FURUTA HIROTO 古田浩人

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FURUTA Hiroto 古田浩人

古田浩人フルタヒロト

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Researcher Number	90238684
Affiliation (Current)	2022: 和歌山県立医科大学, 医学部, 准教授
Affiliation (based on the past Project Information) *help	2016 – 2021: 和歌山県立医科大学, 医学部, 准教授 2013: 和歌山県立医科大学, 医学部, 准教授 2011 – 2012: 和歌山県立医科大学, 医学部, 講師 2007 – 2008: Wakayama Medical University, 医学部, 講師 2003 – 2004: 和歌山県立医科大学, 医学部, 講師 2000: 和歌山県立医科大学, 医学部, 助手
Review Section/Research Field	Principal Investigator Metabolomics / Basic Section 54040:Metabolism and endocrinology-related Except Principal Investigator Biological Sciences / General internal medicine (including Psychosomatic medicine) / Applied health science / Metabolomics
Keywords	Principal Investigator 糖尿病 / 遺伝因子 / MODY / インクレチン / TCF7L2 遺伝子 / 遺伝子多型 / TCF7L2 / ＭＯＤＹ / インスリン遺伝子 / ABCC８遺伝子 … More / 高インスリン血症性新生児低血糖症 / ABCC8遺伝子 / HNF1A遺伝子 / PAX4 / 遺伝子 / 小胞体ストレス … More Except Principal Investigator 転写因子 / 肥満 / 摂食調節 / 視床下部 / 糖尿病 / SOD / UCP-2 / GPx-1 / BDNF / インスリン抵抗性 / ミニマルモデル / 遺伝子多型 / ストレス / 絶食 / モデルマウス / 神経性食思不振症 / レプチン / グレリン / ベータセルリン / 遺伝要因 / 食欲調節 / Leptin / Diabetes / Ghrelin / Betacellulin / 非アルコール性脂肪肝 / サイトカイン / 運動 / AFF4 / FGF21 / メタボリック症候群 / 糖・脂質代謝 / エネルギー代謝 Less

若年発症糖尿病濃厚家系の原因遺伝子探索と診療への応用Principal Investigator
- Principal Investigator
  
  古田浩人
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 54040:Metabolism and endocrinology-related
- Research Institution
  Wakayama Medical University
Elucidation of causal genes of monogenic diabetes and it applies to the medical treatmentPrincipal Investigator
- Principal Investigator
  
  Furuta Hiroto
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Metabolomics
- Research Institution
  Wakayama Medical University
Role of exercise-induced oncostatin M in the treatment of NASH
- Principal Investigator
  
  Morikawa Yoshihiro
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Applied health science
- Research Institution
  Wakayama Medical University
Roles of AFF4, a member of the AF4 family of transcription factors, in FGF21 resistance
- Principal Investigator
  
  Komori Tadasuke
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Metabolomics
- Research Institution
  Wakayama Medical University
Search for novel MODY genes with exome sequencingPrincipal Investigator
- Principal Investigator
  
  FURUTA Hiroto
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Metabolomics
- Research Institution
  Wakayama Medical University
Functional roles of AF5q31and its relationship with anorexia nervosa.
- Principal Investigator
  
  MORIKAWA Yoshihiro
- Project Period (FY)
  2011 – 2012
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  General internal medicine (including Psychosomatic medicine)
- Research Institution
  Wakayama Medical University
Mechanism of increased risk of type 2 diabetes by TCF7L2 gene polymorphismsPrincipal Investigator
- Principal Investigator
  
  FURUTA Hiroto
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Metabolomics
- Research Institution
  Wakayama Medical University
The Investigation of Genetic Factors Involved in the Pathogeneses and Pathophysiology of Obese Type 2 Diabetes
- Principal Investigator
  
  NANJO Kishio
- Project Period (FY)
  2001 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  WAKAYAMA MEDICAL UNIVERSITY
2型糖尿病患者におけるインスリン抵抗性に関与する遺伝的要因の解析
- Principal Investigator
  
  NANJO Kishio
- Project Period (FY)
  2000
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas (C)
- Review Section
  
  Biological Sciences
- Research Institution
  Wakayama Medical University

[Book] 「すべてがわかる最新・糖尿病」、編集　門脇孝、2011
- Author(s)
  古田浩人（分担執筆）
- Total Pages
  450
- Publisher
  照林社
- Data Source
  KAKENHI-PROJECT-23591319
[Journal Article] A family in which people with a heterozygous ABCC8 gene mutation (p.Lys1385Gln) have progressed from hyperinsulinemic hypoglycemia to hyperglycemia2020
- Author(s)
  Karatojima, M. Furuta, H. Matsutani, N. Matsuno, S. Tamai, M. Komiya, K. Morita, S. Uraki, S. Doi, A. Furuta, M. Iwakura, H. Ariyasu, H. Nishi, M. Akamizu, T.
- Journal Title
  
  J Diabetes
  
  Volume: 12 Pages: 21-24
- DOI
  10.1111/1753-0407.12990
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K09842
[Journal Article] Identification of a compound heterozygous inactivating ABCC8 gene mutation responsible for young-onset diabetes with exome sequencing2020
- Author(s)
  Matsutani, N. Furuta, H. Matsuno, S. Oku, Y. Morita, S. Uraki, S. Doi, A. Furuta, M. Iwakura, H. Ariyasu, H. Nishi, M. Akamizu, T.
- Journal Title
  
  J Diabetes Investig
  
  Volume: 11 Pages: 333-336
- DOI
  10.1111/jdi.13138
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K09842
[Journal Article] 全容が解き明かされつつある糖尿病遺伝素因ー若年発症糖尿病　MODY1-6以外の病因と病態についてー2020
- Author(s)
  古田浩人
- Journal Title
  
  月刊糖尿病
  
  Volume: 12 Pages: 24-30
- Data Source
  KAKENHI-PROJECT-20K08868
[Journal Article] Neonatal diabetes caused by the heterozygous Pro1198Leu mutation in the ABCC8 gene in a male infant: 6-year clinical course2020
- Author(s)
  Uraki S, Furuta H, Miyawaki M, Matsutani N, Shima Y, Iwamoto M, Matsuno S, Morita S, Furuta M, Doi A, Iwakura H, Ariyasu H, Nishi M, Suzuki H, Akamizu T.
- Journal Title
  
  J Diabetes Investig
  
  Volume: 11(2) Pages: 502-505
- DOI
  10.1111/jdi.13127
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-17K09842
[Journal Article] Identification of a variant-associated with early-onset diabetes in the intron of INS gene with exome sequencing2019
- Author(s)
  Matsuno, S., Furuta, H., Kosaka, K., Doi, A., Yorifuji, T., Fukuda, T., Senmaru, T., Uraki, S., Matsutani, N., Furuta, M., Mishima, H., Iwakura, H., Nishi, M., Yoshiura, K., Fukui, M. and Akamizu, T.
- Journal Title
  
  Journal of Diabetes Investigation
  
  Volume: Epub ahead of print Pages: 947-950
- DOI
  10.1111/jdi.12974
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K09842, KAKENHI-PROJECT-18K07850, KAKENHI-PROJECT-19K22913, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-16KT0112
[Journal Article] 糖尿病の遺伝素因―単一遺伝子異常による糖尿病―、インスリン遺伝子異常と糖尿病2019
- Author(s)
  松野正平、松谷紀彦、古田浩人
- Journal Title
  
  糖尿病
  
  Volume: 62 Pages: 468-470
- Data Source
  KAKENHI-PROJECT-17K09842
[Journal Article] Oncostatin M is a potential agent for the treatment of obesity and related metabolic disorders: a study in mice2015
- Author(s)
  Komori T, Tanaka M, Furuta H, Akamizu T, Miyajima A, Morikawa Y
- Journal Title
  
  Diabetologia
  
  Volume: 58 Pages: 1868-1876
- DOI
  10.1007/s00125-015-3613-9
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-15K15115, KAKENHI-PLANNED-26110007, KAKENHI-PROJECT-26282195, KAKENHI-PROJECT-26253023
[Journal Article] Familial young-onset diabetes, pre-diabetes and cardiovascular disease are associated with genetic variants of DACH1 in Chinese.2014
- Author(s)
  Ma RC, Lee HM, Lam VK, Tam CH, Ho JS, Zhao HL, Guan J, Kong AP, Lau E, Zhang G, Luk A, Wang Y, Tsui SK, Chan TF, Hu C, Jia WP, Park KS, Lee HK, Furuta H, Nanjo K, Tai ES, Ng DP, Tang NL, Woo J, Leung PC, Xue H, Wong J, Leung PS, Lau TC, Tong PC, Xu G, Ng MC, So WY, Chan JC
- Journal Title
  
  PLoS One
  
  Volume: 9
- DOI
  10.1371/journal.pone.0084770
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591319
[Journal Article] Familial young-onset diabetes, pre-diabetes and cardiovascular disease are associated with genetic variants of DACH1 in Chinese2014
- Author(s)
  Ma RC, Lee HM, Lam VK, Tam CH, Ho JS, Zhao HL, Guan J, Kong AP, Lau E, Zhang G, Luk A, Wang Y, Tsui SK, Chan TF, Hu C, Jia WP, Park KS, Lee HK, Furuta H, Nanjo K, Tai ES, Ng DP, Tang NL, Woo J, Leung PC, Xue H, Wong J, Leung PS, Lau TC, Tong PC, Xu G, Ng MC, So WY, Chan JC
- Journal Title
  
  PLoS One
  
  Volume: 9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591319
[Journal Article] Clinical and functional characterization of the Pro1198Leu ABCC8 gene mutation associated with permanent neonatal diabetes mellitus2013
- Author(s)
  Takagi T, Furuta H, Miyawaki M, Nagashima K, Shimada T, Doi A, Matsuno S, Tanaka D, Nishi M, Sasaki H, Inagaki N, Yoshikawa N, Nanjo K, Akamizu T
- Journal Title
  
  J Diabetes Invest
  
  Volume: 4 Pages: 269-273
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591319
[Journal Article] The Kir6.2 E23K polymorphism is related to secondary failure of sulfonylureas in non-obese patients with type 2 diabetes.2013
- Author(s)
  Shimajiri Y, Yamana A, Morita S, Furuta H, Furuta M, Sanke T
- Journal Title
  
  J Diabetes Invest
  
  Volume: 4 Pages: 445-449
- DOI
  10.1111/jdi.12070
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591319
[Journal Article] Clinical and functional characterization of the Pro1198Leu ABCC8 gene mutation associated with permanent neonatal diabetes mellitus.2013
- Author(s)
  Takagi T, Furuta H, Miyawaki M, Nagashima K, Shimada T, Doi A, Matsuno S, Tanaka D, Nishi M, Sasaki H, Inagaki N, Yoshikawa N, Nanjo K, Akamizu T.
- Journal Title
  
  J Diabetes Invest
  
  Volume: 4 Pages: 269-273
- DOI
  10.1111/jdi.12049
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591319
[Journal Article] Genetic associations of type 2 diabetes with islet amyloid polypeptide processing and degrading pathways in asian populations.2013
- Author(s)
  Lam VK, Ma RC, Lee HM, Hu C, Park KS, Furuta H, Wang Y, Tam CH, Sim X, Ng DP, Liu J, Wong TY, Tai ES, Morris AP; DIAGRAM Consortium, Tang NL, Woo J, Leung PC, Kong AP, Ozaki R, Jia WP, Lee HK, Nanjo K, Xu G, Ng MC, So WY, Chan JC
- Journal Title
  
  PLoS One
  
  Volume: 8
- DOI
  10.1371/journal.pone.0062378
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591319
[Journal Article] Genetic associations of type 2 diabetes with islet amyloid polypeptide processing and degrading pathways in asian populations2013
- Author(s)
  Lam VK, Ma RC, Lee HM, Hu C, Park KS, Furuta H, Wang Y, Tam CH, Sim X, Ng DP, Liu J, Wong TY, Tai ES, Morris AP; DIAGRAM Consortium, Tang NL, Woo J, Leung PC, Kong AP, Ozaki R, Jia WP, Lee HK, Nanjo K, Xu G, Ng MC, So WY, Chan JC
- Journal Title
  
  PLoS One
  
  Volume: 8(6)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591319
[Journal Article] The Kir6.2 E23K polymorphism is related to secondary failure of sulfonylureas in non-obese patients with type 2 diabetes2013
- Author(s)
  Shimajiri Y, Yamana A, Morita S, Furuta H, Furuta M, Sanke T
- Journal Title
  
  J Diabetes Invest
  
  Volume: 4(5) Pages: 445-449
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591319
[Journal Article] Komori T, Doi A, Nosaka T, Furuta H, Akamizu T, Kitamura T, Senba E, Morikawa Y: Regulation of AMP-activated protein kinase signaling by AFF4, a member of the AF4 (ALL1-fused gene from chromosome 4) family of transcription factors, in hypothalamic neurons.2012
- Author(s)
  Komori T, Doi A, Nosaka T, Furuta H, Akamizu T, Kitamura T, Senba E, Morikawa Y
- Journal Title
  
  J Biol Chem
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591319
[Journal Article] Defective PAX4 R192H transcriptional repressor activities associated with maturity onset diabetes of the young and early onset-age of type 2 diabete.2012
- Author(s)
  Kooptiwut S, Plengvidhya N, Chukijrungroat T, Sujjitjoon J, Semprasert N, Furuta H, Yenchitsomanus PT
- Journal Title
  
  J Diabetes Complications
  
  Volume: 26 Pages: 343-347
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591319
[Journal Article] Defective PAX4 R192H transcriptional repressor activities associated with maturity onset diabetes of the young and early onset-age of type 2 diabete2012
- Author(s)
  Kooptiwut S, Plengvidhya N, Chukijrungroat T, Sujjitjoon J, Semprasert N, Furuta H, Yenchitsomanus PT
- Journal Title
  
  J Diabetes Complications
  
  Volume: 26 Pages: 343-347
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591319
[Journal Article] Regulation of AMP-activated Protein Kinase Signaling by AFF4, a Member of the AF4 (ALL1-fused Gene from Chromosome 4) Family of Transcription Factors, in Hypothalamic Neurons.2012
- Author(s)
  Komori T, Doi A, Nosaka T, Furuta H, Akamizu T, Kitamura T, Senba E, Morikawa Y.
- Journal Title
  
  J. Biol. Chem.
  
  Volume: 287 Pages: 19985-19996
- DOI
  10.1074/jbc.m112.367854
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22390206, KAKENHI-PROJECT-23659385, KAKENHI-PROJECT-24659494
[Journal Article] Pro 198 Leu missense polymorphism of the glutathione peroxidase 1 gene might be a common genetic predisposition of distal symmetric polyneuropathy and macrovascular disease in Japanese type 2 diabetic patient.2011
- Author(s)
  Matsuno S, Sasaki H, Yamazaki H, Yamaoka H, Ogawa K,,Nakatani M, Hamanishi T, Doi A, Nakano Y, Wakasaki H, Furuta H, Nishi M, Akamizu T, Nanjo K
- Journal Title
  
  J Diabetes Invest
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591319
[Journal Article] Nonsense and missense mutations in the human hepatocyte nuclear factor-1β gene (TCF2) and their relation to type 2 diabetes in Japanese2002
- Author(s)
  Furuta H
- Journal Title
  
  J. Clin. Endocrinol. Metab. 87
  
  Pages: 3859-3863
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-13204074
[Journal Article] Nonsense and missense mutations in the human hepatocyte nuclear factor-1 β gene (TCF2) and their relation to type 2 diabetes in Japanese2002
- Author(s)
  Furuta H
- Journal Title
  
  J Clin Endocrinol Metab 87
  
  Pages: 3859-3863
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-13204074
[Presentation] 「臨床医が知っておくべき糖尿病の基礎」遺伝子異常による糖尿病2022
- Author(s)
  古田浩人
- Organizer
  第56回糖尿病学の進歩
- Invited
- Data Source
  KAKENHI-PROJECT-20K08868
[Presentation] 全エクソームシークエンス法を用いて新たに同定したMODYの２家系2021
- Author(s)
  岩橋真子、古田浩人、松野正平、大槻朋子、土井麻子、森田修平、石橋達也、古川安志、岩倉　浩、西　理宏、松岡孝昭
- Organizer
  第58回日本糖尿病学会近畿地方会
- Data Source
  KAKENHI-PROJECT-20K08868
[Presentation] 全エクソームシークエンス法を用いた若年発症糖尿病の遺伝因子探索2021
- Author(s)
  古田浩人、松谷紀彦、松野正平、浦木進丞、土井麻子、森田修平、石橋達也、古川安志、岩倉浩、西理宏、松岡孝昭
- Organizer
  第64回日本糖尿病学会年次学術集会
- Data Source
  KAKENHI-PROJECT-20K08868
[Presentation] 糖尿病の遺伝因子2020
- Author(s)
  古田浩人
- Organizer
  第57回日本糖尿病学会年近畿地方会
- Invited
- Data Source
  KAKENHI-PROJECT-20K08868
[Presentation] HNF-1A遺伝子変異による糖尿病（MODY3）の臨床像の検討2020
- Author(s)
  古田浩人、松谷紀彦、宮脇正和、古田眞智、松野正平、浦木進丞、土井麻子、太田敬之、森田修平、岩倉　浩、西　理宏、鈴木啓之
- Organizer
  第70回日本体質医学会総会
- Data Source
  KAKENHI-PROJECT-20K08868
[Presentation] ABCC8遺伝子変異による新生児糖尿病症例の7年間の臨床経過2020
- Author(s)
  浦木進丞、古田浩人、宮脇正和、岩本美紀、松谷紀彦、松野正平、土井麻子、森田修平、有安宏之、西　理宏、鈴木啓之、赤水尚史
- Organizer
  第63回日本糖尿病学会年次学術集会
- Data Source
  KAKENHI-PROJECT-20K08868
[Presentation] 単一遺伝子異常による糖尿病―その特徴と診療のポイントー2020
- Author(s)
  古田浩人
- Organizer
  第63回日本糖尿病学会年次学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-20K08868
[Presentation] ABCC8遺伝子変異(p.P1198L)による新生児糖尿病症例の6年間の臨床2019
- Author(s)
  浦木進丞、古田浩人、宮脇正和、松野正平、松谷紀彦、土井麻子、有安宏之、西　理宏、鈴木啓之、赤水尚史
- Organizer
  第69回日本体質医学会総会
- Data Source
  KAKENHI-PROJECT-17K09842
[Presentation] HNF1A 遺伝子 p.Arg200Trp ミスセンス変異による MODY3 の１家系2019
- Author(s)
  小瀨川真美、古田浩人、松野正平、浦木進丞、松谷紀彦、土井麻子、森田修平、有安宏之、岩倉　浩、西　理宏、赤水尚史
- Organizer
  第56回日本糖尿病学会近畿地方会
- Data Source
  KAKENHI-PROJECT-17K09842
[Presentation] オクトレオチド持続皮下注射にてコントロール良好な先天性高インスリン血症の１例2019
- Author(s)
  岩本美紀、宮脇正和、向山弘展、比嘉明日美、津野嘉伸、熊谷　健、奥谷貴弘、樋口隆造、古田浩人、赤水尚史、鈴木啓之
- Organizer
  第56回日本糖尿病学会近畿地方会
- Data Source
  KAKENHI-PROJECT-17K09842
[Presentation] Mutations in the sulfonylurea receptor 1 gene and diabetes.2019
- Author(s)
  Furuta H, Matsutani N, Matsuno S, Oku Y, Doi A, Uraki S, Morita S, Furuta M, Nishi M, Akamizu T
- Organizer
  The 11th Scientific Meeting of the Asian Association for the Stuy of Diabetes
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K09842
[Presentation] 個々の病態に応じた糖尿病診療「単一遺伝子異常による糖尿病とその診療」2019
- Author(s)
  古田浩人
- Organizer
  第56回日本糖尿病学会近畿地方会
- Invited
- Data Source
  KAKENHI-PROJECT-17K09842
[Presentation] ABCC8遺伝子変異による糖尿病の臨床像の検討2019
- Author(s)
  松谷紀彦、古田浩人、松野正平、浦木進丞、宮脇正和、唐戸嶋麻衣、玉井昌紀、小宮　圭、土井麻子、森田修平、有安宏之、岩倉　浩、西　理宏、鈴木啓之、赤水尚史
- Organizer
  第62回日本糖尿病学会年次学術集会
- Data Source
  KAKENHI-PROJECT-17K09842
[Presentation] 低血糖症から糖尿病への移行が観察されたABCC8遺伝子変異による糖尿病の１家系2018
- Author(s)
  唐戸嶋　麻衣、古田浩人、松谷紀彦、松野正平、玉井昌紀、小宮　圭、土井麻子、森田修平、竹島　健、西　理宏、赤水尚史
- Organizer
  第55回日本糖尿病学会近畿地方会
- Data Source
  KAKENHI-PROJECT-17K09842
[Presentation] グルコキナーゼ遺伝子c.680 -1G>A変異によるMODY2の同定と臨床像の検討2018
- Author(s)
  松谷紀彦、古田浩人、松野正平、土井麻子、浦木進丞、古田眞智、土屋　等、有安宏之、岩倉　浩、西　理宏、赤水尚史
- Organizer
  第61回日本糖尿病学会年次学術集会
- Data Source
  KAKENHI-PROJECT-17K09842
[Presentation] ABCC8遺伝子変異による新生児糖尿病症例の５年間の臨床経過2018
- Author(s)
  古田浩人、浦木進丞、宮脇正和、松野正平、松谷紀彦、土井麻子、島　友子、西　理宏、鈴木啓之、赤水尚史、
- Organizer
  第55回日本糖尿病学会近畿地方会
- Data Source
  KAKENHI-PROJECT-17K09842
[Presentation] シンポジウム“Genomics & Beyond”「Monogenic diabetes診療の現状と未来」2017
- Author(s)
  古田浩人
- Organizer
  第67回日本体質医学会総会
- Invited
- Data Source
  KAKENHI-PROJECT-17K09842
[Presentation] シンポジウム２　糖尿病の多様性とテーラーメイド医療：病型・病態に応じた治療の最適化「その他のタイプ（単一遺伝子異常による糖尿病）」2017
- Author(s)
  古田浩人
- Organizer
  第54回日本糖尿病学会近畿地方会
- Invited
- Data Source
  KAKENHI-PROJECT-17K09842
[Presentation] ABCC8遺伝子変異による糖尿病の臨床的特長2014
- Author(s)
  古田浩人、浦木進丞、高木伴幸、土井麻子、宮脇正和、島友子、西理宏、吉川徳茂、赤水尚史
- Organizer
  第57回日本糖尿病学会年次学術集会
- Place of Presentation
  大阪市
- Year and Date
  2014-05-24
- Data Source
  KAKENHI-PROJECT-23591319
[Presentation] 遺伝子診断が治療法の決定に有用であった若年発症糖尿病の1例2013
- Author(s)
  浦木進丞、古田浩人、飯島文憲、宮脇正和、土井麻子、有安宏之、川嶋弘道、若﨑久生、西理宏、吉川徳茂、赤水尚史
- Organizer
  第50回日本糖尿病学会近畿地方会
- Place of Presentation
  京都市
- Year and Date
  2013-11-23
- Data Source
  KAKENHI-PROJECT-23591319
[Presentation] Clinical and functional characterization of the Pro1198Leu ABCC8 gene mutation associated with permanent neonatal diabetes mellitus2013
- Author(s)
  Furuta H, Takagi T, Miyawaki M, Nagashima K, Shimada T, Doi A, Matsuno S, Tanaka D, Nishi M, Sasaki H, Inagaki N, Yoshikawa N, Nanjo K, Akamizu T
- Organizer
  βCell Workshop 2013
- Place of Presentation
  Kyoto, Japan
- Data Source
  KAKENHI-PROJECT-23591319
[Presentation] 遺伝子診断後にインスリンからSU薬に治療を変更しえたABCC8遺伝子変異による新生児糖尿病の2例2013
- Author(s)
  浦木進丞、高木伴幸、古田浩人、島友子、川嶋弘道、宮脇正和、長嶋一昭、土井麻子、島田健、若﨑久生、西理宏、中尾大成、佐々木秀行、稲垣暢也、南條輝志男、赤水尚史
- Organizer
  第56回日本糖尿病学会年次学術集会
- Place of Presentation
  熊本市
- Year and Date
  2013-05-18
- Data Source
  KAKENHI-PROJECT-23591319
[Presentation] 遺伝子診断後にインスリンからSU薬に治療を変更しえたABCC8遺伝子変異による新生児糖尿病の２例．2013
- Author(s)
  浦木進丞、高木伴幸、古田浩人、島　友子、川嶋弘道、宮脇正和、長嶋一昭、土井麻子、島田　健、若﨑久生、西　理宏、中尾大成、佐々木秀行、稲垣暢也、南條輝志男、赤水尚史
- Organizer
  第56回日本糖尿病学会年次学術集会
- Place of Presentation
  熊本市
- Data Source
  KAKENHI-PROJECT-23591319
[Presentation] Regulation of AMP-activated protein kinase alpha 2 expression by a fasting/ghrelin-induced transcription factor, AF5q31, in the hypothalamic neurons2012
- Author(s)
  Komori T, Doi A, Nosaka T, Furuta H, Akamizu T, Kitamura T, Senba E, Morikawa Y
- Organizer
  The 48th EASD Annual Meeting 2012.10.2
- Place of Presentation
  Berlin, Germany
- Year and Date
  2012-10-02
- Data Source
  KAKENHI-PROJECT-23659385
[Presentation] Genetic Prediction of Type 2 Diabetes2012
- Author(s)
  Furuta, H
- Organizer
  9th IDF-WPR Congress & 4th AASD Scientific Meeting
- Place of Presentation
  Kyoto, Japan
- Data Source
  KAKENHI-PROJECT-23591319
[Presentation] 視床下部神経細胞でのAMPKシグナル活性化における転写因子AFF4の役割2012
- Author(s)
  小森忠祐、土井麻子、古田浩人、赤水尚史、森川吉博
- Organizer
  第24回分子糖尿病学シンポジウム
- Place of Presentation
  東京
- Year and Date
  2012-12-08
- Data Source
  KAKENHI-PROJECT-23659385
[Presentation] 2型糖尿病疾患感受性遺伝子多型とグルカゴンによるインスリン分泌との関係2011
- Author(s)
  古田浩人、松野正平, 古川安志, 土井麻子, 西理宏, 佐々木秀行, 三家登喜夫, 南條輝志男, 赤水尚史
- Organizer
  第54回日本糖尿病学会年次学術総会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-23591319
[Presentation] 学童検診での尿糖陽性が診断の契機となったMODY2の1家系2011
- Author(s)
  1.遠藤久子、古田浩人、松野正平、土井麻子、高木伴幸、西理宏, 佐々木秀行, 南條輝志男, 赤水尚史
- Organizer
  第48回日本糖尿病学会近畿地方会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-23591319
[Presentation] シンポジウム「2 型糖尿病関連遺伝子はどこまで解明されたか」、TCF7L2 遺伝子多型による2 型糖尿病発症リスク増加機序の検討2009
- Author(s)
  古田浩人
- Organizer
  第52 回日本糖尿病学会年次学術集会
- Place of Presentation
  大阪
- Year and Date
  2009-05-22
- Data Source
  KAKENHI-PROJECT-19591064
[Presentation] TCF7L2 遺伝子多型による2 型糖尿病発症リスク増加機序の検討2008
- Author(s)
  古田浩人
- Organizer
  第20 回分子糖尿病学シンポジウム
- Place of Presentation
  東京
- Year and Date
  2008-12-13
- Data Source
  KAKENHI-PROJECT-19591064
[Presentation] TCF7L2遺伝子多型による2型糖尿病発症リスク増加機序の検討2008
- Author(s)
  古田浩人
- Organizer
  第20回分子糖尿病学シンポジウム
- Place of Presentation
  東京コンファレンスセンター品川
- Year and Date
  2008-12-13
- Data Source
  KAKENHI-PROJECT-19591064
[Presentation] Polymorphisms in the TCF7L2 gene are associated with impaired insulin secretion in Japanese type 2 diabetic patients2007
- Author(s)
  Hiroto Furuta, et. al.
- Organizer
  14^<th> Japan-Korea symposium on diabetes mellitus
- Place of Presentation
  Kyoto,Japan
- Year and Date
  2007-10-06
- Data Source
  KAKENHI-PROJECT-19591064
[Presentation] 遺伝子診断が治療法の決定に有用であった若年発症糖尿病の１例
- Author(s)
  浦木進丞、古田浩人、飯島文憲、宮脇正和、土井麻子、有安宏之、川嶋弘道、若﨑久生、西　理宏、吉川徳茂、赤水尚史
- Organizer
  第50回日本糖尿病学会近畿地方会
- Place of Presentation
  京都市
- Data Source
  KAKENHI-PROJECT-23591319

1. MORIKAWA Yoshihiro (60230108)

# of Collaborated Projects: 4 results

# of Collaborated Products: 4 results
2. KOMORI Tadasuke (90433359)

# of Collaborated Projects: 3 results

# of Collaborated Products: 4 results
3. NANJO Kishio (40164511)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
4. NISHI Masahiro (90228148)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
5. HISAOKA TOMOKO (00398463)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
6. MIYAJIMA ATSUSHI (50135232)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
7. KITAMURA TOSHIO (20282527)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
8. 森田修平 (50372868)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
9. GYOBU HIROAKI

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. TANAKA Minoru

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
11. MISHIMA Hiroyuki

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
12. SHIMA Yuko

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
13. 吉浦孝一郎

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
14. 野阪哲哉

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

FURUTA HIROTO 古田 浩人

FURUTA Hiroto 古田 浩人

古田 浩人 フルタ ヒロト

Research Projects

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Co-Researchers

若年発症糖尿病濃厚家系の原因遺伝子探索と診療への応用Principal Investigator

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Elucidation of causal genes of monogenic diabetes and it applies to the medical treatmentPrincipal Investigator

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Role of exercise-induced oncostatin M in the treatment of NASH

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Roles of AFF4, a member of the AF4 family of transcription factors, in FGF21 resistance

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Search for novel MODY genes with exome sequencingPrincipal Investigator

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Functional roles of AF5q31and its relationship with anorexia nervosa.

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Mechanism of increased risk of type 2 diabetes by TCF7L2 gene polymorphismsPrincipal Investigator

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The Investigation of Genetic Factors Involved in the Pathogeneses and Pathophysiology of Obese Type 2 Diabetes

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2型糖尿病患者におけるインスリン抵抗性に関与する遺伝的要因の解析

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[Book] 「すべてがわかる最新・糖尿病」、編集 門脇孝、2011

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[Journal Article] A family in which people with a heterozygous ABCC8 gene mutation (p.Lys1385Gln) have progressed from hyperinsulinemic hypoglycemia to hyperglycemia2020

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[Journal Article] Identification of a compound heterozygous inactivating ABCC8 gene mutation responsible for young-onset diabetes with exome sequencing2020

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[Journal Article] 全容が解き明かされつつある糖尿病遺伝素因ー若年発症糖尿病 MODY1-6以外の病因と病態についてー2020

Author(s)

Journal Title

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[Journal Article] Neonatal diabetes caused by the heterozygous Pro1198Leu mutation in the ABCC8 gene in a male infant: 6-year clinical course2020

FURUTA HIROTO 古田浩人

FURUTA Hiroto 古田浩人

古田浩人フルタヒロト

[Book] 「すべてがわかる最新・糖尿病」、編集　門脇孝、2011

[Journal Article] 全容が解き明かされつつある糖尿病遺伝素因ー若年発症糖尿病　MODY1-6以外の病因と病態についてー2020