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    Results: 1 to 20 of 225

    1.

    Connexins, hearing and deafness: clinical aspects of mutations in the connexin 26 gene.

    Lefebvre PP, Van De Water TR.

    Brain Res Brain Res Rev. 2000 Apr;32(1):159-62. Review.PMID: 10928803 [PubMed - indexed for MEDLINE]Related articles

    2.

    Gap junctions and connexins in the inner ear: their roles in homeostasis and deafness.

    Nickel R, Forge A.

    Curr Opin Otolaryngol Head Neck Surg. 2008 Oct;16(5):452-7. Review.PMID: 18797288 [PubMed - indexed for MEDLINE]Related articles

    3.

    [Pseudodominants of two recessive connexin mutations in non-syndromic sensorineural hearing loss?]

    Birkenhäger R, Zimmer AJ, Maier W, Schipper J.

    Laryngorhinootologie. 2006 Mar;85(3):191-6. German. PMID: 16547895 [PubMed - indexed for MEDLINE]Related articles

    4.

    Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins.

    Rabionet R, Gasparini P, Estivill X.

    Hum Mutat. 2000 Sep;16(3):190-202. Review.PMID: 10980526 [PubMed - indexed for MEDLINE]Related articles

    5.

    Potassium ion recycling pathway via gap junction systems in the mammalian cochlea and its interruption in hereditary nonsyndromic deafness.

    Kikuchi T, Adams JC, Miyabe Y, So E, Kobayashi T.

    Med Electron Microsc. 2000;33(2):51-6. Review.PMID: 11810458 [PubMed - indexed for MEDLINE]Related articles

    6.

    Connexins in hearing loss: a comprehensive overview.

    Sabag AD, Dagan O, Avraham KB.

    J Basic Clin Physiol Pharmacol. 2005;16(2-3):101-16. Review.PMID: 16285463 [PubMed - indexed for MEDLINE]Related articles

    7.

    Gap-junction channels dysfunction in deafness and hearing loss.

    Martínez AD, Acuña R, Figueroa V, Maripillan J, Nicholson B.

    Antioxid Redox Signal. 2009 Feb;11(2):309-22. Review.PMID: 18837651 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Connexin 26: required for normal auditory function.

    Kelley PM, Cohn E, Kimberling WJ.

    Brain Res Brain Res Rev. 2000 Apr;32(1):184-8. Review.PMID: 10751669 [PubMed - indexed for MEDLINE]Related articles

    9.

    Gap junctions and cochlear homeostasis.

    Zhao HB, Kikuchi T, Ngezahayo A, White TW.

    J Membr Biol. 2006 Feb-Mar;209(2-3):177-86. Epub 2006 May 17. Review.PMID: 16773501 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss.

    Cohn ES, Kelley PM.

    Am J Med Genet. 1999 Sep 24;89(3):130-6. Review.PMID: 10704187 [PubMed - indexed for MEDLINE]Related articles

    11.

    Temporal bone histopathology in connexin 26-related hearing loss.

    Jun AI, McGuirt WT, Hinojosa R, Green GE, Fischel-Ghodsian N, Smith RJ.

    Laryngoscope. 2000 Feb;110(2 Pt 1):269-75.PMID: 10680928 [PubMed - indexed for MEDLINE]Related articles

    12.

    Connexin mutations in hearing loss, dermatological and neurological disorders.

    Rabionet R, López-Bigas N, Arbonès ML, Estivill X.

    Trends Mol Med. 2002 May;8(5):205-12. Review.PMID: 12067629 [PubMed - indexed for MEDLINE]Related articles

    13.

    Gap junctions and connexin expression in the inner ear.

    Forge A, Becker D, Casalotti S, Edwards J, Evans WH, Lench N, Souter M.

    Novartis Found Symp. 1999;219:134-50; discussion 151-6. Review.PMID: 10207902 [PubMed - indexed for MEDLINE]Related articles

    14.

    Mutations in the gene for connexin 26 (GJB2) that cause hearing loss have a dominant negative effect on connexin 30.

    Marziano NK, Casalotti SO, Portelli AE, Becker DL, Forge A.

    Hum Mol Genet. 2003 Apr 15;12(8):805-12.PMID: 12668604 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment.

    Xia JH, Liu CY, Tang BS, Pan Q, Huang L, Dai HP, Zhang BR, Xie W, Hu DX, Zheng D, Shi XL, Wang DA, Xia K, Yu KP, Liao XD, Feng Y, Yang YF, Xiao JY, Xie DH, Huang JZ.

    Nat Genet. 1998 Dec;20(4):370-3. Erratum in: Nat Genet 1999 Feb;21(2):241. PMID: 9843210 [PubMed - indexed for MEDLINE]Related articles

    16.

    [From gene to disease: deafness and connexin 26]

    Hoefsloot LH, Kemperman M, Cremers CW.

    Ned Tijdschr Geneeskd. 2002 Feb 9;146(6):259-61. Dutch. PMID: 11865655 [PubMed - indexed for MEDLINE]Related articles

    17.

    Mechanism of the defect in gap-junctional communication by expression of a connexin 26 mutant associated with dominant deafness.

    Chen Y, Deng Y, Bao X, Reuss L, Altenberg GA.

    FASEB J. 2005 Sep;19(11):1516-8. Epub 2005 Jul 11.PMID: 16009703 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.

    Denoyelle F, Marlin S, Weil D, Moatti L, Chauvin P, Garabédian EN, Petit C.

    Lancet. 1999 Apr 17;353(9161):1298-303.PMID: 10218527 [PubMed - indexed for MEDLINE]Related articles

    19.

    Closing the gap on autosomal dominant connexin-26 and connexin-43 mutants linked to human disease.

    Laird DW.

    J Biol Chem. 2008 Feb 8;283(6):2997-3001. Epub 2007 Dec 18. Review.PMID: 18089569 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Connexin 26 mutations in nonsyndromic autosomal recessive hearing loss: speech and hearing rehabilitation.

    Mesolella M, Tranchino G, Nardone M, Motta S, Galli V.

    Int J Pediatr Otorhinolaryngol. 2004 Aug;68(8):995-1005.PMID: 15236885 [PubMed - indexed for MEDLINE]Related articles

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