Makino Satoshi 牧野悟士

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MAKINO Satoshi 牧野悟士

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Researcher Number	30423403
Other IDs
Affiliation (Current)	2025: 東北大学, 東北メディカル・メガバンク機構, 助教
Affiliation (based on the past Project Information) *help	2017 – 2023: 東北大学, 東北メディカル・メガバンク機構, 助教 2013 – 2016: 東北大学, 東北メディカル・メガバンク機構, 研究支援者 2012: 山形大学, 医学部, 助教 2010 – 2011: 滋賀医科大学, 分子神経科学研究センター, 特任助教 2009: Shiga University of Medical Science, 分子神経科学研究センター 2008 – 2009: Shiga University of Medical Science, 分子神経科学研究センター, 非常勤研究員
Review Section/Research Field	Principal Investigator Human genetics / Basic Section 58030:Hygiene and public health-related: excluding laboratory approach
Keywords	Principal Investigator 発現制御 / 核酸 / 遺伝子 / 外れ値検出 / データクリーニング / コホート研究 / 脳・神経 / ゲノム医科学 / 末梢神経疾患 / 末梢神経 … More / ミトコンドリア / 人類遺伝学 / 神経 / 転写障害 / 神経変性 / 転写因子 Less

Automation of questionnaire data cleaning in inter-cohort collaborationPrincipal Investigator
- Principal Investigator
  
  Makino Satoshi
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 58030:Hygiene and public health-related: excluding laboratory approach
- Research Institution
  Tohoku University
Development of a new data cleaning method for questionnaires used in large cohortsPrincipal Investigator
- Principal Investigator
  
  MAKINO Satoshi
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 58030:Hygiene and public health-related: excluding laboratory approach
- Research Institution
  Tohoku University
Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in COX6A1Principal Investigator
- Principal Investigator
  
  Makino Satoshi
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Tohoku University
General transcription factor TAF1 is involved in transcriptional impairment and neurodegenerationPrincipal Investigator
- Principal Investigator
  
  MAKINO Satoshi
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Tohoku University
  Yamagata University
Neuron-Specific Function of N-TAF1, the disease causative gene of Hereditary Dystonia(DYT3)Principal Investigator
- Principal Investigator
  
  MAKINO Satoshi
- Project Period (FY)
  2010 – 2011
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Human genetics
- Research Institution
  Shiga University of Medical Science
Functional analysis of N-TAF1, the disease causative gene of X-linked recessive dystonia-parkinsonismPrincipal Investigator
- Principal Investigator
  
  MAKINO Satoshi
- Project Period (FY)
  2008 – 2009
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Human genetics
- Research Institution
  Shiga University of Medical Science

All 2020 2019 2015 2014 2013 2012 2010 2009 2008 Other

All Journal Article Presentation Other

[Journal Article] Genome-wide association study identifies new loci for albuminuria in the Japanese population2020
- Author(s)
  Hiroshi Okuda, Koji Okamoto, Michiaki Abe, Kota Ishizawa, Satoshi Makino, Osamu Tanabe, Junichi Sugawara, Atsushi Hozawa, Kozo Tanno, Makoto Sasaki, Gen Tamiya, Masayuki Yamamoto, Sadayoshi Ito, Tadashi Ishii
- Journal Title
  
  Clinical and Experimental Nephrology
  
  Volume: 印刷中 Issue: 8 Pages: 1-9
- DOI
  10.1007/s10157-020-01884-x
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K10099, KAKENHI-PUBLICLY-19H05200, KAKENHI-PROJECT-17H00840, KAKENHI-PROJECT-17K09641
[Journal Article] Outlier detection for questionnaire data in biobanks2019
- Author(s)
  Sakurai Rieko、Ueki Masao、Makino Satoshi、Hozawa Atsushi、Kuriyama Shinichi、Takai-Igarashi Takako、Kinoshita Kengo、Yamamoto Masayuki、Tamiya Gen
- Journal Title
  
  International Journal of Epidemiology
  
  Volume: 印刷中 Issue: 4 Pages: 1305-1315
- DOI
  10.1093/ije/dyz012
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K10099, KAKENHI-PROJECT-18K11420, KAKENHI-PROJECT-15K00295, KAKENHI-PROJECT-16K00064, KAKENHI-PROJECT-16K08638, KAKENHI-PUBLICLY-19H05200
[Journal Article] 3.5KJPNv2: an allele frequency panel of 3552 Japanese individuals including the X chromosome2019
- Author(s)
  Tadaka S. et al. Koshiba S. et al. Kinoshita K.（合計２５名、本研究者は１４番目）
- Journal Title
  
  Hum Genome Var
  
  Volume: 6 Issue: 1 Pages: 28-28
- DOI
  10.1038/s41439-019-0059-5
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K07298, KAKENHI-PROJECT-18K10099, KAKENHI-PUBLICLY-19H05200
[Journal Article] Waardenburg syndrome type IIE in a Japanese patient caused by a novel missense mutation in the SOX10 gene2015
- Author(s)
  Okamura K, Oiso N, Tamiya G, Makino S, Tsujioka D, Abe Y, Kawaguchi M, Hozumi Y, Shimomura Y, Suzuki T
- Journal Title
  
  J Dermatol
  
  Volume: 42 Issue: 12 Pages: 1211-1212
- DOI
  10.1111/1346-8138.13095
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K08327, KAKENHI-PROJECT-25460403
[Journal Article] Whole-exome sequencing confirmation of a novel heterozygous mutation in RUNX1 in a pregnant woman with platelet disorder.2015
- Author(s)
  Obata M, Tsutsumi S, Makino S, Takahashi K, Watanabe N, Yoshida T, Tamiya G, Kurachi H.
- Journal Title
  
  Platelets
  
  Volume: 26 Issue: 4 Pages: 364-369
- DOI
  10.3109/09537104.2014.912750
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24590400, KAKENHI-PUBLICLY-25129701, KAKENHI-PROJECT-25460403
[Journal Article] Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole exome sequencing analysis2015
- Author(s)
  Ogino D, Hashimoto T,Hattori M, Sugawara N, Akioka Y, Tamiya G, Makino S, Toyota K, Mitsui T, Hayasaka K
- Journal Title
  
  J Hum Genet
  
  Volume: 61 Issue: 2 Pages: 137-141
- DOI
  10.1038/jhg.2015.122
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K08327, KAKENHI-PROJECT-25460403
[Journal Article] A mutation of COX6A1 causes a recessive axonal or mixed form of Charcot-Marie-Tooth disease.2014
- Author(s)
  Tamiya G, Makino S, Hayashi M, Abe A, Numakura C, Ueki M, Tanaka A, Ito C, Toshimori K, Ogawa N, Terashima T, Maegawa H, Yanagisawa D, Tooyama I, Tada M, Onodera O, Hayasaka K.
- Journal Title
  
  Am J Hum Genet.
  
  Volume: 95 Issue: 3 Pages: 294-300
- DOI
  10.1016/j.ajhg.2014.07.013
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24590400, KAKENHI-PROJECT-24592441, KAKENHI-PUBLICLY-25129701, KAKENHI-PROJECT-25293041, KAKENHI-PROJECT-25460403, KAKENHI-PROJECT-25461537, KAKENHI-PROJECT-25670087, KAKENHI-PROJECT-25860842, KAKENHI-PROJECT-25870074, KAKENHI-PROJECT-26870067
[Journal Article] Visualizing Hepatic Copper Release in Long-Evans Cinnamon Rats Using Single-Photon Emission Computed Tomography.2013
- Author(s)
  Yezdimer, E.M., Umemoto, T., Yamada, H., Makino, S., Tooyama I
- Journal Title
  
  Appl. Biochem. Biotechnol
  
  Volume: 170 Issue: 5 Pages: 1138-1150
- DOI
  10.1007/s12010-013-0252-9
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-24111522, KAKENHI-PROJECT-24590400
[Journal Article] Generation of a Monoclonal Antibody Specifically Reacting with Neuron-specific TATA-Box Binding Protein-Associated Factor 1 (N-TAF1)2013
- Author(s)
  Makino S, Masuda C, Ando S, Tamiya G, Tooyama I.
- Journal Title
  
  Antibodies
  
  Volume: 2 Issue: 1 Pages: 1-8
- DOI
  10.3390/antib2010001
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590300, KAKENHI-PROJECT-24590400, KAKENHI-PUBLICLY-24112702
[Journal Article] Expression and Localization of TRK-Fused Gene Products in the Rat Brain and Retina2012
- Author(s)
  Maebayashi H, Takeuchi S, Masuda C, Makino S, Fukui K, Kimura H, Tooyama I.
- Journal Title
  
  Acta Histochem Cytochem
  
  Volume: 45巻1号 Pages: 15-23
- NAID
  130001258486
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22790332
[Journal Article] UBR5 Gene Mutation Is Associated with Familial Adult Myoclonic Epilepsy in a Japanese Family2012
- Author(s)
  Kato T, Tamiya G, Koyama S, Nakamura T, Makino S, Arawaka S, Kawanami T, Tooyama I.
- Journal Title
  
  ISRN Neurol
  
  Volume: 2012 Pages: 508308-508308
- DOI
  10.5402/2012/508308
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590300, KAKENHI-PROJECT-24590400, KAKENHI-PUBLICLY-24112702
[Journal Article] In Vivo Detection of Copper Ions by Magnetic Resonance ImagingUsing a Prion-Based Contrast Agent.2012
- Author(s)
  Makino S
- Journal Title
  
  Appl Biochem Biotechnol.
  
  Volume: 168 Issue: 3 Pages: 504-518
- DOI
  10.1007/s12010-012-9792-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22300153, KAKENHI-PROJECT-24590400
[Journal Article] Sustained expression of a neuron-specific isoform of the Taf1 gene in development stages and aging in mice2012
- Author(s)
  Jambaldorj J, Makino S, Munkhbat B, Tamiya G.
- Journal Title
  
  Biochem Biophys Res Commun
  
  Volume: 425(2) Issue: 2 Pages: 273-277
- DOI
  10.1016/j.bbrc.2012.07.081
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590300, KAKENHI-PROJECT-24590400, KAKENHI-PUBLICLY-24112702
[Journal Article] Expression and Localization of TRK-Fused Gene Products in the Rat Brain and Retina2012
- Author(s)
  Maebayashi H, Takeuchi S, Masuda C, Makino S, Fukui K, Kimura H, Tooyama I
- Journal Title
  
  ACTA HISTOCHEMICA ET CYTOCHEMICA
  
  Volume: 45 Issue: 1 Pages: 15-23
- DOI
  10.1267/ahc.11015
- NAID
  130001258486
- ISSN
  0044-5991, 1347-5800
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22790332
[Journal Article] Infiltration of T lymphocytes and expression of icam-1 in the hippocampus of patients with hippocampal sclerosis.2010
- Author(s)
  Nakahara H, Konishi Y, Beach TG, Yamada N, Makino S, Tooyama I.
- Journal Title
  
  Acta Histochem Cytochem.
  
  Volume: 46 Pages: 157-62
- NAID
  130000395320
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22790332
[Journal Article] Infiltration of T Lymphocytes and Expression of ICAM-1 in the Hippocampus of Patients with Hippocampal Sclerosis2010
- Author(s)
  Nakahara H, Konishi Y, Beach TG, Yamada N, Makino S, Tooyama I.
- Journal Title
  
  ACTA HISTOCHEMICA ET CYTOCHEMICA
  
  Volume: 43 Issue: 6 Pages: 157-162
- DOI
  10.1267/ahc.10022
- NAID
  130000395320
- ISSN
  0044-5991, 1347-5800
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22790332
[Journal Article] The mRNA Distribution of C7orf24, a Gamma-glutamyl Cyclotransferase, in Rat Tissues2009
- Author(s)
  Oda K, Makino S, Masuda C, Yoshiki T, Kitamura Y, Takata K, Yanagisawa D, Taniguchi T, Tooyama I
- Journal Title
  
  J Histochem Cytochem. 57巻12号
  
  Pages: 1121-1126
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20790266
[Journal Article] The mRNA Distribution of C7orf24, a Gamma-glutamyl Cyclotransferase, in Rat Tissues.2009
- Author(s)
  Oda K, Makino S, et al.
- Journal Title
  
  The Journal of Histochemistry & Cytochemistry 57
  
  Pages: 1121-1126
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20790266
[Presentation] Neuron-specific enhanced expression of TAF1 and its isoform2010
- Author(s)
  Makino S, Tamiya G, Tooyama I.
- Organizer
  The American Society of Human Genetics 2010 Annual Meeting
- Place of Presentation
  アメリカ合衆国・ワシントンD. C.
- Year and Date
  2010-11-05
- Data Source
  KAKENHI-PROJECT-22790332
[Presentation] Neuron specific enhanced expression of TAF1 and its isoform.2010
- Author(s)
  Satoshi Makino, Gen Tamiya, Ikuo Tooyama
- Organizer
  The American Society of Human Genetics 2010 Annual Meeting
- Place of Presentation
  アメリカ・ワシントンD.C.
- Year and Date
  2010-11-05
- Data Source
  KAKENHI-PROJECT-22790332
[Presentation] Intracellular function of neuron-specific TAF1 and its isoform in Neuro-2a mouse neuroblastoma cells2009
- Author(s)
  Makino S, Tamiya G, Tooyama I
- Organizer
  The American Society of Human Genetics 2009 Annual Meeting
- Place of Presentation
  アメリカ・ホノルル
- Year and Date
  2009-10-22
- Data Source
  KAKENHI-PROJECT-20790266
[Presentation] Intracellular function of neuron-specific TAF1 and its isoform in Neuro-2a mouse neuroblastoma cells.2009
- Author(s)
  Satoshi Makino, Gen Tamiya, Ikuo Tooyama
- Organizer
  The American Society of Human Genetics 2009 Annual Meeting
- Place of Presentation
  アメリカ・ホノルル
- Year and Date
  2009-10-22
- Data Source
  KAKENHI-PROJECT-20790266
[Presentation] Genomic Sequence Analysis of the HMSN-P region on human chromoso-me 3q132008
- Author(s)
  Makino S, Maeda K, Jamiyansuren J, Yasuno K, Kaji R, Tamiya G.
- Organizer
  The American Society of Human Genetics 2008 Annual Meeting
- Place of Presentation
  アメリカ・フィラデルフィア
- Year and Date
  2008-11-13
- Data Source
  KAKENHI-PROJECT-20790266
[]

1. 田宮元 (10317745)

# of Collaborated Projects: 3 results

# of Collaborated Products: 7 results
2. TOOYAMA Ikuo (20207533)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
3. 櫻井利恵子 (50794541)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
4. 小柴生造

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Makino Satoshi 牧野 悟士

MAKINO Satoshi 牧野 悟士

Research Projects

Research Products

Co-Researchers

Automation of questionnaire data cleaning in inter-cohort collaborationPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Development of a new data cleaning method for questionnaires used in large cohortsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in COX6A1Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

General transcription factor TAF1 is involved in transcriptional impairment and neurodegenerationPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Neuron-Specific Function of N-TAF1, the disease causative gene of Hereditary Dystonia(DYT3)Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Functional analysis of N-TAF1, the disease causative gene of X-linked recessive dystonia-parkinsonismPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Genome-wide association study identifies new loci for albuminuria in the Japanese population2020

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Outlier detection for questionnaire data in biobanks2019

Author(s)

Journal Title

DOI

Data Source

[Journal Article] 3.5KJPNv2: an allele frequency panel of 3552 Japanese individuals including the X chromosome2019

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Waardenburg syndrome type IIE in a Japanese patient caused by a novel missense mutation in the SOX10 gene2015

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Whole-exome sequencing confirmation of a novel heterozygous mutation in RUNX1 in a pregnant woman with platelet disorder.2015

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole exome sequencing analysis2015

Author(s)

Journal Title

DOI

Data Source

[Journal Article] A mutation of COX6A1 causes a recessive axonal or mixed form of Charcot-Marie-Tooth disease.2014

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Visualizing Hepatic Copper Release in Long-Evans Cinnamon Rats Using Single-Photon Emission Computed Tomography.2013

Author(s)

Journal Title

DOI

Makino Satoshi 牧野悟士

MAKINO Satoshi 牧野悟士