DATEKI Sumito 伊達木澄人

… Alternative Names

伊達木澄人ダテキスミト

Dateki Sumito 伊達木澄人

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Researcher Number	70462801
Other IDs
External Links
Affiliation (Current)	2025: 長崎大学, 医歯薬学総合研究科(医学系), 准教授
Affiliation (based on the past Project Information) *help	2023: 長崎大学, 医歯薬学総合研究科(医学系), 准教授 2017 – 2021: 長崎大学, 医歯薬学総合研究科(医学系), 准教授 2014 – 2015: 長崎大学, 病院(医学系), 助教 2013: 長崎大学, 大学病院, 助教 2010 – 2011: 独立行政法人国立成育医療研究センター, 分子内分泌研究部, 共同研究員 2009: 国立成育医療センター(研究所), 小児思春期発育研究部, 共同研究員 2009: National Research Institute for Child Health and Development, 小児思春期発育研究部, 共同研究員
Review Section/Research Field	Principal Investigator Pediatrics / Basic Section 52050:Embryonic medicine and pediatrics-related Except Principal Investigator Endocrinology
Keywords	Principal Investigator 下垂体 / ROBO1 / 脳梁低形成 / 軸索誘導 / 全エクソーム解析 / 斜視 / 先天性下垂体機能低下症 / 黄色腫 / 高シトステロール血症 / 高コレステロール血症 / 小児内分泌学 / 転写因子 / 遺伝子 … More Except Principal Investigator … More 先天性中枢性性線機能異常症 / 先天性中枢性性腺機能異常症 / 成人不妊 / 遺伝的異質性 / WAVEシステム / 少子化対策 / 標準的遺伝子診断法 / 遺伝子診断システム / DHPLC法 / 成人不妊症 Less

Clinical and genetic analyses in patients with ROBO1 mutationsPrincipal Investigator
- Principal Investigator
  
  伊達木澄人
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Nagasaki University
Genetic and Clinical analyses in patients with sitosterolemiaPrincipal Investigator
- Principal Investigator
  
  Dateki Sumito
- Project Period (FY)
  2017 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Nagasaki University
trio whole exome sequencing in patients with combined pituitary hormone deficiencyPrincipal Investigator
- Principal Investigator
  
  DATEKI Sumito
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Nagasaki University
Elucidation of the pathogenic mechanism for the hypogonadotropic hypogonadism and the development of the standard mutation analyses system in congenital hypogonadotropic hypogonadism.
- Principal Investigator
  
  SATO Naoko
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Endocrinology
- Research Institution
  National Research Institute for Child Health and Development
Molecular and functional analyses of OTX2 in patients with congenital pituitary hormone deficiencyPrincipal Investigator
- Principal Investigator
  
  DATEKI Sumito
- Project Period (FY)
  2009 – 2010
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  National Research Institute for Child Health and Development

All 2023 2019 2018 2017 2010 2009

All Journal Article Presentation

[Journal Article] A case of sitosterolemia due to compound heterozygous mutations in <i>ABCG5</i>: clinical features and treatment outcomes obtained with colestimide and ezetimibe2017
- Author(s)
  Ono S, Matsuda J, Saito A, Yamamoto Y, Fujimoto W, Shimizu H, Dateki S, Ouchi K.
- Journal Title
  
  Clinical Pediatric Endocrinology
  
  Volume: 26 Issue: 1 Pages: 17-23
- DOI
  10.1297/cpe.26.17
- NAID
  130005308194
- ISSN
  0918-5739, 1347-7358
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K14465, KAKENHI-PROJECT-17K10053
[Journal Article] OTX2遺伝子異常症の臨床的、分子遺伝学的解析2010
- Author(s)
  伊達木澄人、深見真紀、室谷浩二、安達昌功、小坂喜太郎、長谷川高誠、田中弘之、田島敏広、本村克明、木下英一、森内浩幸、緒方勤
- Journal Title
  
  ホルモンと臨床 57巻
  
  Pages: 987-992
- Data Source
  KAKENHI-PROJECT-21791025
[Journal Article] A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency.2010
- Author(s)
  Ashkenazi-Hoffnung L, Lebenthal Y, Wyatt AW, Ragge NK, Dateki S, Fukami M, Ogata T, Phillip M, Gat-Yablonski G.
- Journal Title
  
  Hum Genet. 127巻
  
  Pages: 721-729
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21791025
[Journal Article] Heterozygous OTX2 mutations are associated with variable pituitary phenotype.2010
- Author(s)
  Dateki S, et al.
- Journal Title
  
  Journal of Clinical Endocrinology and Metabolism
  
  Volume: 95 Pages: 756-764
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21791025
[Journal Article] OTX2遺伝子異常症の臨床的、分子遺伝学的解析2010
- Author(s)
  伊達木澄人, 他
- Journal Title
  
  ホルモンと臨床 (In press)
- Data Source
  KAKENHI-PROJECT-21791025
[Journal Article] Heterozygous OTX2 mutations are associated with variable pituitary phenotype.2010
- Author(s)
  Dateki S, Kosaka K, Hasegawa K, Tanaka H, Azuma N, Yokoya S, Muroya K, Adachi M, Tajima T, Motomura K, Kinoshita E, Moriuchi H, Sato N, Fukami M, Ogata T.
- Journal Title
  
  J Clin Endocrinol Metab 95巻
  
  Pages: 756-764
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21791025
[Journal Article] Heterozygous OTX2 mutations are associated with variable pituitary phenotype.2010
- Author(s)
  Dateki S, et al.
- Journal Title
  
  Journal of Clinical Endocrinology and Metabohsm 95
  
  Pages: 756-764
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21791025
[Journal Article] Mutation and Gene Copy Number Analyses of Six Pituitary Transcription Factor Genes in 71 Patients with Combined Pituitary Hormone Deficiency : Identification of a Single Patient with LHX4 Deletion.2010
- Author(s)
  Dateki S, et al.
- Journal Title
  
  Journal of Clinical Endocrinology and Metabolism
  
  Volume: 95 Pages: 4043-4047
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21791025
[Journal Article] OTX2遺伝子異常症の臨床的、分子遺伝学的解析2010
- Author(s)
  伊達木澄人, 他
- Journal Title
  
  ホルモンと臨床
  
  Volume: (In press)
- Data Source
  KAKENHI-PROJECT-21791025
[Journal Article] Mutation and Gene Copy Number Analyses of Six Pituitary Transcription Factor Genes in 71 Patients with Combined Pituitary Hormone Deficiency : Identification of a Single Patient with LHX4 Deletion.2010
- Author(s)
  Dateki S, Fukami M, Uematsu A, Kaji M, Iso M, Ono M, Mizota M, Yokoya S, Motomura K, Kinoshita E, Moriuchi H, Ogata T.
- Journal Title
  
  J Clin Endocrinol Metab 95巻
  
  Pages: 4043-4047
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21791025
[Journal Article] Heterozygous OTX2 mutations are associated with variable pituitary phenotype.2010
- Author(s)
  Dateki S, Sato N, et al.
- Journal Title
  
  J Clin Endocrinol Metab
  
  Volume: 95 Pages: 756-764
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591188
[Journal Article] An immunologically anomalous but considerably bioactive growth honnoneproduced by a novel GH1 mutation (p.D116E).2009
- Author(s)
  Dateki S, et al.
- Journal Title
  
  European Journal of Endocrinology 161
  
  Pages: 301-306
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21791025
[Presentation] 先天性下垂体機能低下症の新知見2023
- Author(s)
  伊達木澄人
- Organizer
  第49回日本神経内分泌学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-23K07293
[Presentation] 早期にエゼチミブを導入した小児シトステロール血症2例の臨床経過2019
- Author(s)
  我有茉希、清水日智、伊達木澄人
- Organizer
  第122回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-17K10053
[Presentation] 早期にエゼチミブを導入した小児シトステロール血症2例の臨床経過2019
- Author(s)
  我有茉希、清水日智、伊達木澄人
- Organizer
  第92回日本内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-17K10053
[Presentation] 早期にエゼチミブを導入した小児シトステロール血症2例の臨床経過2018
- Author(s)
  我有茉希、清水日智、伊達木澄人
- Organizer
  第52回日本小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-17K10053
[Presentation] 複合型下垂体機能低下症における包括的変異・ゲノムコピー数解析2010
- Author(s)
  伊達木澄人
- Organizer
  第44回日本小児内分泌学会
- Place of Presentation
  大阪
- Year and Date
  2010-10-08
- Data Source
  KAKENHI-PROJECT-21791025
[Presentation] Mutation and Gene Copy Number Analyses of Six Pituitary Transcription Factor Genes in 71 Patients with Combined Pituitary Hormone Deficiency : Identification of a Single Patient with LHX4 Deletion.2010
- Author(s)
  Dateki S.
- Organizer
  14th International Congress of Endocrinology (ICE2010)
- Place of Presentation
  京都
- Year and Date
  2010-03-28
- Data Source
  KAKENHI-PROJECT-21791025
[Presentation] IGF1R遺伝子領域を含むヘテロ接合性欠失を認めた子宮内発育不全、成長障害の1例2010
- Author(s)
  伊達木澄人, 他
- Organizer
  第113回日本小児科学会学術集会
- Place of Presentation
  盛岡
- Year and Date
  2010-04-26
- Data Source
  KAKENHI-PROJECT-21791025
[Presentation] 複合型下垂体機能低下症における包括的変異・ゲノムコピー数解析2010
- Author(s)
  伊達木澄人
- Organizer
  第33回日本小児遺伝学会学術集会
- Place of Presentation
  盛岡
- Year and Date
  2010-04-22
- Data Source
  KAKENHI-PROJECT-21791025
[Presentation] OTX2 mutations and hypopituitarism2010
- Author(s)
  Dateki S, et al.
- Organizer
  ICE2010 satellite symposia (Pediatric Endocrinology)
- Place of Presentation
  Tokyo
- Year and Date
  2010-04-01
- Data Source
  KAKENHI-PROJECT-21791025
[Presentation] OTX2 mutations and hypopituitarism ICE2010 satellite symposia2010
- Author(s)
  Dateki S.
- Organizer
  Pediatric Endocrinology
- Place of Presentation
  東京
- Year and Date
  2010-04-01
- Data Source
  KAKENHI-PROJECT-21791025
[Presentation] OTX2異常症の臨床的、分子遺伝学的解析2009
- Author(s)
  伊達木澄人, 他
- Organizer
  第43回日本小児内分泌学会学術集会
- Place of Presentation
  宇都宮
- Year and Date
  2009-10-02
- Data Source
  KAKENHI-PROJECT-21791025
[Presentation] OTX2遺伝子異常症の臨床的および分子遺伝学的解析2009
- Author(s)
  伊達木澄人
- Organizer
  第43回日本小児内分泌学会
- Place of Presentation
  宇都宮
- Year and Date
  2009-10-01
- Data Source
  KAKENHI-PROJECT-21791025
[Presentation] Heterozygous OTX2 mutations are associated with variable pituitary hormone deficiency2009
- Author(s)
  Dateki S, et al.
- Organizer
  The 8th Join Meeting ESPE-LWPES
- Place of Presentation
  NEW YORK
- Year and Date
  2009-09-09
- Data Source
  KAKENHI-PROJECT-21791025
[Presentation] 無・小眼球症責任遺伝子OTX2は下垂体発生・分化に関与する2009
- Author(s)
  伊達木澄人
- Organizer
  第82回日本内分泌学会学術総会
- Place of Presentation
  群馬
- Year and Date
  2009-04-22
- Data Source
  KAKENHI-PROJECT-21791025
[Presentation] Heterozygous OTX2 mutations are associated with variable pituitary hormone deficiency.2009
- Author(s)
  Dateki S.
- Organizer
  The 8th Joint meeting, ESPE-LWPES in association with APEG, APPES, SLEP, JSPE.
- Place of Presentation
  New York
- Year and Date
  2009-09-10
- Data Source
  KAKENHI-PROJECT-21791025
[Presentation] OTX2異常症の臨床的、分子遺伝学的解析2009
- Author(s)
  伊達木澄人, 他
- Organizer
  第54回日本人類遺伝学会
- Place of Presentation
  東京
- Year and Date
  2009-09-24
- Data Source
  KAKENHI-PROJECT-21791025
[Presentation] 無・小眼球症責任遺伝子OTX2は,下垂体発生・機能に関与する2009
- Author(s)
  伊達木澄人
- Organizer
  第82回日本内分泌学会
- Place of Presentation
  群馬
- Year and Date
  2009-04-23
- Data Source
  KAKENHI-PROJECT-21791025
[Presentation] OTX2遺伝子異常症の臨床的,分子遺伝学的解析2009
- Author(s)
  伊達木澄人
- Organizer
  第54回日本人類遺伝学会
- Place of Presentation
  東京
- Year and Date
  2009-09-24
- Data Source
  KAKENHI-PROJECT-21791025
[Presentation] 下垂体の発生と疾患、OTX2遺伝子異常症2009
- Author(s)
  伊達木澄人
- Organizer
  Forum on Growth Hormone Research 2009
- Place of Presentation
  東京
- Year and Date
  2009-10-17
- Data Source
  KAKENHI-PROJECT-21791025

1. SATO Naoko (10383069)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
2. WATANABE Satoshi

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

DATEKI Sumito 伊達木 澄人

伊達木 澄人 ダテキ スミト

Dateki Sumito 伊達木 澄人

Research Projects

Research Products

Co-Researchers

Clinical and genetic analyses in patients with ROBO1 mutationsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Genetic and Clinical analyses in patients with sitosterolemiaPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

trio whole exome sequencing in patients with combined pituitary hormone deficiencyPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Elucidation of the pathogenic mechanism for the hypogonadotropic hypogonadism and the development of the standard mutation analyses system in congenital hypogonadotropic hypogonadism.

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Molecular and functional analyses of OTX2 in patients with congenital pituitary hormone deficiencyPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] A case of sitosterolemia due to compound heterozygous mutations in <i>ABCG5</i>: clinical features and treatment outcomes obtained with colestimide and ezetimibe2017

Author(s)

Journal Title

DOI

NAID

ISSN

Language

Data Source

[Journal Article] OTX2遺伝子異常症の臨床的、分子遺伝学的解析2010

Author(s)

Journal Title

Data Source

[Journal Article] A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency.2010

Author(s)

Journal Title

Data Source

[Journal Article] Heterozygous OTX2 mutations are associated with variable pituitary phenotype.2010

Author(s)

Journal Title

Data Source

[Journal Article] OTX2遺伝子異常症の臨床的、分子遺伝学的解析2010

Author(s)

Journal Title

Data Source

[Journal Article] Heterozygous OTX2 mutations are associated with variable pituitary phenotype.2010

Author(s)

Journal Title

Data Source

[Journal Article] Heterozygous OTX2 mutations are associated with variable pituitary phenotype.2010

Author(s)

Journal Title

Data Source

[Journal Article] Mutation and Gene Copy Number Analyses of Six Pituitary Transcription Factor Genes in 71 Patients with Combined Pituitary Hormone Deficiency : Identification of a Single Patient with LHX4 Deletion.2010

Author(s)

Journal Title

Data Source

[Journal Article] OTX2遺伝子異常症の臨床的、分子遺伝学的解析2010

Author(s)

Journal Title

Data Source

[Journal Article] Mutation and Gene Copy Number Analyses of Six Pituitary Transcription Factor Genes in 71 Patients with Combined Pituitary Hormone Deficiency : Identification of a Single Patient with LHX4 Deletion.2010

Author(s)

Journal Title

Data Source

DATEKI Sumito 伊達木澄人

伊達木澄人ダテキスミト

Dateki Sumito 伊達木澄人