KIDA MIYUKI 貴田みゆき

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KIDA Miyuki 貴田みゆき

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Researcher Number	80507442
Affiliation (based on the past Project Information) *help	2015: 北海道大学, 医学(系)研究科(研究院), 客員研究員 2014: 北海道大学, 医学(系)研究科(研究院), その他 2013: 北海道大学, 医学(系)生殖・発達医学研究科(研究院), 客員研究員 2011 – 2013: 北海道大学, 医学(系)研究科(研究院), 客員研究員 2008 – 2009: Hokkaido University, 大学院・医学研究科, 客員研究員
Review Section/Research Field	Principal Investigator Orthodontic/Pediatric dentistry / Orthodontics/Pediatric dentistry
Keywords	Principal Investigator 遺伝子解析 / 口腔遺伝性疾患 / 網羅的解析 / 遺伝性多数歯欠損症 / 多数歯欠損症 / 遺伝性非症候性多数歯欠損症 / 発症前診断 / 診断 / エナメル基質タンパク / ヒトエナメルマトリックス蛋白 / 遺伝性象牙質形成不全症 / 遺伝性エナメル質形成不全症

Research Projects
(3 results)
Research Products
(11 results)

Exhaustive analysis of nonsyndoromic Oligodoitia in multiple Japanese familiesPrincipal Investigator
- Principal Investigator
  
  KIDA MIYUKI
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Orthodontics/Pediatric dentistry
- Research Institution
  Hokkaido University
Exhaustive analysis of oral genetic disease and oligodontiaPrincipal Investigator
- Principal Investigator
  
  KIDA MIYUKI
- Project Period (FY)
  2011 – 2012
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Orthodontic/Pediatric dentistry
- Research Institution
  Hokkaido University
The study of molecular genetics for oral genetic disorder and clinical application about human enamel matrixPrincipal Investigator
- Principal Investigator
  
  KIDA Miyuki
- Project Period (FY)
  2008 – 2009
- Research Category
  
  Grant-in-Aid for Young Scientists (Start-up)
- Research Field
  
  Orthodontic/Pediatric dentistry
- Research Institution
  Hokkaido University

All 2015 2011 2009 2008 Other

All Journal Article Presentation

[Journal Article] Outcomes in two Japanese adenosine deaminase-deficiency patients treated by stem cell gene therapy with no cytoreductive conditioning.2015
- Author(s)
  Otsu M, Yamada M, Nakajima S, Kida M, Maeyama Y, Hatano N, Toita N, Takezaki S, Okura Y, Kobayashi R, Matsumoto Y, Tatsuzawa O, Tsuchida F, Kato S, Kitagawa M, Mineno J, Hershfield MS, Bali P, Candotti F, Onodera M, Kawamura N, Sakiyama Y, Ariga T.
- Journal Title
  
  Journal of Clinical Immunology
  
  Volume: 35(4) Issue: 4 Pages: 384-398
- DOI
  10.1007/s10875-015-0157-1
- NAID
  120005752845
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25861996
[Journal Article] Identification of the DSPP mutation in a new kindred and phenotype-genotype correlation.2011
- Author(s)
  6) S-K Lee, K-E Lee, Y-H Hwang, M Kida, T Tsutsumi, T Ariga, J-C Park, J-W Kim
- Journal Title
  
  Oral Diseases
  
  Volume: Vol17(3) Issue: 3 Pages: 314-319
- DOI
  10.1111/j.1601-0825.2010.01760.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23792406
[Journal Article] Novel compound heterozygous mutations in the C3 gene : hereditary C3 deficiency2011
- Author(s)
  Yuka Okura, Masafumi Yamada, Shunichiro Takezaki, Mitsuru Nawate, Yutaka Takahashi, Miyuki Kida, Nobuaki Kawamura, Tadashi Ariga
- Journal Title
  
  Pediatrics International
  
  Volume: Volume 53(2) Pages: 16-19
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23792406
[Journal Article] Identification of the DSPP mutation in a new kindred and phenotype-genotype correlation2011
- Author(s)
  Sook-Kyung Lee, Kyung-Eun Lee, Yun-Hee Hwang, Miyuki Kida, Tomonori Tsutsumi, Tadashi Ariga, Joo-Cheol Park, Jung-Wook Kim
- Journal Title
  
  Oral Diseases
  
  Volume: 17 Pages: 314-319
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23792406
[Journal Article] De novo mutation in the DSPP gene associated with dentinogenesis imperfecta type II in a Japanese family2009
- Author(s)
  Miyuki Kida, Tomonori Tsutsumi, Masanobu Shindoh, H Ikeda, Tadashi Ariga
- Journal Title
  
  European journal of Oral Science 117
  
  Pages: 691-694
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20890009
[Journal Article] De novo mutation in the DSPP gene associated with dentinogenesis imperfecta type II in a Japanese family2009
- Author(s)
  Miuki Kida, et al
- Journal Title
  
  European Journal of Oral Sciences 117(6)
  
  Pages: 691-694
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20890009
[Journal Article] The first confirmed case with C3 deficiency caused by compound hetero zygous mutations in the C3 gene ; a new aspect of pathogenesis for C3 deficiency2008
- Author(s)
  Miuki Kida, et.al.
- Journal Title
  
  Blood Cells, Molecules, and Diseases 40
  
  Pages: 410-413
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20890009
[Journal Article] The first confirmed case with C3 deficiency caused by compound heterozygous mutations in the C3 gene; a new aspect of pathogenesis for C3 deficiency2008
- Author(s)
  Miyuki Kida, Hirotaka Fujioka, Yoshiyuki Kosaka, Kouhei Hayashi, Yukio Sakiyama, Tadashi Ariga.
- Journal Title
  
  Blood Cells, Molecules and Diseases 40
  
  Pages: 410-413
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20890009
[Presentation] A novel PAX9 mutation caused oligodontia in a Japanese family2011
- Author(s)
  Miyuki Kida, Takashi Kikuiri, Tadashi Ariga
- Organizer
  The 12th International Congress of Human Genetics Montreal
- Place of Presentation
  Canada
- Data Source
  KAKENHI-PROJECT-23792406
[Presentation] A novel PAX9 mutation caused oligodontia in a Japanese family2011
- Author(s)
  Miyuki Kida, Takashi Kikuiri, Tadashi Ariga
- Organizer
  The 12th International Congress of Human Genetics
- Place of Presentation
  palais des congres de Montreal (Canada)
- Data Source
  KAKENHI-PROJECT-23792406
[Presentation] 遺伝性を疑う非症候性多数歯欠損症例におけるPAX9 / MSX1解析
- Author(s)
  関（貴田）みゆき
- Organizer
  第52回　日本小児歯科学会大会
- Place of Presentation
  品川区立総合区民会館（東京都・品川区）
- Year and Date
  2014-05-16 – 2014-05-17
- Data Source
  KAKENHI-PROJECT-25861996

KIDA MIYUKI 貴田 みゆき

KIDA Miyuki 貴田 みゆき

Research Projects

Research Products

Exhaustive analysis of nonsyndoromic Oligodoitia in multiple Japanese familiesPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Exhaustive analysis of oral genetic disease and oligodontiaPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

The study of molecular genetics for oral genetic disorder and clinical application about human enamel matrixPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Outcomes in two Japanese adenosine deaminase-deficiency patients treated by stem cell gene therapy with no cytoreductive conditioning.2015

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] Identification of the DSPP mutation in a new kindred and phenotype-genotype correlation.2011

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Novel compound heterozygous mutations in the C3 gene : hereditary C3 deficiency2011

Author(s)

Journal Title

Data Source

[Journal Article] Identification of the DSPP mutation in a new kindred and phenotype-genotype correlation2011

Author(s)

Journal Title

Data Source

[Journal Article] De novo mutation in the DSPP gene associated with dentinogenesis imperfecta type II in a Japanese family2009

Author(s)

Journal Title

Data Source

[Journal Article] De novo mutation in the DSPP gene associated with dentinogenesis imperfecta type II in a Japanese family2009

Author(s)

Journal Title

Data Source

[Journal Article] The first confirmed case with C3 deficiency caused by compound hetero zygous mutations in the C3 gene ; a new aspect of pathogenesis for C3 deficiency2008

Author(s)

Journal Title

Data Source

[Journal Article] The first confirmed case with C3 deficiency caused by compound heterozygous mutations in the C3 gene; a new aspect of pathogenesis for C3 deficiency2008

Author(s)

Journal Title

Data Source

[Presentation] A novel PAX9 mutation caused oligodontia in a Japanese family2011

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] A novel PAX9 mutation caused oligodontia in a Japanese family2011

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] 遺伝性を疑う非症候性多数歯欠損症例におけるPAX9 / MSX1解析

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

KIDA MIYUKI 貴田みゆき

KIDA Miyuki 貴田みゆき