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Expertise in Hearing Disorders: HELP
Kiyoto Kurima
Based on 8 articles published since 2009
(Why 8 articles?)
||||
Expertise Level
The expertise of Kiyoto Kurima ranks in the
  • Top 2.3%
  • ... of 62,471 published authors worldwide on Hearing Disorders
  • ... from 2009 through 2019
  • ... based on contributions to 8 articles on the topic.
Graphical view (beta)
Work Locations
Details
Most likely:    National Institutes of Health      
2017
  • Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892. · Inflammatory Disease Section, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892. · Rheumatology Fellowship and Training Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892. · Rady Children's Hospital and Department of Pediatrics, University of California, San Diego, La Jolla, CA 92093. · Office of the Clinical Director, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892. · Radiology and Imaging Sciences, Clinical Center, National Institutes of Health, Bethesda, MD 20892. · Inflammatory Disease Section, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892; · Translational Autoinflammatory Disease Studies, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892. · Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892; · Pubmed 28847925
2014
  • Molecular Biology and Genetics Section, National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, 35A Convent Dr, Bethesda, MD 20892, USA. · Department of Otolaryngology, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8519, Japan. · Molecular Biology and Genetics Section, National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, 35A Convent Dr, Bethesda, MD 20892, USA. Electronic address: · Pubmed 24933710
  • Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892, USA. · Anatomy and Physiology Department, Kansas State University, Manhattan, KS 66506, USA. · Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892, USA. · Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: · Pubmed 24561068
2014
  • National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, 20892, USA, · Pubmed 24839095
2011
  • Molecular Biology and Genetics Section, National Institute on Deafness and Other Communication Disorders, NIH, Rockville, Maryland 20850-3320, USA. · Pubmed 22105175
  • Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, NIH, Rockville, Maryland, USA. · Pubmed 21965328
Possible:    University of Maryland Baltimore   Contact    
2011
  • Department of Otorhinolaryngology-Head and Neck Surgery, University of Maryland, Baltimore, Maryland, United States of America. · Pubmed 21980309
Possible:    Universiteit Antwerpen      
2009
  • Department of Medical Genetics, University of Antwerp (UA), Antwerp, Belgium. · Pubmed 19180119
Specific Interests

In the titles of their published articles, experts often reveal their very specific interests.

Here are the titles of all articles written by Kiyoto Kurima in 2009-2019 about Hearing Disorders:

  • (no title) 2017
  • Mutations of TMC1 cause deafness by disrupting mechanoelectrical transduction. 2014
  • Hearing loss is an early consequence of Npc1 gene deletion in the mouse model of Niemann-Pick disease, type C. 2014
  • Slc26a4-insufficiency causes fluctuating hearing loss and stria vascularis dysfunction. 2014
  • Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes. 2011
  • Cell type-specific transcriptome analysis reveals a major role for Zeb1 and miR-200b in mouse inner ear morphogenesis. 2011
  • Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition. 2011
  • Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairment. 2009
Show List of Full Article Records
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National Institutes of Health
University of Maryland Baltimore
Universiteit Antwerpen
Affiliation Timeline
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National Institutes of Health
2017
  • Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892. · Inflammatory Disease Section, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892. · Rheumatology Fellowship and Training Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892. · Rady Children's Hospital and Department of Pediatrics, University of California, San Diego, La Jolla, CA 92093. · Office of the Clinical Director, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892. · Radiology and Imaging Sciences, Clinical Center, National Institutes of Health, Bethesda, MD 20892. · Inflammatory Disease Section, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892; · Translational Autoinflammatory Disease Studies, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892. · Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892; · Pubmed 28847925
2014
  • Molecular Biology and Genetics Section, National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, 35A Convent Dr, Bethesda, MD 20892, USA. · Department of Otolaryngology, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8519, Japan. · Molecular Biology and Genetics Section, National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, 35A Convent Dr, Bethesda, MD 20892, USA. Electronic address: · Pubmed 24933710
  • Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892, USA. · Anatomy and Physiology Department, Kansas State University, Manhattan, KS 66506, USA. · Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892, USA. · Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892, USA. Electronic address: · Pubmed 24561068
2014
  • National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, 20892, USA, · Pubmed 24839095
2011
  • Molecular Biology and Genetics Section, National Institute on Deafness and Other Communication Disorders, NIH, Rockville, Maryland 20850-3320, USA. · Pubmed 22105175
  • Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, NIH, Rockville, Maryland, USA. · Pubmed 21965328
University of Maryland Baltimore
2011
  • Department of Otorhinolaryngology-Head and Neck Surgery, University of Maryland, Baltimore, Maryland, United States of America. · Pubmed 21980309
Universiteit Antwerpen
2009
  • Department of Medical Genetics, University of Antwerp (UA), Antwerp, Belgium. · Pubmed 19180119
Yearly article counts 00100300301
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