KONO Satoshi 河野智

Researcher Number	40397386
Other IDs
Affiliation (based on the past Project Information) *help	2014 – 2016: 浜松医科大学, 医学部附属病院, 講師 2012: 浜松医科大学, 医学部附属病院, 講師 2010 – 2011: 浜松医科大学, 医学部附属病院, 助教
Review Section/Research Field	Principal Investigator Neurology Except Principal Investigator Neurology
Keywords	Principal Investigator SLC19A3遺伝子 / ビタミンB1 / チアミントランスポーター / SLC19A3 遺伝子 / ウエルニッケ様脳症 / ビタミン B1 Except Principal Investigator アストロサイト / ヘプシジン / セルロプラスミン / トランスフェリン … More / フェロポルチン / 無セルロプラスミン血症 / 鉄 / ヘファエスチン / 神経変性 / 酸化ストレス / 鉄酸化作用 / マンガン / 亜鉛トランスポーター / 亜鉛 / 封入体 / 肝細胞 / ライソゾーム / セラミド / 脳内鉄蓄積症 / 脂質代謝 / ミトコンドリア / βアミロイド前駆体蛋白質 / アルツハイマー病 / 神経変性症 / 遺伝子発現 / 鉄代謝 / 神経難病 Less

Zinc effect for iron efflux from the neuronal cells
- Principal Investigator
  
  Miyajima Hiroaki
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Hamamatsu University School of Medicine
Regulations on the brain iron cycle in the neurodegenerativedisorders
- Principal Investigator
  
  MIYAJIMA Hiroaki
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Hamamatsu University School of Medicine
Pathological mechanism in Wernicke's-like encephalopathy using SLC19A3 transgenic mousePrincipal Investigator
- Principal Investigator
  
  KONO Satoshi
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Hamamatsu University School of Medicine

All 2017 2016 2015 2014 2013 2012 2011 2010

All Journal Article Presentation Book

[Book] Annual Review 神経 20172017
- Author(s)
  河野智、宮嶋裕明
- Total Pages
  281
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-26461291
[Book] Rosenberg’s Molecular and Genetic Basis of Neurological and Psychiatric Disease.2015
- Author(s)
  Kono S, Miyajima H
- Publisher
  Elsevier, Academic Press
- Data Source
  KAKENHI-PROJECT-26461291
[Book] 無セルロプラスミン血症の鉄過剰とその特徴.日本鉄バイオサイエンス学会(編)慢性肝炎における鉄毒性と除鉄治療.~C 型慢性肝炎を中心に~2012
- Author(s)
  河野智、宮嶋裕明
- Publisher
  医薬ジャーナル社
- Data Source
  KAKENHI-PROJECT-22590926
[Book] 慢性肝炎における鉄毒性と除鉄治療2012
- Author(s)
  河野智
- Total Pages
  223
- Publisher
  医薬ジャーナル
- Data Source
  KAKENHI-PROJECT-22590926
[Journal Article] Direct comparison of manganese detoxification/efflux proteins and molecular characterization of ZnT10 protein as a manganese transporter.2016
- Author(s)
  Nishito Y, Tsuji N, Fujishiro H, Takeda TA, Yamazaki T, Teranishi F, Okazaki F, Matsunaga A, Tuschl K, Rao R, Kono S, Miyajima H, Narita H, Himeno S, Kambe T.
- Journal Title
  
  J Biol Chem
  
  Volume: 291 Pages: 14773-14787
- NAID
  120006376011
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26461291
[Journal Article] Case of presymptomatic aceruloplasminemia treated with deferasirox2014
- Author(s)
  Tai M, Matsuhashi N, Ichii O, Suzuki T, Ejiri Y, Kono S, Terada T, Miyajima H, Harada M
- Journal Title
  
  Hepatol Res
  
  Volume: 44 Pages: 1253-1258
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26461291
[Journal Article] SPG3A-linked hereditary spastic paraplegia associated with cerebral glucose hypometabolism.2013
- Author(s)
  Terada T, Kono S, Ouchi Y, Yoshida K, Hamaya Y, Kanaoka S, Miyajima H
- Journal Title
  
  Ann Nucl Med
  
  Volume: 27(3) Issue: 3 Pages: 303-8
- DOI
  10.1007/s12149-012-0673-5
- NAID
  10031168098
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590927, KAKENHI-PROJECT-23390287, KAKENHI-PROJECT-23659562
[Journal Article] Benign hereditary chorea: dopaminergic brain imaging in patients with a novel intronic NKX2.1 gene mutation2013
- Author(s)
  Konishi T, Kono S, Fujimoto M, Terada T, Matsushita K, Ouchi Y, Miyajima H
- Journal Title
  
  J Neurol
  
  Volume: 260(1) Issue: 1 Pages: 207-13
- DOI
  10.1007/s00415-012-6618-z
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590927
[Journal Article] Vitamin B1と神経疾患　Wernicke様脳症 (thiamine transporter gene mutation)2012
- Author(s)
  河野智
- Journal Title
  
  神経内科
  
  Volume: 76 Pages: 248-254
- Data Source
  KAKENHI-PROJECT-22590927
[Journal Article] In vivo mesolimbic D2/3 receptor binding predicts posttherapeutic clinical responses in restless legs syndrome: a positron emission tomography study2012
- Author(s)
  Oboshi Y, Ouchi Y, Yagi S, Kono S, Nakai N, Yoshikawa E, Futatsubashi M, Terada T, Kim K, Harada K
- Journal Title
  
  J Cereb Blood Flow Metab
  
  Volume: 32(4) Issue: 4 Pages: 654-62
- DOI
  10.1038/jcbfm.2011.201
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590927, KAKENHI-PROJECT-23390287, KAKENHI-PROJECT-23659562
[Journal Article] Combined FDG and raclopride PET study in a case of ALS with the R521C FUS gene mutation2012
- Author(s)
  Kono S, Ouchi Y, Terada T, Suzuki M, Yagi S, Miyajima H.
- Journal Title
  
  J Neurol
  
  Volume: 259(2) Issue: 2 Pages: 367-9
- DOI
  10.1007/s00415-011-6168-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590927
[Journal Article] Vitamin B1 と神経疾患 Wernicke 様脳症2012
- Author(s)
  河野智,白川健太郎,宮嶋裕明
- Journal Title
  
  (thiamine transporter gene mutation)神経内科
  
  Volume: 76 Pages: 248-254
- URL
  http://www.kahyo.com/item/S201203-763
- Data Source
  KAKENHI-PROJECT-22590927
[Journal Article] Subacute progressive ophthalmoplegia associated with dermatomyositis2012
- Author(s)
  Kono S, Bunai T, Terada T, Shimoyama K, Konishi T, Shirakawa K, MiyajimaH
- Journal Title
  
  J Neurol
  
  Volume: 259 Pages: 1982-1984
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590926
[Journal Article] Aceruloplasminemia2012
- Author(s)
  Kono S
- Journal Title
  
  Curr Drug Target
  
  Volume: 13 Pages: 1190-1199
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590926
[Journal Article] Combined FDG and raclopride PET study in a case of ALS with the R521C FUS gene mutation2012
- Author(s)
  Kono S, Ouchi Y, Terada T, Suzuki M, Yagi S, Miyajima H.
- Journal Title
  
  J Neurol
  
  Volume: 259 Pages: 367-369
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590926
[Journal Article] A case of Epstein-Barr virus associated post-transplant lymphoproliferative disorder with CNS involvement: pathological findings at both biopsy and autopsy.2011
- Author(s)
  Suzuki M, Kosugi I, Terada T, Shirakawa K, Suzuki H, Kono S, Miyajima H
- Journal Title
  
  Neuropathol
  
  Volume: 31 Pages: 440-445
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590926
[Journal Article] Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders2010
- Author(s)
  Kaneko Y, Miyajima H, Piperno A, Tomosugi N, Hayashi H, Morotomi N, Tsuchida KI, Ikeda T, Ishikawa A, Ota Y, Wakusawa S, Yoshioka K, Kono S, Pelucchi S, Hattori A, Tatsumi Y, Okada T, Yamagishi M
- Journal Title
  
  J Gastroenterol
  
  Volume: 45 Pages: 1163-1171
- NAID
  10027699891
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590926
[Journal Article] Biological effects of mutant ceruloplasmin on hepcidin-mediated internalization of ferroportin2010
- Author(s)
  Kono S, Yoshida K, Tomosugi N, Terada T, Hamaya Y, Kanaoka S, Miyajima H
- Journal Title
  
  Biochim Biophys Acta.
  
  Volume: 1802(11) Issue: 11 Pages: 968-75
- DOI
  10.1016/j.bbadis.2010.07.011
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590927
[Journal Article] Functional brain imaging in glucocerebrosidase mutation carriers with and without parkinsonism.2010
- Author(s)
  Kono S, Ouchi Y, Terada T, Ida H, Suzuki M, Miyajima H
- Journal Title
  
  Mov Disord.
  
  Volume: 25(12) Issue: 12 Pages: 1823-9
- DOI
  10.1002/mds.23213
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590927
[Journal Article] 家族性 Wernicke 類似脳症2010
- Author(s)
  宮嶋裕明河野智
- Journal Title
  
  臨床神経
  
  Volume: 50 Pages: 855-857
- URL
  http://www.neurology-jp.org/Journal/public_pdf/050110855.pdf
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590927
[Journal Article] Functional brain imaging in glucocerebrosidase mutation carriers with and without parkinsonism2010
- Author(s)
  Kono S, Ouchi Y, Terada T, Ida H, Suzuki M, Miyajima H
- Journal Title
  
  Mov Disord
  
  Volume: 25 Pages: 1823-1829
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590926
[Journal Article] Functional brain imaging in glucocerebrosidase mutation carriers with and without parkinsonism.2010
- Author(s)
  Kono S, Ouchi Y, Terada T, Ida H, Suzuki M, Miyajima H.
- Journal Title
  
  Movement Disorders
  
  Volume: 49
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590927
[Journal Article] Biological effects of mutant ceruloplasmin on hepcidin-mediated internalization of ferroportin.2010
- Author(s)
  Kono S, Yoshida K, Tomosugi N, Terada T, Hamaya Y, Kanaoka S, Miyajima H
- Journal Title
  
  Biochim Biophys Acta
  
  Volume: 1802 Pages: 968-975
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590926
[Journal Article] Biological effects of mutant ceruloplasmin on hepcidin-mediated internalization of ferroportin.2010
- Author(s)
  Kono S, Yoshida K, Tomosugi N, Terada T, Hamaya Y, Kanaoka S, Miyajima H.
- Journal Title
  
  Biochim Biophys Acta
  
  Volume: 1802 Pages: 968-975
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590927
[Journal Article] Central diabetes insipidus and hypothalamic hypothyroidism associated with aceruloplasminemia2010
- Author(s)
  Watanabe M, Asai C, Ishikawa K, Kiyota A, Terada T, Kono S, Miyajima H, Okumura A.
- Journal Title
  
  Intern Med
  
  Volume: 49 Pages: 1581-1585
- NAID
  130000299583
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590926
[Presentation] Combined FDG and raclopride PET study in a case of ALS with the R521C FUS gene mutation2011
- Author(s)
  河野智
- Organizer
  世界神経学会
- Place of Presentation
  モロッコ・マケラシュ
- Year and Date
  2011-11-17
- Data Source
  KAKENHI-PROJECT-22590927

1. MIYAJIMA Hiroaki (90221613)

# of Collaborated Projects: 3 results

# of Collaborated Products: 21 results
2. SUZUKI Makiko (60549278)

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results

KONO Satoshi 河野 智

Research Projects

Research Products

Co-Researchers

Zinc effect for iron efflux from the neuronal cells

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Regulations on the brain iron cycle in the neurodegenerativedisorders

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Pathological mechanism in Wernicke's-like encephalopathy using SLC19A3 transgenic mousePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Book] Annual Review 神経 20172017

Author(s)

Total Pages

Publisher

Data Source

[Book] Rosenberg’s Molecular and Genetic Basis of Neurological and Psychiatric Disease.2015

Author(s)

Publisher

Data Source

[Book] 無セルロプラスミン血症の鉄過剰とその特徴.日本鉄バイオサイエンス学会(編)慢性肝炎における鉄毒性と除鉄治療.~C 型慢性肝炎を中心に~2012

Author(s)

Publisher

Data Source

[Book] 慢性肝炎における鉄毒性と除鉄治療2012

Author(s)

Total Pages

Publisher

Data Source

[Journal Article] Direct comparison of manganese detoxification/efflux proteins and molecular characterization of ZnT10 protein as a manganese transporter.2016

Author(s)

Journal Title

NAID

Data Source

[Journal Article] Case of presymptomatic aceruloplasminemia treated with deferasirox2014

Author(s)

Journal Title

Data Source

[Journal Article] SPG3A-linked hereditary spastic paraplegia associated with cerebral glucose hypometabolism.2013

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] Benign hereditary chorea: dopaminergic brain imaging in patients with a novel intronic NKX2.1 gene mutation2013

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Vitamin B1と神経疾患 Wernicke様脳症 (thiamine transporter gene mutation)2012

Author(s)

Journal Title

Data Source

[Journal Article] In vivo mesolimbic D2/3 receptor binding predicts posttherapeutic clinical responses in restless legs syndrome: a positron emission tomography study2012

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Combined FDG and raclopride PET study in a case of ALS with the R521C FUS gene mutation2012

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Vitamin B1 と神経疾患 Wernicke 様脳症2012

Author(s)

Journal Title

URL

Data Source

[Journal Article] Subacute progressive ophthalmoplegia associated with dermatomyositis2012

KONO Satoshi 河野智

[Journal Article] Vitamin B1と神経疾患　Wernicke様脳症 (thiamine transporter gene mutation)2012