Free Access
Med Sci (Paris)
Volume 20, Number 3, Mars 2004
Page(s) 311 - 316
Section M/S revues
Published online 15 March 2004
  1. Dallos P, Popper AN, Fay RR. The cochlea. New York : Springer, 1996. [Google Scholar]
  2. Dulon D, Aran JM. Aspects cellulaires et moléculaires de la transduction mécano-sensorielle dans l’oreille interne. Med Sci (Paris) 1990; 6 : 744–54. [Google Scholar]
  3. Sterkers O, Ferrary E, Tran Ba Huy P. Production des liquides de l’oreille interne. Med Sci (Paris) 1990; 6 : 755–61. [Google Scholar]
  4. Von Békésy G. Experiments in hearing. New York : McGraw-Hill, 1960. [Google Scholar]
  5. Dallos P, Fakler B. Prestin, a new type of motor protein. Nat Rev Mol Cell Biol 2002; 3 : 104–11. [Google Scholar]
  6. Gorlin RJ. Hereditary hearing loss and its syndromes. New York : Oxford University Press, 1995. [Google Scholar]
  7. Petit C, Levilliers J, Marlin S, Hardelin JP. Hereditary hearing loss. In : Scriver CR, Beaudet AL, Sly WS, Valle D, eds The metabolic and molecular bases of inherited disease. New York : McGraw-Hill, 2001 : 6281–328. [Google Scholar]
  8. Petit C, Levilliers J, Hardelin JP. Molecular genetics of hearing loss. Annu Rev Genet 2001; 35 : 589–646. [Google Scholar]
  9. Friedman T, Battey J, Kachar B, et al. Modifier genes of hereditary hearing loss. Curr Opin Neurobiol 2000; 10 : 487–93. [Google Scholar]
  10. Riazuddin S, Castelein CM, Ahmed ZM, et al. Dominant modifier DFNM1 suppresses recessive deafness DFNB26. Nat Genet 2000; 26 : 431–4. [Google Scholar]
  11. Nadeau JH. Modifier genes in mice and humans. Nat Rev Genet 2001; 2 : 165–74. [Google Scholar]
  12. Haider NB, Ikeda A, Naggert JK, Nishina PM. Genetic modifiers of vision and hearing. Hum Mol Genet 2002; 11 : 1195–206. [Google Scholar]
  13. Chen W, Campbell CA, Green GE, et al. Linkage of otosclerosis to a third locus (OTSC3) on human chromosome 6p21.3-22.3. J Med Genet 2002; 39 : 473–7. [Google Scholar]
  14. Gilgenkrantz S. K+, le Seigneur des anneaux… de la cochlée. Med Sci (Paris) 2000; 16 : 270–2. [Google Scholar]
  15. Petit C. Usher syndrome : from genetics to pathogenesis. Annu Rev Genom Hum Genet 2001; 2 : 271–97. [Google Scholar]
  16. Steel KP. Inherited hearing defects in mice. Annu Rev Genet 1995; 29 : 675–701. [Google Scholar]
  17. Anagnostopoulos AV. A compendium of mouse knockouts with inner ear defects. Trends Genet 2002; 18 : S21–38. [Google Scholar]
  18. Johnson KR, Zheng Qing Y, Bykhovskaya Y, et al. A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice. Nat Genet 2001; 27 : 191–4. [Google Scholar]
  19. Ikeda A, Zheng QY, Zuberi AR, et al. Microtubule-associated protein 1A is a modifier of tubby hearing (moth1). Nat Genet 2002; 30 : 401–5. [Google Scholar]
  20. Noben-Trauth K, Zheng QY, Johnson KR. Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss. Nat Genet 2003; 35 : 21–3. [Google Scholar]

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.