YASHIMA Takatoshi 八島隆敏

… Alternative Names

八島隆俊ヤシマタカトシ

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Researcher Number	50372438
External Links
Affiliation (based on the past Project Information) *help	2008: 東京医科歯科大学, 医学部付属病院, 助教 2004 – 2006: 東京医科歯科大学, 医学部附属病院, 助手 2004: Tokyo Medical and Dental University, Dept of Otolaryngology Faculty, 医学部付属病院, 助手
Review Section/Research Field	Principal Investigator Otorhinolaryngology Except Principal Investigator Otorhinolaryngology / Otorhinolaryngology / Biological Sciences
Keywords	Principal Investigator 遺伝子解析 / 皿型感音難聴 / 非症候群性感音難聴 Except Principal Investigator 脳・神経 / ゲノム / 遺伝子 / 神経科学 / バイオテクノロジー / 細胞・組織 / 脳神経疾患 … More / Cranial Nerve / Brain・Nerve / Neurology / Genome / Gene / protein / Scaffold / Six1 / Scaffold protein / 転写因子 / 内耳奇形マウス / ホメオボックス遺伝子 / 難聴 / 神経科 Less

CDH23 mutation in deaf patients and experimental animals
- Principal Investigator
  
  KITAMURA Ken
- Project Period (FY)
  2005 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Tokyo Medical and Dental University
難聴遺伝子解析による内耳聴覚・前庭の分子機構
- Principal Investigator
  
  KITAMURA Ken
- Project Period (FY)
  2004
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Tokyo Medical and Dental University
ヒト側頭骨病理標本からレーザーキャプチャー・ダイセクションによる難聴遺伝子の抽出
- Principal Investigator
  
  喜多村健
- Project Period (FY)
  2004 – 2006
- Research Category
  
  Grant-in-Aid for Exploratory Research
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Tokyo Medical and Dental University
皿型感音難聴を呈する非症候群性遺伝性難聴における難聴遺伝子の同定Principal Investigator
- Principal Investigator
  
  八島隆敏
- Project Period (FY)
  2004 – 2006
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Tokyo Medical and Dental University
Analysis of deafness using homeobox and molecular motor gene, and knockout mouse
- Principal Investigator
  
  KITAMURA Ken
- Project Period (FY)
  2002 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Tokyo Medical and Dental University

All 2005 2004 2003 Other

All Journal Article

[Journal Article] A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss2005
- Author(s)
  Noguchi Y, Yashima T, Hatanaka A, Uzawa M, Yasunami M, Kimura A, Kitamura K
- Journal Title
  
  Acta Otolaryngol 125
  
  Pages: 1189-1194
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17390457
[Journal Article] A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss.2005
- Author(s)
  Noguchi Y, Yashima T, Hatanaka A, Uzawa M, Yasunami M, Kimura A, Kitamura K
- Journal Title
  
  Acta Otolaryngol 125
  
  Pages: 1189-1194
- Data Source
  KAKENHI-PROJECT-16659462
[Journal Article] A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss.2005
- Author(s)
  Noguchi Y, Yashima T, Hatanaka A, Uzawa M, Yasunami M, Kimura A, Kitamura K
- Journal Title
  
  Acta Otolaryngol 125
  
  Pages: 1189-1194
- Data Source
  KAKENHI-PROJECT-17390457
[Journal Article] 「ヒトの非症候群性遺伝性難聴」Hereditary Nonsyndromic Hearing Impairment2005
- Author(s)
  八島隆敏, 野口佳裕
- Journal Title
  
  細胞 The CELL 37/13
  
  Pages: 11-14
- Data Source
  KAKENHI-PROJECT-16790991
[Journal Article] SIX1 mutation associated with enlargement of the vestibular aqueduct in a patient with Branchio-Oto syndrome2005
- Author(s)
  Ito T, Noguchi Y, Yashima T, Kitamura K
- Journal Title
  
  Laryngoscope
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17390457
[Journal Article] Audiovestibular findings in patients with mitochondrial A1555G mutation.2004
- Author(s)
  Noguchi Y, Yashima T, Ito T, Sumi T, Tsuzuku T, Kitamura K
- Journal Title
  
  Laryngoscope 114
  
  Pages: 344-348
- Data Source
  KAKENHI-PROJECT-16659462
[Journal Article] Audiovestibular findings in patients with mitochondrial A1555G mutation.2004
- Author(s)
  Noguchi Y, Yashima T, Ito T, Sumi T, Tsuzuku T, Kitamura K
- Journal Title
  
  Laryngoscope 114
  
  Pages: 344-348
- Data Source
  KAKENHI-PROJECT-14370539
[Journal Article] Audiovestibular findings in patients with mitochondrial A1555G mutation.2004
- Author(s)
  Noguchi Y, Yashima T, Ito T, Sumi T, Tsuzuku T, Kitamura K
- Journal Title
  
  Laryngoscope 114
  
  Pages: 344-348
- Data Source
  KAKENHI-PROJECT-16012215
[Journal Article] A Mutation of the EYA1 gene in patients with Branchio-oto syndrome.2003
- Author(s)
  Yashima T, Noguchi Y, Ishikawa K, et al.
- Journal Title
  
  Acta Otolaryngologica 123
  
  Pages: 279-282
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14370539
[Journal Article] A Mutation of the EYA1 gene in patients with Branchio-oto syndrome.2003
- Author(s)
  Yashima T
- Journal Title
  
  Acta Otolaryngologica 123
  
  Pages: 279-282
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-14370539
[Journal Article] SIX1 mutation associated with enlargement of the vestibular aqueduct in a patient with Branchio-Oto syndrome.
- Author(s)
  Ito T, Noguchi Y, Yashima T, Kitamura K
- Journal Title
  
  Laryngoscope (in press)
- Data Source
  KAKENHI-PROJECT-17390457
[Journal Article] SIX1 mutation associated with enlargement of the vestibular aqueduct in a patient with Branchio-Oto syndrome.
- Author(s)
  Ito T, Noguchi Y, Yashima T, Kitamura K
- Journal Title
  
  Laryngoscope (in press)
- Data Source
  KAKENHI-PROJECT-16659462

1. KITAMURA Ken (90010470)

# of Collaborated Projects: 4 results

# of Collaborated Products: 9 results
2. TUNODA Atunobu (00280983)

# of Collaborated Projects: 3 results

# of Collaborated Products: 0 results
3. SUMI Takuro (20361701)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
4. KOUDA Hiroko (80334423)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
5. SUGIMOTO Taro (60262177)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
6. ITO Taku (40401400)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
7. KIKKAWA Yoshiaki (20280787)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
8. TOKANO Hisashi (70334422)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. ARIIZUMI Yosuke (30444110)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. 堤剛 (90302851)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
11. 鵜澤正道 (10361700)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. 岡村洋沖 (50244372)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. 野口佳裕 (50282752)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results

YASHIMA Takatoshi 八島 隆敏

八島 隆俊 ヤシマ タカトシ

Research Projects

Research Products

Co-Researchers

CDH23 mutation in deaf patients and experimental animals

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

難聴遺伝子解析による内耳聴覚・前庭の分子機構

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

ヒト側頭骨病理標本からレーザーキャプチャー・ダイセクションによる難聴遺伝子の抽出

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

皿型感音難聴を呈する非症候群性遺伝性難聴における難聴遺伝子の同定Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Analysis of deafness using homeobox and molecular motor gene, and knockout mouse

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss2005

Author(s)

Journal Title

Data Source

[Journal Article] A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss.2005

Author(s)

Journal Title

Data Source

[Journal Article] A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss.2005

Author(s)

Journal Title

Data Source

[Journal Article] 「ヒトの非症候群性遺伝性難聴」Hereditary Nonsyndromic Hearing Impairment2005

Author(s)

Journal Title

Data Source

[Journal Article] SIX1 mutation associated with enlargement of the vestibular aqueduct in a patient with Branchio-Oto syndrome2005

Author(s)

Journal Title

Data Source

[Journal Article] Audiovestibular findings in patients with mitochondrial A1555G mutation.2004

Author(s)

Journal Title

Data Source

[Journal Article] Audiovestibular findings in patients with mitochondrial A1555G mutation.2004

Author(s)

Journal Title

Data Source

[Journal Article] Audiovestibular findings in patients with mitochondrial A1555G mutation.2004

Author(s)

Journal Title

Data Source

[Journal Article] A Mutation of the EYA1 gene in patients with Branchio-oto syndrome.2003

Author(s)

Journal Title

Description

Data Source

[Journal Article] A Mutation of the EYA1 gene in patients with Branchio-oto syndrome.2003

Author(s)

Journal Title

Description

Data Source

[Journal Article] SIX1 mutation associated with enlargement of the vestibular aqueduct in a patient with Branchio-Oto syndrome.

Author(s)

Journal Title

YASHIMA Takatoshi 八島隆敏

八島隆俊ヤシマタカトシ