Journal home
Advance online publication
Current issue
Archive
Press releases
Supplements
Focuses
Guide to authors
Online submissionOnline submission
For referees
Free online issue
Contact the journal
Subscribe
Advertising
work@npg
Reprints and permissions
About this site
For librarians
 
NPG Resources
Nature
Nature Reviews
Nature Immunology
Nature Cell Biology
Nature Genetics
news@nature.com
Nature Conferences
Dissect Medicine
NPG Subject areas
Biotechnology
Cancer
Chemistry
Clinical Medicine
Dentistry
Development
Drug Discovery
Earth Sciences
Evolution & Ecology
Genetics
Immunology
Materials Science
Medical Research
Microbiology
Molecular Cell Biology
Neuroscience
Pharmacology
Physics
Browse all publications
News and Views
Nature Medicine  3, 608 - 609 (1997)
doi:10.1038/nm0697-608

Motors, channels and the sounds of silence

Karen B. Avraham

Department of Human Genetics, Tel Aviv University, Ramat Aviv, Tel Aviv 69978, Israel

Mutations in myosin VIIA and connexin 26 lead to hereditary non-syndromic hearing loss

REFERENCES
  1. Kelsell, D.P. et al. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness (DFNA3 and DFNB1). Nature 387, 80−83 (1997). | Article | PubMed  | ISI | ChemPort |
  2. Liu, X.-Z. et al. Mutations in the myosin VIIA gene cause non-syndromic recessive deafness. Nature Genet 16, 188−190 (1997). | Article | PubMed  | ISI | ChemPort |
  3. Weil, D. et al. The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin VIIA gene. Nature Genet. 16, 191−193 (1997). | Article | PubMed  | ISI | ChemPort |
  4. Waelsch, S.G. Genetics of hearing impairment. NY Acad. Sci. 630, 3−5 (1991).
  5. Morton, N.E. Genetic epidemiology of hearing impairment. Ann. NY Acad. Sci. 630, 16−31 (1991). | PubMed  | ChemPort |
  6. Gibson, F. et al. A type VII myosin encoded by the mouse deafness gene shaker-1. Nature 374, 62−64 (1995). | Article | PubMed  | ISI | ChemPort |
  7. Avraham, K.B. et al. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for the structural integrity of inner ear hair cells. Nature Genet. 11, 369−375 (1995). | Article | PubMed  | ISI | ChemPort |
  8. Weil, D. et al. Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature 374, 60−61 (1995). | Article | PubMed  | ISI | ChemPort |
  9. Hasson, T. et al. Unconventional myosins in inner ear sensory epithelia. J. Cell Biol. (1997) in press. | PubMed  |
  10. Kikuchi, T., Kimura, R.S., Paul, D.L. & Adams, J.C. Gap junctions in the rat cochlea: immuno-histochemical and ultrastructural analysis. Anat. Embryol. 191, 101−118 (1995). | ChemPort |
  11. Solomon, A. Deaf is beautiful. N.Y. Times Magazine. August 28, section 6 (1994).
 Top
 Top
References
Previous | Next
Table of contents
Download PDFDownload PDF
Send to a friendSend to a friend
Save this linkSave this link

Open Innovation Challenges

  • Optimizing Sub-cellular Localization Tags

    • Deadline: Nov 29 2009
    • Reward: $20,000 USD

    The Seeker is looking for methods to optimize sub-cellular localization tags for protein expression....

  • Single-cell Analysis Platform

    • Deadline: Dec 02 2009
    • Reward: $5,000 USD

    This Challenge is looking for novel approaches to analyzing changes at a single-cell level. This is...

naturejobs

References
Export citation
Export references
natureproducts

Search buyers guide:

 
ADVERTISEMENT
 
Nature Medicine
ISSN: 1078-8956
EISSN: 1546-170X
Journal home | Advance online publication | Current issue | Archive | Press releases | Supplements | Focuses | For authors | Online submission | For referees | Free online issue | About the journal | Contact the journal | Subscribe | Advertising | work@npg | Reprints and permissions | About this site | For librarians
Nature Publishing Group, publisher of Nature, and other science journals and reference works©1997 Nature Publishing Group | Privacy policy