-21390312
[Journal Article] Dravet症候群患者に認められたカルシウムチャネル機能異常を引き起こす2009
- Author(s)
  大守伊織, 大内田守, 以下4人略
- Journal Title
  
  CACNB4遺伝子変異岡山医学会雑誌
  
  Volume: 1213 Pages: 149-156
- Data Source
  KAKENHI-PROJECT-21390312
[Journal Article] (Corresponding author). A Screening test for the prediction of Dravet syndrome before one year of age2008
- Author(s)
  Hattori J, Ouchida M, Ono J, Miyake S, Maniwa S, Mimaki N, Ohtsuka Y, Ohmori I
- Journal Title
  
  Epilepsia 49
  
  Pages: 626-633
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591154
[Journal Article] A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy2008
- Author(s)
  Ohmori I, Ouchida M, Miki T, Mimaki N, Kiyonaka S, Nishiki T, Tomizawa K, Mori Y, Matsui H
- Journal Title
  
  Neurobiol Dis 32
  
  Pages: 349-354
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591154
[Journal Article] Rasmussen encephalitis associated with SCN1A mutation.2008
- Author(s)
  Ohmori I, Ouchida M, Kobayashi K, Jitsumori Y, Inoue T, Shimizu K, Matsui H, Ohtsuka Y, Maegaki Y.
- Journal Title
  
  Epilepsia 49
  
  Pages: 521-526
- NAID
  120006765094
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591154
[Journal Article] A Screening test for the prediction of Dravet syndrome before one year of age.2008
- Author(s)
  Hattori J, Ouchida M, Ono I, Miyake S, Maniwa s, Minaki N, Ohlsuka Y, Ohmori I.
- Journal Title
  
  Epilepsia 49
  
  Pages: 626-633
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591154
[Journal Article] A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy.2008
- Author(s)
  Ohmori I, Ouchida M, Miki T, Mimaki N, Kiyonaka s, Nishiki T, Tomizawa K, Mori Y, Matsui H.
- Journal Title
  
  Neurobiol Dis 32
  
  Pages: 349-354
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591154
[Journal Article] Rasmussen encephalitis associated with SCN1A mutation2008
- Author(s)
  Ohmori I, Ouchida M, Kobayashi K, Jitsumori Y, Inoue T, Shimizu K, Matsui H, Ohtsuka Y, Maegaki Y
- Journal Title
  
  Epilepsia 49
  
  Pages: 521-526
- NAID
  120006765094
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591154
[Journal Article] Rasmussen encephalitis associated with SCNIA mutation.2008
- Author(s)
  Ohmori I, Ouchida M, Kobayashi K, Jitsumori Y, Inoue T, Shimizu K, Matsui H, Ohtsuka Y, Maegaki Y.
- Journal Title
  
  Epilepsia 49
  
  Pages: 521-526
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591154
[Journal Article] A Screening test for the prediction of Dravet syndrome before one year of age.2008
- Author(s)
  Hattori J, Ouchida M, Ono J, Miyake S, Maniwa S, Mimaki N, Ohtsuka Y, Ohmori I.
- Journal Title
  
  Epilepsia (印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591154
[Journal Article] 乳児重症ミオクロニーてんかんとその辺縁てんかん症候群におけるSCN1A遺伝子異常2007
- Author(s)
  大内田守、大守伊織
- Journal Title
  
  てんかん治療研究振興財団研究年報第18集
  
  Pages: 13-19
- Data Source
  KAKENHI-PROJECT-18591154
[Journal Article] Truncations of amphiphysin I by calpain inhibit vesicle endocytosis during neural hyperexcitation2007
- Author(s)
  Wu Y, Liang S, Oda Y, Ohmori I, Nishiki T, Takei K, Matsui H, Tomizawa K
- Journal Title
  
  EMBO J 26
  
  Pages: 2981-90
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591154
[Journal Article] 乳児重症ミオクロニーてんかんとその辺縁てんかん症候群におけるSCN1A遺伝子異常.2007
- Author(s)
  大内田守、大守伊織.
- Journal Title
  
  てんかん治療研究振興財団研究年報 18
  
  Pages: 13-19
- Data Source
  KAKENHI-PROJECT-18591154
[Journal Article] Truncations of amphiphysin I by calpain inhibit vesicle endocytosis during neural hyperexcitation.2007
- Author(s)
  Wu Y-M, Liang S, Oda Y, Ohmori I, Nishiki T, Takei K, Matsui H, Tomizawa K.
- Journal Title
  
  EMBO J. (in press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17300127
[Journal Article] 乳児重症ミオクロニーてんかんにおける変異遺伝子の検索とイオンチャネルの機能解析2006
- Author(s)
  大内田守, 大守伊織, 大塚頌子
- Journal Title
  
  (財)てんかん治療研究振興財団研究年報第17集 2005 17(印刷中)
- Data Source
  KAKENHI-PROJECT-16591030
[Journal Article] Nonfunctional SCN1A is common in severe myoclonic epilepsy of infancy.2006
- Author(s)
  Ohmori I, Kahlig KM, Rhodes TH et al.
- Journal Title
  
  Epilepsia 47
  
  Pages: 1636-1542
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16591030
[Journal Article] Nonfunctional SCN1A is common in severe myoclonic epilepsy of infancy2006
- Author(s)
  Ohmori I, Kahlig KM, Rhodes TH, Wang DW, George AL Jr
- Journal Title
  
  Epilepsia 47
  
  Pages: 1636-42
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591154
[Journal Article] Nonfunctional SCN1A is common in severe myoclonic epilepsy of infancy2006
- Author(s)
  Iori Ohmori
- Journal Title
  
  Epilepsia 47(10)
  
  Pages: 1636-1642
- Data Source
  KAKENHI-PROJECT-18591154
[Journal Article] 乳児重症ミオクロニーてんかんにおける変異遺伝子の検索と変異型イオンチャネルの機能解析2006
- Author(s)
  大内田守, 大守伊織, 大塚頌子
- Journal Title
  
  てんかん治療研究振興財団研究年報 17
  
  Pages: 55-61
- Data Source
  KAKENHI-PROJECT-16591030
[Journal Article] 乳児重症ミオクロニーてんかんにおける変異遺伝子の検索と変異型イオンチャネルの機能解析2006
- Author(s)
  大内田守、大守伊織、大塚頌子
- Journal Title
  
  てんかん治療研究振興財団研究年報第17集
  
  Pages: 55-62
- Data Source
  KAKENHI-PROJECT-18591154
[Journal Article] Nonfunctional SCN1A is common in severe myoclonic epilepsy of infancy2006
- Author(s)
  Ohmori I, Kahlig KM, Rhodes TH et al.
- Journal Title
  
  Epilepsia 47
  
  Pages: 1636-1642
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16591030
[Journal Article] 乳児重症ミオクロニーてんかんにおける変異遺伝子の検索と変異型イオンチャネルの機能解析2006
- Author(s)
  大内田守, 大守伊織, 大塚頌子
- Journal Title
  
  てんかん治療研究財団研究年報 17
  
  Pages: 55-61
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16591030
[Journal Article] Mutation screening and functional analysis for sodium channel alpha 1 subunit in severe myoclonic epilepsy in infancy2006
- Author(s)
  Ouchida M, Ohmori I, Ohtsuka Y
- Journal Title
  
  Ann Rep Jpn Epi Res Found 17
  
  Pages: 55-62
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16591030
[Journal Article] Nonfunctional SCN1A is common in severe myoclonic epilepsy of infancy2006
- Author(s)
  Ohmori I, Kahlig KM, Rhodes TH, Wang DW, George Jr. AL
- Journal Title
  
  Epilepsia 47
  
  Pages: 1636-1642
- Data Source
  KAKENHI-PROJECT-16591030
[Journal Article] Sodium channel dysfunction in intractable childhood epilepsy with generalized tonic-clonic seizures2005
- Author(s)
  Rhodes TH, Vanoye CG, Ohmori I et al.
- Journal Title
  
  J Physiol 569
  
  Pages: 433-445
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16591030
[Journal Article] Sodium channel dysfunction in intractable childhood epilepsy with generalized tonic-clonic seizures.2005
- Author(s)
  Rhodes TH, Vanoye CG, Ohmori I et al.
- Journal Title
  
  J Physiol 569
  
  Pages: 433-445
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16591030
[Journal Article] Relationship between typical and borderline severe myoclonic epilepsy in infancy2005
- Author(s)
  Ohtsuka Y, Ohmori I, Ogino T, Kobayashi K, Oka E
- Journal Title
  
  Epilepsia (In press)
- Data Source
  KAKENHI-PROJECT-16591030
[Journal Article] Mutation screen of GABRA1, GABRB2 and GABRG2 genes in Japanese patients with absence seizures2005
- Author(s)
  Ito M, Ohmori I, Nakahori T et al.
- Journal Title
  
  Neurosci Lett 383
  
  Pages: 220-224
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16591030
[Journal Article] Mutation screen of GABRA1, GABRB2 and GABRG2 genes in Japanese patients with absence seizures.2005
- Author(s)
  Ito M, Ohmori I, Nakahori T et al.
- Journal Title
  
  Neurosci Lett 383
  
  Pages: 220-224
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16591030
[Journal Article] Relationship between typical and borderline severe myoclonic epilepsy in infancy2005
- Author(s)
  Ohtsuka Y, Ohmori I, Ogino T, Kobayashi K, Oka E
- Journal Title
  
  Epilepsia 46(Suppl.2)
  
  Pages: 11-12
- Data Source
  KAKENHI-PROJECT-16591030
[Patent] 遺伝子改変非ヒトモデル動物2018
- Inventor(s)
  大守伊織、大内田守、真下知二
- Industrial Property Rights Holder
  大守伊織、大内田守、真下知二
- Industrial Property Rights Type
  特許
- Filing Date
  2018
- Overseas
- Data Source
  KAKENHI-PROJECT-16H05354
[Patent] 抗てんかん薬2018
- Inventor(s)
  大内田守、大守伊織
- Industrial Property Rights Holder
  大守伊織
- Industrial Property Rights Type
  特許
- Filing Date
  2018
- Acquisition Date
  2019
- Data Source
  KAKENHI-PROJECT-16H05354
[Patent] 遺伝子改変非ヒトモデル動物2017
- Inventor(s)
  大守伊織、真下知士、大内田守
- Industrial Property Rights Holder
  大守伊織、真下知士、大内田守
- Industrial Property Rights Type
  特許
- Industrial Property Number
  2017-238612
- Filing Date
  2017
- Data Source
  KAKENHI-PROJECT-16H05354
[Patent] てんかん波を伴う疾患治療剤2015
- Inventor(s)
  大守伊織，大内田守，改田祐子
- Industrial Property Rights Holder
  大守伊織，大内田守，改田祐子
- Industrial Property Rights Type
  特許
- Filing Date
  2015-08-04
- Data Source
  KAKENHI-PROJECT-26670500
[Patent] てんかん波を伴う疾患治療剤2015
- Inventor(s)
  大守伊織，大内田守，改田祐子
- Industrial Property Rights Holder
  大守伊織，大内田守，改田祐子
- Industrial Property Rights Type
  特許
- Filing Date
  2015-09-03
- Overseas
- Data Source
  KAKENHI-PROJECT-26670500
[Patent] てんかん波を伴う疾患治療剤2011
- Inventor(s)
  大内田守, 大守伊織, 改田祐子
- Industrial Property Rights Holder
  岡山大学
- Filing Date
  2011-07-12
- Overseas
- Data Source
  KAKENHI-PROJECT-21390312
[Patent] てんかん波を伴う疾患治療剤2011
- Inventor(s)
  大内田守、大守伊織、改田祐子
- Industrial Property Rights Holder
  岡山大学
- Filing Date
  2011
- Overseas
- Data Source
  KAKENHI-PROJECT-23659522
[Patent] Dravet 症候群の発症可能性の判定方法およびその利用2011
- Inventor(s)
  大守伊織, 大内田守
- Industrial Property Rights Holder
  岡山大学
- Filing Date
  2011-01-27
- Overseas
- Data Source
  KAKENHI-PROJECT-23659522
[Patent] てんかん波を伴う疾患治療剤2011
- Inventor(s)
  大内田守, 大守伊織, 改田祐子
- Industrial Property Rights Holder
  岡山大学
- Filing Date
  2011-07-12
- Overseas
- Data Source
  KAKENHI-PROJECT-23659522
[Patent] てんかん波を伴う疾患治療剤2011
- Inventor(s)
  大内田守,大守伊織,改田祐子
- Industrial Property Rights Holder
  岡山大学
- Filing Date
  2011-07-12
- Overseas
- Data Source
  KAKENHI-PROJECT-21390312
[Patent] ドラベ症候群の発症可能性の判定方法およびその利用2011
- Inventor(s)
  大守伊織,大内田守
- Industrial Property Rights Holder
  岡山大学
- Filing Date
  2011-01-27
- Overseas
- Data Source
  KAKENHI-PROJECT-21390312
[Patent] ドラベ症候群の発症可能性の判定方法およびその利用2010
- Inventor(s)
  大守伊織,大内田守
- Industrial Property Rights Holder
  岡山大学
- Industrial Property Number
  2010-018705
- Filing Date
  2010-01-29
- Data Source
  KAKENHI-PROJECT-21390312
[Patent] ドラベ症候群の早期診断を可能にするためのデータを取得する方法及びその利用2010
- Inventor(s)
  大守伊織,大内田守,大塚頌子
- Industrial Property Rights Holder
  岡山大学
- Acquisition Date
  2010-02-26
- Data Source
  KAKENHI-PROJECT-21390312
[Patent] てんかん波を伴う疾患治療剤2010
- Inventor(s)
  大内田守,大守伊織,改田祐子
- Industrial Property Rights Holder
  岡山大学
- Industrial Property Number
  2010-164770
- Filing Date
  2010-07-22
- Data Source
  KAKENHI-PROJECT-21390312
[Patent] 脳炎または脳症の罹患リスク判定データの取得方法およびその利用、並びに熱性けいれんのてんかんへの移行リスク判定データの取得方法およびその利用2008
- Inventor(s)
  大守伊織、大内田守
- Industrial Property Rights Holder
  岡山大学
- Industrial Property Number
  2008-274887
- Filing Date
  2008-10-24
- Data Source
  KAKENHI-PROJECT-18591154
[Patent] 急性脳炎または急性脳症の罹患リスク判定データの取得方法およびその利用2007
- Inventor(s)
  大守伊織、大内田守、森泰生、清中茂樹、三木崇史
- Industrial Property Rights Holder
  岡山大学
- Industrial Property Number
  2007-288978
- Filing Date
  2007-11-06
- Data Source
  KAKENHI-PROJECT-18591154
[Patent] 脳炎または脳症の罹患リスク判定データの取得方法およびその利用2007
- Inventor(s)
  大守伊織, 大内田守
- Industrial Property Rights Holder
  岡山大学
- Industrial Property Number
  2007-288985
- Filing Date
  2007-11-06
- Data Source
  KAKENHI-PROJECT-18591154
[Patent] 脳炎または脳症の罹患リスク判定データの取得方法およびその利用2007
- Inventor(s)
  大守伊織、大内田守
- Industrial Property Rights Holder
  岡山大学
- Industrial Property Number
  2007-288978
- Filing Date
  2007-11-06
- Data Source
  KAKENHI-PROJECT-18591154
[Patent] Dravet症候群の早期診断を可能にするためのデータを取得する方法及びその利用2007
- Inventor(s)
  大守伊織, 大内田守, 大塚頌子
- Industrial Property Rights Holder
  岡山大学
- Industrial Property Number
  2007-007449
- Filing Date
  2007-01-16
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] 抗酸化酵素チオレドキシンの機能低下が引き起こす神経細胞死および腎障害のメカニズム探索2023
- Author(s)
  大守伊織
- Organizer
  文部科学省学術変革領域研究学術研究支援基盤形成生命科学連携推進協議会生命科学４プラットフォーム成果発表会
- Invited
- Data Source
  KAKENHI-PROJECT-22K07914
[Presentation] A Txn1 missense mutation links to epilepsy with vacuolar degeneration2022
- Author(s)
  Ohmori I, Ouchida M, Toyokuni S, Ishida S, Mashimo T.
- Organizer
  39th Congress of the International Union of Physiological Sciences (IUPS)
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K07914
[Presentation] Txn1遺伝子変異ラットのてんかんの表現型2019
- Author(s)
  大守伊織，真下知士，大内田守，内藤有香，今井宏彦，豊國伸哉
- Organizer
  日本てんかん学会
- Data Source
  KAKENHI-PROJECT-16H05354
[Presentation] チオレドキシン機能低下は年齢依存的かつ臓器特異的細胞障害を惹起する2019
- Author(s)
  大守伊織，大内田守，豊國伸哉，真下知士
- Organizer
  2019年度【先端モデル動物支援プラットフォーム】成果発表会
- Data Source
  KAKENHI-PROJECT-16H05354
[Presentation] 年齢依存性てんかん脳症を示すTxn1遺伝子変異ラットの病態解析2019
- Author(s)
  大守伊織,真下知士, 大内田守, 加藤(内藤)有香, 豊國伸哉
- Organizer
  先端モデル動物支援プラットフォーム 2018年度成果発表会
- Data Source
  KAKENHI-PROJECT-16H05354
[Presentation] Txn1における新規ミスセンス変異がひきおこす多臓器障害の解析2018
- Author(s)
  加藤(内藤)有香, 真下知士, 大内田守, 豊國　伸哉,大守伊織
- Organizer
  先端モデル動物プラットフォーム平成30年度若手支援技術講習会
- Data Source
  KAKENHI-PROJECT-16H05354
[Presentation] A Txn1 missense mutation damages multiple organs.2018
- Author(s)
  Iori OHMORI, Tomoji MASHIMO, Mamoru OUCHIDA, Kyoko YAMASHITA, Shinya TOYOKUNI
- Organizer
  第41回日本基礎老化学会大会
- Data Source
  KAKENHI-PROJECT-16H05354
[Presentation] 遺伝子変異ラットの表現型解析2018
- Author(s)
  大守伊織、真下知士、大内田守、山下享子、豊國伸哉
- Organizer
  平成29年度文部科学省新学術領域研究先端モデル動物支援プラットフォーム成果発表会
- Data Source
  KAKENHI-PROJECT-16H05354
[Presentation] 新規Txn1遺伝子ミスセンス変異による多臓器障害2018
- Author(s)
  大守伊織、真下知士、大内田守、山下享子、豊國伸哉
- Organizer
  第71回日本酸化ストレス学会　第18回日本NO学会　合同学術集会
- Data Source
  KAKENHI-PROJECT-16H05354
[Presentation] Electrophysiological study of hyperthermia-induced seizures in Scn1a mutant rats2017
- Author(s)
  大守伊織
- Organizer
  第94回日本生理学会大会
- Place of Presentation
  静岡県浜松市
- Year and Date
  2017-03-28
- Data Source
  KAKENHI-PROJECT-26670500
[Presentation] P/Q型電位依存性カルシウムチャネル変異に伴う発達障害2012
- Author(s)
  大内田守、大守伊織
- Organizer
  第54回日本小児神経学総会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-23659522
[Presentation] SCN9A遺伝子変異/多型がドラベ症候群の臨床型におよぼす影響2012
- Author(s)
  大守伊織,Wang Haijiao,大内田守,小林勝弘,松井秀樹
- Organizer
  第46回日本てんかん学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23659522
[Presentation] 自閉症の病態生理とモデル動物を用いた最新研究2012
- Author(s)
  大守伊織
- Organizer
  旭川荘療育センター児童院医局セミナー
- Place of Presentation
  岡山
- Year and Date
  2012-04-10
- Data Source
  KAKENHI-PROJECT-23659522
[Presentation] 熱性けいれん既往患者におけるSCN9A遺伝子解析2012
- Author(s)
  大守伊織、小林勝弘、大内田守
- Organizer
  第54回日本小児神経学総会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-23659522
[Presentation] Scn1a遺伝子変異ラットにおける発達障害2012
- Author(s)
  大守伊織、大内田守
- Organizer
  第54回日本小児神経学総会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-23659522
[Presentation] Epilepsy-related voltage-gated calcium channel variants Cav2.1 shows a gain-of-function biophysical property.2012
- Author(s)
  Ohmori I, Ouchida M, Kobayashi K, Michiue H, Nishiki T, Matsui H
- Organizer
  第89回日本生理学大会
- Place of Presentation
  松本
- Data Source
  KAKENHI-PROJECT-23659522
[Presentation] てんかん関連電位依存性カルシウムチャネルCav2.1変異は機能獲得特性を示す2012
- Author(s)
  大守伊織
- Organizer
  第89回日本生理学会大会
- Place of Presentation
  松本
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] てんかん関連電位依存性カルシウムチャネルCav2. 1変異は機能獲得特性を示す2012
- Author(s)
  大守伊織, 大内田守, 以下4人略
- Organizer
  第89回日本生理学会大会
- Place of Presentation
  松本
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] Pathophysiology and treatment in a rat model of GEFS+2012
- Author(s)
  Ohmori I
- Organizer
  Epilepsy Forum in Okayama
- Place of Presentation
  岡山
- Year and Date
  2012-02-20
- Data Source
  KAKENHI-PROJECT-23659522
[Presentation] Scn1a遺伝子変異による熱性けいれんの二酸化炭素吸入療法2011
- Author(s)
  大守伊織、大内田守、Wang Haijiao、林桂一郎、松井秀樹
- Organizer
  第45回日本てんかん学会
- Place of Presentation
  新潟
- Data Source
  KAKENHI-PROJECT-23659522
[Presentation] シルデナフィル投与によるオキシトシン分泌を介したオスマウスでの抗うつ作用には海馬におけるMAPキナーゼとCREBのリン酸化経路が関与する2011
- Author(s)
  松崎光博、松下博昭、韓小建、西木禎一、大守伊織、富澤一仁、松井秀樹
- Organizer
  第34回日本神経科学大会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-23659522
[Presentation] てんかん関連変異型電位依存性カルシウムチャネルの電気生理特性2011
- Author(s)
  大守伊織、大内田守、Haijiao Wang、北川雄一郎、道上宏之、松井秀樹
- Organizer
  第34回日本神経科学大会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-23659522
[Presentation] Scn1a遺伝子変異による熱性けいれんの二酸化炭素吸入療法2011
- Author(s)
  大守伊織、大内田守、Wang Haijiao、林桂一郎、松井秀樹
- Organizer
  第45回日本てんかん学会
- Place of Presentation
  新潟
- Data Source
  KAKENHI-PROJECT-22591130
[Presentation] シナプトタグミン 1のSNARE複合体からのCa2+依存性解離2011
- Author(s)
  鈴木孝一朗、増本年男、大守伊織、道上宏之、西木禎一、松井秀樹
- Organizer
  第34回日本神経科学大会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-23659522
[Presentation] 代謝性および呼吸性アシドーシスはCacna1aミスセンス変異ラットの欠神発作を抑制する2011
- Author(s)
  大内田守、改田祐子、大守伊織、上原孝、松井秀樹
- Organizer
  第34回日本神経科学大会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-23659522
[Presentation] 急性脳症における遺伝性けいれん素因とSCN1A遺伝子変異2011
- Author(s)
  大守伊織、小林勝弘、大内田守、奥村彰久、前垣義弘、西山逸子、大塚頌子
- Organizer
  第53回日本小児神経学総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-23659522
[Presentation] 急性脳症における遺伝性けいれん素因とSCN1A遺伝子変異2011
- Author(s)
  大守伊織
- Organizer
  第53回日本小児神経学総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] Scnla遺伝子変異による熱性けいれんの二酸化炭素吸入療法2011
- Author(s)
  大守伊織
- Organizer
  第45回日本てんかん学会
- Place of Presentation
  新潟
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] Scn1a遺伝子変異による熱性けいれんの二酸化炭素吸入療法2011
- Author(s)
  大守伊織, 大内田守, 以下3人略
- Organizer
  第45回日本てんかん学会
- Place of Presentation
  新潟
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] てんかん関連変異型電位依存性カルシウムチャネルの電気生理特性2011
- Author(s)
  大守伊織, 大内田守, 以下5人略
- Organizer
  第34回日本神経科学大会
- Place of Presentation
  横浜
- Year and Date
  2011-09-14
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] 急性脳症における遺伝性けいれん素因とSCN1A遺伝子変異2011
- Author(s)
  大守伊織, 小林勝弘, 大内田守, 以下4名略
- Organizer
  第53回日本小児神経学総会
- Place of Presentation
  新潟
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] Scn1a遺伝子変異ラットを用いた熱性けいれんの個別化治療の開発2010
- Author(s)
  林桂一郎, 大守伊織
- Organizer
  第44回日本てんかん学会
- Place of Presentation
  岡山
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] Scnla Mutant Rats Display Ataxia and Memory Deficit2010
- Author(s)
  劉素梅(代表者大守伊織)
- Organizer
  第87回日本生理学会
- Place of Presentation
  盛岡市
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] ワークショップてんかんモデル動物の研究から臨床応用へ「全般てんかん熱性痙攣プラスモデルラットの開発と臨床研究への応用」2010
- Author(s)
  大守伊織
- Organizer
  第44回日本てんかん学会
- Place of Presentation
  岡山市
- Data Source
  KAKENHI-PROJECT-22591130
[Presentation] Dravet症候群における急性脳症2010
- Author(s)
  奥村彰久, 大守伊織, 以下14人略10番目
- Organizer
  第44回日本てんかん学会
- Place of Presentation
  岡山
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] ワークショップてんかんモデル動物の研究から臨床応用へ「全般てんかん熱性痙攣プラスモデルラットの開発と臨床研究への応用」2010
- Author(s)
  大守伊織
- Organizer
  第44回日本てんかん学会
- Place of Presentation
  岡山市
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] Scnla遺伝子変異ラットを用いた熱性けいれんの個別化治療の開発2010
- Author(s)
  林桂一郎(代表者大守伊織)
- Organizer
  第44回日本てんかん学会
- Place of Presentation
  岡山市
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] Scnla遺伝子変異ラットを用いた抗てんかん薬の熱性けいれん抑制効果2010
- Author(s)
  林桂一郎(代表者大守伊織)
- Organizer
  第87回日本生理学会
- Place of Presentation
  盛岡市
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] 熱性けいれんモデルラットを用いた最適治療薬選択の試み2010
- Author(s)
  林桂一郎, 大守伊織, 西木禎一, 真下知士, 以下2人略
- Organizer
  てんかん学会中国四国地方会
- Place of Presentation
  山口
- Year and Date
  2010-02-13
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] Scn1a遺伝子変異ラットを用いた抗てんかん薬の熱性けいれん抑制効果2010
- Author(s)
  林桂一郎, 大守伊織, 西木禎一, 真下知士, 以下2人略
- Organizer
  第87回日本生理学会
- Place of Presentation
  盛岡
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] 電位依存性ナトリウムチャネルSCN1A遺伝子変異に伴うてんかん2010
- Author(s)
  大守伊織
- Organizer
  第130回日本薬学会
- Place of Presentation
  岡山
- Year and Date
  2010-03-28
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] 電位依存性ナトリウムチャネルSCN1A遺伝子変に伴うてんかん2010
- Author(s)
  大守伊織
- Organizer
  第130回日本薬学会一般シンポジウムてんかん研究の展望～新しい抗てんかん薬の開発に向けて～
- Place of Presentation
  岡山
- Year and Date
  2010-03-28
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] Scn1a変異ラットにおける反復熱性けいれんが脳機能に及ぼす影響2010
- Author(s)
  劉素梅, 大守伊織, 林桂一郎, 真下知士, 以下2人略
- Organizer
  てんかん学会中国四国地方会
- Place of Presentation
  山口
- Year and Date
  2010-02-13
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] Scn1a Mutant Rats Display Ataxia and Memory Deficit2010
- Author(s)
  Liu S, Ohmori I, Hayashi K, Nishiki T, Mashimo T, 以下2人略
- Organizer
  第87回日本生理学会
- Place of Presentation
  盛岡
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] 全般てんかん熱性痙攣プラスモデルラットの開発と臨床研究への応用2010
- Author(s)
  大守伊織
- Organizer
  第44回日本てんかん学会ワークショップてんかんモデル動物の研究から臨床応用へ
- Place of Presentation
  岡山
- Year and Date
  2010-10-15
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] 熱刺激誘発けいれん感受性ラットの開発:新たな熱性けいれんモデルとして2009
- Author(s)
  真下知士, 大守伊織, 大内田守, 以下6人略
- Organizer
  第32回日本神経科学大会
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] Cav2. 1 dysfunction may be a genetic modifier of severe myoclonic epilepsyin infancy2009
- Author(s)
  Ohmori I, Ouchida M, 以下7名略
- Organizer
  36th International Congress of Physiological Sciences
- Place of Presentation
  Kyoto, Japan
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] 2種類のチャネル機能異常をもつ乳児重症ミオクロニーてんかん2009
- Author(s)
  大守伊織, 御牧信義、大内田守
- Organizer
  第51回日本小児神経学会総会
- Place of Presentation
  米子
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] A CACNB4 mutation shows altered Cav2.1 function. may be a genetic modifier of severe myoclonic epilepsy in infancy2009
- Author(s)
  Ohmori Iori
- Organizer
  36th International Congress of Physiological Sciences
- Place of Presentation
  京都
- Year and Date
  2009-08-01
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] 2種類のチャネル機能異をもつ乳児重症ミオクロニーてんかん2009
- Author(s)
  大守伊織
- Organizer
  第51回日本小児神経学会総会
- Place of Presentation
  米子
- Year and Date
  2009-05-29
- Data Source
  KAKENHI-PROJECT-21390312
[Presentation] 乳児重症ミオクロニーてんかんの早期診断スクリーニングテスト2008
- Author(s)
  大守伊織、服部旬里、大内田守、真庭聡、御牧信義、三宅進、大塚頌子
- Organizer
  第50回日本小児神経学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] Pharmacological effects of antiepileptic drugs on mutant Navl. l channels associated with epilepsy.2008
- Author(s)
  Ohmori I, Matsushita H, Nishiki T, Tomizawa K, Matsui H.
- Organizer
  第31回日本神経科学大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] A patient with Rasmussen encephalitis and SCNIA mutation. The 11th Annual M2008
- Author(s)
  Kobayashi K, Ohmori I, Ouchida M, Inoue T, Maegaki Y, Jitsumori Y, Matsui H, Shinizu K, Ohtsuka Y.
- Organizer
  The 11th Annual Meeting of Infantile Seizure Society.
- Place of Presentation
  Otsu
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] Risk factors tor the prediction of Dravet syndrome before one year of age.2008
- Author(s)
  Ohmori I, Hattori J, Ouchida M, Ono J, Miyake s, Mimaki N, Ohtsuka Y.
- Organizer
  The nth Annual Meeting of Infantile Seizure Society.
- Place of Presentation
  Otsu
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] A patient with Rasmussen encephalitis and SCN1A mutation2008
- Author(s)
  Kobayashi K, Ohmori I, Ouchida M, Inoue T, Maegaki Y, Jitsumori Y, Matsui H, Shimizu K, Ohtsuka Y
- Organizer
  The 11th Annual Meeting of Infantile Seizure Society
- Place of Presentation
  Otsu
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] 前垣義弘.SCN1A 変異を認めた Rasmussen 脳炎の1例2008
- Author(s)
  小林勝弘、大守伊織、大内田守、井上拓志、大塚頌子
- Organizer
  第50回日本小児神経学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] SCNIA変異を認めたRasmussen脳炎の1例2008
- Author(s)
  小林勝弘, 大守伊織, 大内田守, 井上拓志, 大塚頌子, 前垣義弘.
- Organizer
  第50回日本小児神経学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] Risk factors for the prediction of Dravet syndrome before one year of age2008
- Author(s)
  Ohmori I, Hattori J, Ouchida M, Ono J, Miyake S, Mimaki N, Ohtsuka Y
- Organizer
  The 11^<th> Annual Meeting of Infantile Seizure Society
- Place of Presentation
  Otsu
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] Pharmacological effects of antiepileptic drugs on mutant Nav1.1 channels associated with epilepsy2008
- Author(s)
  Ohmori I, Matsushita H, Nishiki T, Tomizawa K, Matsui H.
- Organizer
  第31回日本神経科学大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] てんかん関連性ナトリウムチャネル異常の機能喪失機序2007
- Author(s)
  大守伊織、大内田守
- Organizer
  第49回日本小児神経学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] SCN1A missense mutation associated with infantile partial epilepsy.2007
- Author(s)
  Ohmori I, Ouchida M, Kobayashi K, Ohtsuka Y, Shimizu K, Nishiki T, Tomizawa K, Matsui H.
- Organizer
  The 30th Annual Meeting of the Japan Neuroscience Society
- Place of Presentation
  Yokohama
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] SCN1A遺伝子変異I1616Tの臨床型2007
- Author(s)
  服部旬里、御牧信義、大守伊織、大野順子、大内田守、大塚頌子
- Organizer
  第49回日本小児神経学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] 熱性痙攣のSCN1A遺伝子異常2007
- Author(s)
  大内田守、大野順子、大守伊織、服部旬里、三宅進、真庭聡、御牧信義、大塚頌子
- Organizer
  第49回日本小児神経学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] Nonfunctional SCN1A is common in severe myoclonic epilepsy in infancy.2007
- Author(s)
  Ohmori I, Kahlig KM, Rhodes TH, Wang DW, Ouchida M, Matsui H, George AL.
- Organizer
  The 10th Annual Meeting of Infantile Seizure Society
- Place of Presentation
  Tokyo
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] Nonfunctional SCN1A is common in severe myoclonic epilepsy in infancy2007
- Author(s)
  Ohmori I, Kahlig KM, Rhodes TH, Wang DW, Ouchida M, Matsui H, George AL
- Organizer
  The 10^<th> Annual Meeting of Infantile Seizure Society
- Place of Presentation
  Tokyo
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] Trafficking defective SCN1A mutations associated with epilepsy.2007
- Author(s)
  Ohmori I, 0uchida M, Nishiki T, Tomizawa K, Matsui H.
- Organizer
  The 7th International Brain Research Organization.
- Place of Presentation
  Melbourne, Australia.
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] Trafficking defective SCN1A mutations associated with epilepsy2007
- Author(s)
  Ohmori I, Ouchida M, Nishiki T, Tomizawa K, Matsui H
- Organizer
  The 7^<th> International Brain Research Organization
- Place of Presentation
  Melbourne, Australia
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] SCN1A遺伝子変異I1616Tの臨床型2007
- Author(s)
  服部旬里、御牧信義、大守伊織、大野順子、大内田守、大塚頒子.
- Organizer
  第49回日本神経学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] てんかん関連性ナトリウムチャネル異常の機能喪失機序2007
- Author(s)
  大守伊織、大内田守.
- Organizer
  第49回日本神経学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] 熱性痙攣のSCN1A遺伝子異常2007
- Author(s)
  大内田守、大野順子、大守伊織、服部旬里、三宅進、真庭聡、御牧信義、大塚頌子.
- Organizer
  第49回日本神経学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] SCN1A missense mutation associated with infantile partial epilepsy2007
- Author(s)
  OhmoriI, Ouchida M, Kobayashi K, Ohtsuka Y, Shimizu K, Nishiki T, Tomizawa K, Matsui H
- Organizer
  The 30^<th> Annual Meeting of the Japan Neuroscience Society
- Place of Presentation
  Yokohama
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] Sodium channel Nav1.1 dysfunction in childhood neurological disorders2006
- Author(s)
  Ohmori I, Matsui H
- Organizer
  第48回日本小児神経学会総会
- Place of Presentation
  浦安
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] Pharmacological rescue of the trafficking defective Nav1.1 channel2006
- Author(s)
  Ohmori I, Nishiki T, Tomizawa K, Matsui H
- Organizer
  第29回日本神経科学会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] 乳児重症ミオクロニーてんかんとその辺縁てんかん症候群におけるSCN1A遺伝子異常2006
- Author(s)
  大守伊織, 大内田守
- Organizer
  第日29回日本分子生物学会年会
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-18591154
[Presentation] Molecular biology of SCN1A mutation-related epileptic syndromes
- Author(s)
  大守伊織
- Organizer
  第19回韓国てんかんコングレス
- Place of Presentation
  韓国　ソウル
- Year and Date
  2014-06-13 – 2014-06-14
- Invited
- Data Source
  KAKENHI-PROJECT-26670500
[Presentation] A screening test for early diagnosis of Dravet syndrome
- Author(s)
  大守伊織，大内田守
- Organizer
  第48回日本てんかん学会学術集会
- Place of Presentation
  日本，東京
- Year and Date
  2014-10-02 – 2014-10-03
- Invited
- Data Source
  KAKENHI-PROJECT-26670500

1. OUCHIDA Mamoru (80213635)

# of Collaborated Projects: 5 results

# of Collaborated Products: 54 results
2. MATSUI Hideki (30157234)

# of Collaborated Projects: 3 results

# of Collaborated Products: 19 results
3. MASHIMO Tomoji (80397554)

# of Collaborated Projects: 2 results

# of Collaborated Products: 9 results
4. INOUE Takushi (80572990)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
5. OHTSUKA Yoko (10213779)

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results
6. TOMIZAWA Kazuhito (40274287)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
7. NISHIKI Teiichi (70423340)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
8. 荻野竜也 (90335597)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. 松下正之 (30273965)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. 小林勝弘

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
11. 奥村彰久

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
12. 芹川忠夫

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
13. 浅沼幹人

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
14. 宮崎育子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Ohmori Iori 大守 伊織

大守 伊織 オオモリ イオリ

OOMORI Iori 大守 伊織

Research Projects

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Co-Researchers

酸化ストレスによる神経細胞死とてんかん発症機序に関する多層オミックス解析Principal Investigator

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Study of the pathogenesis of west syndrome using a new model rat

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Development of a animal model of acute encephalopathy and an antibody therapyPrincipal Investigator

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New approaches of treating developmental disorders in channelopathyPrincipal Investigator

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Molecular basis of febrile seizure and new treatment

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Genetic modifiers of an intractable epilepsy with channel gene mutationsPrincipal Investigator

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脳内ホルモンによる情動行動の調節とその分子機構

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Molecular mechanism of loss-of-function SCN1A mutations associated with epilepsyPrincipal Investigator

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Oxytocin regulates stress response and anxiety through functional modulation of amygdala

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Early diagnosis and genetic analysis of severe myoclonic epilepsy in infancy

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[Journal Article] Thioredoxin deficiency increases oxidative stress and causes bilateral symmetrical degeneration in rat midbrain.2022

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[Journal Article] Novel animal model of combined generalized and focal epilepsy.2022

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[Journal Article] Cytokine-related and sodium channel polymorphism as candidate predisposing factors for childhood encephalopathy FIRES/AERRPS2016

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Ohmori Iori 大守伊織

大守伊織オオモリイオリ

OOMORI Iori 大守伊織