Username


Password
Forgot Password?

Preview

Isamu Yuge

Research Profile

Chemicals & Drugs

Disorders

Physiology

Procedures

Concepts & Ideas

Geographic Areas

Anatomy

Phenomena

Occupations

Register to see full profile

Co-author Network

Register to see all co-authors

Publications

  • TOP 3
  • Isamu Yuge; Yutaka Takumi; Kuni Koyabu; Shigenari Hashimoto; Seiji Takashima; Tetsuhiro Fukuyama; Toshio Nikaido; Shin-ichi Usami
    Transplanted human amniotic epithelial cells express connexin 26 and Na-K-adenosine triphosphatase in the inner ear.
  • Shin-ichi Usami; Kentaro Takahashi; Isamu Yuge; Akihiro Ohtsuka; Atsushi Namba; Satoko Abe; Erik Fransen; Laszlo Patthy; Gottfried Otting; Guy Van Camp
    Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease.
  • Akihiro Ohtsuka; Isamu Yuge; Shinobu Kimura; Atsushi Namba; Satoko Abe; Lut Van Laer; Guy Van Camp; Shin-ichi Usami
    GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation.
Register to see all publications

Register for free to view:

Visualized networks:
See your personal network in
sophisticated graphical views
GeoTargeted Searches:
Locate experts around the world
and connect with global collaborators
Research Profiles:
See the research activity
of experts around the globe
Register to see more

Geonetwork of Isamu Yuge (preview)

  • Cities where this author has publications
  • Cities where co-authors of this author have publications

Flash Player Required

Register to see more

All Publications

  • 2004: Isamu Yuge; Yutaka Takumi; Kuni Koyabu; Shigenari Hashimoto; Seiji Takashima; Tetsuhiro Fukuyama; Toshio Nikaido; Shin-ichi Usami
    Transplanted human amniotic epithelial cells express connexin 26 and Na-K-adenosine triphosphatase in the inner ear.
    Transplantation 2004;77(9):1452-4.
  • 2003: Shin-ichi Usami; Kentaro Takahashi; Isamu Yuge; Akihiro Ohtsuka; Atsushi Namba; Satoko Abe; Erik Fransen; Laszlo Patthy; Gottfried Otting; Guy Van Camp
    Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease.
    European journal of human genetics : EJHG 2003;11(10):744-8.
  • 2003: Akihiro Ohtsuka; Isamu Yuge; Shinobu Kimura; Atsushi Namba; Satoko Abe; Lut Van Laer; Guy Van Camp; Shin-ichi Usami
    GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation.
    Human genetics 2003;112(4):329-33.
  • 2002: Isamu Yuge; Akihiro Ohtsuka; Tatsuo Matsunaga; Shin-ichi Usami
    Identification of 605ins46, a novel GJB2 mutation in a Japanese family.
    Auris, nasus, larynx 2002;29(4):379-82.
  • 2002: Shin-ichi Usami; Eiko Koda; Koji Tsukamoto; Akihiro Otsuka; Isamu Yuge; Kenji Asamura; Satoko Abe; Jiro Akita; Atsushi Namba
    Molecular diagnosis of deafness: impact of gene identification.
    Audiology & neuro-otology 2002;7(3):185-90.
Register to see more
Copyright © 2011 Elsevier Inc. All rights reserved.