Free Access
Issue
Med Sci (Paris)
Volume 21, Number 6-7, Juin–Juillet 2005
Page(s) 585 - 588
Section Nouvelles
DOI https://doi.org/10.1051/medsci/2005216-7585
Published online 15 June 2005
  1. Gerido DA, White TW. Connexin disorders of the ear, skin, and lens. Biochim Biophys Acta 2004; 1662 : 159–70. [Google Scholar]
  2. Bruzzone R, White TW, Paul, DL. Connections with connexins : the molecular basis of direct intercellular signaling. Eur J Biochem 1996; 238 : 1–27. [Google Scholar]
  3. Harris AL. Emerging issues of connexin channels : biophysics fills the gap. Q Rev Biophys 2001; 34 : 325–472. [Google Scholar]
  4. Beltramello M, Piazza V, Bukauskas FF, et al. Impaired permeability to Ins(1,4,5)P3 in a mutant connexin underlies recessive hereditary deafness. Nat Cell Biol 2005; 7 : 63–9. [Google Scholar]
  5. Petit C, Levilliers J, Hardelin JP. Molecular genetics of hearing loss. Annu Rev Genet 2001; 35 : 589–646. [Google Scholar]
  6. Lautermann J, Ten Cate WJ, Altenhoff P, et al. Expression of the gap-junction connexins 26 and 30 in the rat cochlea. Cell Tissue Res 1998; 294 : 415–20. [Google Scholar]
  7. Boettger T, Hubner CA, Maier H, et al. Deafness and renal tubular acidosis in mice lacking the K-Cl co-transporter Kcc4. Nature 2002; 416 : 874–8. [Google Scholar]
  8. Cohen-Salmon M, Ott T, Michel V, et al. Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death. Curr Biol 2002; 12 : 1106–11. [Google Scholar]
  9. Valiunas V, Manthey D, Vogel R, et al. Biophysical properties of mouse connexin30 gap junction channels studied in transfected human HeLa cells. J Physiol 1999; 519 : 631–44. [Google Scholar]
  10. Bevans CG, Kordel M, Rhee SK, Harris AL. Isoform composition of connexin channels determines selectivity among second messengers and uncharged molecules. J Biol Chem 1998; 273 : 2808–16. [Google Scholar]
  11. Goldberg GS, Lampe PD, Nicholson BJ. Selective transfer of endogenous metabolites through gap junctions composed of different connexins. Nat Cell Biol 1999; 1 : 457–9. [Google Scholar]
  12. Niessen H, Harz H, Bedner P, et al. Selective permeability of different connexin channels to the second messenger inositol 1,4,5-trisphosphate. J Cell Sci 2000; 113 : 1365–72. [Google Scholar]
  13. Bruzzone R, Gomès D, Veronesi V, et al. Functional analysis of recessive mutations of human connexin26 associated with nonsyndromic deafness. FEBS Lett 2003; 533 : 79–88. [Google Scholar]
  14. Gale JE, Piazza V, Ciubotaru CD, Mammano F. A mechanism for sensing noise damage in the inner ear. Curr Biol 2004; 14 : 526–9. [Google Scholar]
  15. Oh S, Ri Y, Bennett MV, et al. Changes in permeability caused by connexin 32 mutations underlie X-linked Charcot-Marie-Tooth disease. Neuron 1997; 19 : 927–38. [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.