YAGASAKI Hideaki 矢ヶ崎英晃

… Alternative Names

矢ヶ崎英晃ヤガサキヒデアキ

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Researcher Number	00377540
Other IDs
Affiliation (Current)	2025: 山梨大学, 大学院総合研究部, 特任准教授
Affiliation (based on the past Project Information) *help	2022 – 2023: 山梨大学, 大学院総合研究部, 特任准教授 2021 – 2022: 山梨大学, 大学院総合研究部, 特任講師 2020: 山梨大学, 大学院総合研究部, 講師 2014: 山梨大学, 総合研究部, 助教
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related Except Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Pediatrics
Keywords	Principal Investigator 遺伝子スクリーニング / 甲状腺形成遺伝子 / 次世代シークエンサー / 遺伝子解析 / ジェノタイピング / 遺伝子 / 先天性甲状腺機能低下症 Except Principal Investigator TP53 / p53 / アンドロゲン受容体 … More / 性成熟 / 精子細胞 / 精母細胞 / セルトリ細胞 / Smad / 精毋細胞 / 抗ミュラー管ホルモン受容体 / 精子形成 / 精巣 / 生殖細胞 / 抗ミュラー管ホルモン Less

Novel molecular screening system for thyroid embryologic genesPrincipal Investigator
- Principal Investigator
  
  矢ヶ崎英晃
- Project Period (FY)
  2020 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  University of Yamanashi
Elucidation of the mechanism of hyperactivation of p53 lacking C terminal domain
- Principal Investigator
  
  Nakane Takaya
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  University of Yamanashi
Effect of anti-Mullerian hormone on germ cells of maturing rat testis
- Principal Investigator
  
  KENJI Ohyama
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  University of Yamanashi

All 2023 2022 2021 2020

All Journal Article Presentation Book

[Book] 小児科診療　Vol.86　No.11　「正常と異常な成長の“見極め”」2023
- Author(s)
  矢ヶ崎　英晃
- Total Pages
  1321
- Publisher
  診断と治療社
- Data Source
  KAKENHI-PROJECT-20K08154
[Book] BIO Clinica　先天性甲状腺機能低下症における遺伝子解析スクリーニングシステムの構築2022
- Author(s)
  渡邊大輔、矢ヶ崎英晃
- Total Pages
  5
- Publisher
  北隆館
- Data Source
  KAKENHI-PROJECT-20K08154
[Journal Article] Psychological distress among early medical residents: A 2-year longitudinal cohort study over seven years in Japan2023
- Author(s)
  Watanabe Shintaro、Uemura Takuji、Iwata Yusuke、Yagasaki Hideaki、Itakura Jun、Suzuki Takefumi
- Journal Title
  
  Comprehensive Psychiatry
  
  Volume: 127 Pages: 152425-152425
- DOI
  10.1016/j.comppsych.2023.152425
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K08154
[Journal Article] Eighteen-years follow-up of congenital hypothyroidism by TSHR gene p.Arg109Gln and p.Arg450His variants2023
- Author(s)
  Watanabe D, Yagasaki H, Mitsui Y, Inukai T
- Journal Title
  
  Nagoya Journal of Medical Science
  
  Volume: 85 Issue: 2 Pages: 369-374
- DOI
  10.18999/nagjms.85.2.369
- ISSN
  0027-7622
- URL
  https://nagoya.repo.nii.ac.jp/records/2006276
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K08154
[Journal Article] Novel TRPS1 frameshift variant in tricho-rhino-phalangeal syndrome type I accompanied by zinc deficiency2023
- Author(s)
  Yagasaki Hideaki、Narusawa Hiromune、Watanabe Daisuke、Kobayashi Koji、Mitsui Hiroshi、Asano Yoshihiro、Nagata Miho、Yonei Ayumi、Inukai Takeshi
- Journal Title
  
  European Journal of Medical Genetics
  
  Volume: 66 Issue: 12 Pages: 104870-104870
- DOI
  10.1016/j.ejmg.2023.104870
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K08154
[Journal Article] Compound heterozygous variants of the NARS2 gene in siblings with developmental delay, epilepsy, and neonatal diabetes syndrome2022
- Author(s)
  Yagasaki Hideaki、Sano Fumikazu、Narusawa Hiromune、Watanabe Daisuke、Kaga Yoshimi、Kobayashi Koji、Asano Yoshihiro、Nagata Miho、Yonei Ayumi、Inukai Takeshi
- Journal Title
  
  American Journal of Medical Genetics Part A
  
  Volume: 188 Issue: 8 Pages: 2466-2471
- DOI
  10.1002/ajmg.a.62873
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K08154, KAKENHI-PROJECT-23K24328
[Journal Article] Idiopathic central precocious puberty with Prader Willi syndrome: pubertal development with discontinuation of gonadotropin-releasing hormone analog2022
- Author(s)
  Kobayashi Mami、Yagasaki Hideaki、Tamaru Kei、Mitsui Yumiko、Inukai Takeshi
- Journal Title
  
  Endocrinology, Diabetes & Metabolism Case Reports
  
  Volume: 2022 Pages: 22-0244
- DOI
  10.1530/edm-22-0244
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K08154
[Journal Article] Screening of frequent variants associated with congenital hypothyroidism: a comparison with next generation sequencing2021
- Author(s)
  Watanabe Daisuke、Yagasaki Hideaki、Narusawa Hiromune、Saito Tomohiro、Mitsui Yumiko、Miyake Kunio、Ohta Masanori、Inukai Takeshi
- Journal Title
  
  Endocr J
  
  Volume: 68 Issue: 12 Pages: 1411-1419
- DOI
  10.1507/endocrj.EJ21-0353
- NAID
  130008136503
- ISSN
  0918-8959, 1348-4540
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K21707, KAKENHI-PROJECT-20H03928, KAKENHI-PROJECT-20K08154
[Journal Article] A novel c.1391_1428delinsT mutation in TSHR as a cause of familial congenital hypothyroidism with delayed onset2021
- Author(s)
  Watanabe Daisuke、Yagasaki Hideaki、Ishii Sayaka、Mitsui Yumiko、Nakane Takaya、Inukai Takeshi
- Journal Title
  
  Pediatrics And Neonatology
  
  Volume: 61 Issue: 1 Pages: 114-116
- DOI
  10.1016/j.pedneo.2019.11.003
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K08154
[Presentation] バセドウ病を発症した 46, XX, der(3)t(3:8) (p26;q24.23) の幼児例 Grave’s disease in an infant with molecularly confirmed 46, XX, der(3)t(3:8)(p26;q24.23)2023
- Author(s)
  矢ヶ崎英晃、成澤宏宗、渡邊大輔、牧野耕一、佐藤和正、佐野友昭、小林浩司、加賀佳美、太田正法、犬飼岳史
- Organizer
  第56回日本小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-20K08154
[Presentation] Narrowing down the A/B-DMR methylation maintenance region based on a deletion in familial Pseudohypoparathyroidism 12023
- Author(s)
  Hiromune Narusawa, Yukie Nakagawa, Sayaka Isobe, Kyoichiro Tsuchiya, Hideaki Yagasaki, Kazuhiko Nakabayashi, Maki Fukami, Masayo Kagami
- Organizer
  68th Annual Meeting of the Japan Society of Human Genetics (JSHG)
- Data Source
  KAKENHI-PROJECT-20K08154
[Presentation] GNAS 欠失 Pseudohypoparathyroidism 1A 例の全ゲノムメチル化解析による A/B-DMR メチル化維維持必須領域限局化2023
- Author(s)
  成澤宏宗、中川由季絵、磯部さやか、土屋恭一郎、矢ケ崎英晃、中林一彦、深見真紀、鏡雅代
- Organizer
  第56回日本小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-20K08154
[Presentation] 成長障害および発達遅滞を伴う 16p13.11 微小重複の女児例2023
- Author(s)
  渡邊大輔、矢ヶ崎英晃、成澤宏宗、犬飼岳史
- Organizer
  第56回日本小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-20K08154
[Presentation] 16p13.11 microduplication with growth retardation and developmental disorders2023
- Author(s)
  Daisuke Watanabe, Hideaki Yagasaki, Hiromune Narusawa, Takeshi Inukai
- Organizer
  68th Annual Meeting of the Japan Society of Human Genetics (JSHG)
- Data Source
  KAKENHI-PROJECT-20K08154
[Presentation] 先天性甲状腺機能低下症における遺伝子解析スクリーニング2020
- Author(s)
  渡邊大輔　成澤宏宗　矢ヶ崎英晃　　牧野耕一　佐藤和正　佐野友昭　小林浩司　中根貴弥　太田正法　犬飼岳史
- Organizer
  第52回日本小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-20K08154
[Presentation] TSHR遺伝子に新規c.1391_1428delinsT変異を認めた、先天性甲状腺機能低下症家系2020
- Author(s)
  渡邊大輔、矢ヶ崎英晃、成澤宏宗、牧野耕一、石井佐綾香、三井弓子、中根貴弥、杉田完爾
- Organizer
  第121回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-20K08154

1. KENJI Ohyama (80051861)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
2. OHTA Masanori (80233146)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
3. SANO Tomoaki (80447705)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. Nakane Takaya (90422683)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. 成澤宏宗 (70808013)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

YAGASAKI Hideaki 矢ヶ崎 英晃

矢ヶ崎 英晃 ヤガサキ ヒデアキ

Research Projects

Research Products

Co-Researchers

Novel molecular screening system for thyroid embryologic genesPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Elucidation of the mechanism of hyperactivation of p53 lacking C terminal domain

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Effect of anti-Mullerian hormone on germ cells of maturing rat testis

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Book] 小児科診療 Vol.86 No.11 「正常と異常な成長の“見極め”」2023

Author(s)

Total Pages

Publisher

Data Source

[Book] BIO Clinica 先天性甲状腺機能低下症における遺伝子解析スクリーニングシステムの構築2022

Author(s)

Total Pages

Publisher

Data Source

[Journal Article] Psychological distress among early medical residents: A 2-year longitudinal cohort study over seven years in Japan2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Eighteen-years follow-up of congenital hypothyroidism by TSHR gene p.Arg109Gln and p.Arg450His variants2023

Author(s)

Journal Title

DOI

ISSN

URL

Language

Data Source

[Journal Article] Novel TRPS1 frameshift variant in tricho-rhino-phalangeal syndrome type I accompanied by zinc deficiency2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Compound heterozygous variants of the NARS2 gene in siblings with developmental delay, epilepsy, and neonatal diabetes syndrome2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Idiopathic central precocious puberty with Prader Willi syndrome: pubertal development with discontinuation of gonadotropin-releasing hormone analog2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Screening of frequent variants associated with congenital hypothyroidism: a comparison with next generation sequencing2021

Author(s)

Journal Title

DOI

NAID

ISSN

Language

Data Source

[Journal Article] A novel c.1391_1428delinsT mutation in TSHR as a cause of familial congenital hypothyroidism with delayed onset2021

Author(s)

Journal Title

DOI

Data Source

[Presentation] バセドウ病を発症した 46, XX, der(3)t(3:8) (p26;q24.23) の幼児例 Grave’s disease in an infant with molecularly confirmed 46, XX, der(3)t(3:8)(p26;q24.23)2023

Author(s)

Organizer

Data Source

[Presentation] Narrowing down the A/B-DMR methylation maintenance region based on a deletion in familial Pseudohypoparathyroidism 12023

Author(s)

YAGASAKI Hideaki 矢ヶ崎英晃

矢ヶ崎英晃ヤガサキヒデアキ

[Book] 小児科診療　Vol.86　No.11　「正常と異常な成長の“見極め”」2023

[Book] BIO Clinica　先天性甲状腺機能低下症における遺伝子解析スクリーニングシステムの構築2022

[Presentation] GNAS 欠失 Pseudohypoparathyroidism 1A 例の全ゲノムメチル化解析による A/B-DMR メチル化維維持必須領域限局化2023

[Presentation] 成長障害および発達遅滞を伴う 16p13.11 微小重複の女児例2023