REFERENCES
- Bitner-Glindzicz M (2002). Hereditary deafness and phenotyp- ing in humans. Br Med Bull 63: 73—94.
- Cohen-Salmon M, Ott T, Michel V, Hardelin JP, Perfettini I, Eybalin M, Wu T, Marcus DC, Wangemann P, Willecke K, Petit C (2002). Targeted ablation of connexin26 in the inner ear ep- ithelial gap junction network causes hearing impairment and cell death. Curr Biol 12: 1106—1111.
- Forge A, Becker D, Casalotti S, Edwards J, Marziano N, Nevill G (2003). Gap junctions in the inner ear: Comparison of distribu- tion patterns in different vertebrates and assessment of connexin composition in mammals. J Comp Neurol (in press).
- Grifa A, Wagner CA, D’Ambrosio L, Melchionda S, Bernardi F, Lopez-Bigas N, Rabionet R, Arbones M, Monica MD, Estivill X, Zelante L, Lang F, Gasparini P (1999). Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus. Nat Genet 23: 16—18.
- Jagger DJ, Robertson D, Housley GD (2000). A technique for slicing the rat cochlea around the onset of hearing. J Neurosci Meth 104: 77—86.
- Janecke AR, Nekahm D, Loffler J, Hirst-Stadlmann A, Muller T, Utermann G (2001). De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing loss. Hum. Genet 108: 269—270.
- Kudo T, Kure S, Ikeda K, Xia AP, Katori Y, Suzuki M, Kojima K, Ichinohe A, Suzuki Y, Aoki Y, Kobayashi T, Matsubara Y (2003). Transgenic expression of a dominant- negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness. Hum Mol Genet 12: 995—1004.
- Lautermann J, ten Cate WJ, Altenhoff P, Grummer R, Traub O, Frank H, Jahnke K, Winterhager E (1998). Expression of the gap-junction connexins 26 and 30 in the rat cochlea. Cell Tissue Res 294: 415—420.
- Manthey D, Banach K, Desplantez T, Lee CG, Kozak CA, Traub O, Weingart R, Willecke K (2001). Intracellular domains of mouse connexin26 and -30 affect diffusional and electrical properties of gap junction channels. J Memb Biol 181: 137—148.
- Marziano NK, Casalotti SO, Portelli AE, Becker DL, Forge A (2003). Mutations in the gene for connexin 26 (GJB2) that cause hearing loss have a dominant negative effect on connexin 30. Hum Mol Genet 12: 805—812.
- Stauffer KA, Kumar NM, Gilula NB, Unwin N (1991). Isolation and purification of gap junction channels. J Cell Biol 115: 141—150.
- Teubner B, Michel V, Pesch J, Lautermann J, Cohen-Salmon M, Sohl G, Jahnke K, Winterhager E, Herberhold C, Hardelin JP, Petit C, Willecke K (2003). Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear po- tential. Hum Mol Genet 12: 13—21.