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Journal Abstract Search

401 related items for PubMed ID: 11850623

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  • 3. Mutations of TMC1 cause deafness by disrupting mechanoelectrical transduction.
    Nakanishi H, Kurima K, Kawashima Y, Griffith AJ.
    Auris Nasus Larynx; 2014 Oct; 41(5):399-408. PubMed ID: 24933710
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  • 5. Identification of three novel hearing loss mouse strains with mutations in the Tmc1 gene.
    Manji SS, Miller KA, Williams LH, Dahl HH.
    Am J Pathol; 2012 Apr; 180(4):1560-9. PubMed ID: 22330676
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  • 7. Tmc1 is necessary for normal functional maturation and survival of inner and outer hair cells in the mouse cochlea.
    Marcotti W, Erven A, Johnson SL, Steel KP, Kros CJ.
    J Physiol; 2006 Aug 01; 574(Pt 3):677-98. PubMed ID: 16627570
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  • 8. Tmc gene therapy restores auditory function in deaf mice.
    Askew C, Rochat C, Pan B, Asai Y, Ahmed H, Child E, Schneider BL, Aebischer P, Holt JR.
    Sci Transl Med; 2015 Jul 08; 7(295):295ra108. PubMed ID: 26157030
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  • 9. Progressive sensorineural hearing loss and normal vestibular function in a Dutch DFNB7/11 family with a novel mutation in TMC1.
    de Heer AM, Collin RW, Huygen PL, Schraders M, Oostrik J, Rouwette M, Kunst HP, Kremer H, Cremers CW.
    Audiol Neurootol; 2011 Jul 08; 16(2):93-105. PubMed ID: 21252500
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  • 10. Mouse models to study inner ear development and hereditary hearing loss.
    Friedman LM, Dror AA, Avraham KB.
    Int J Dev Biol; 2007 Jul 08; 51(6-7):609-31. PubMed ID: 17891721
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  • 11. New Tmc1 Deafness Mutations Impact Mechanotransduction in Auditory Hair Cells.
    Beurg M, Schimmenti LA, Koleilat A, Amr SS, Oza A, Barlow AJ, Ballesteros A, Fettiplace R.
    J Neurosci; 2021 May 19; 41(20):4378-4391. PubMed ID: 33824189
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  • 12. Circling mouse: possible animal model for deafness.
    Lee JW, Lee EJ, Hong SH, Chung WH, Lee HT, Lee TW, Lee JR, Kim HT, Suh JG, Kim TY, Ryoo ZY.
    Comp Med; 2001 Dec 19; 51(6):550-4. PubMed ID: 11924819
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  • 13. Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11.
    Hilgert N, Alasti F, Dieltjens N, Pawlik B, Wollnik B, Uyguner O, Delmaghani S, Weil D, Petit C, Danis E, Yang T, Pandelia E, Petersen MB, Goossens D, Favero JD, Sanati MH, Smith RJ, Van Camp G.
    Clin Genet; 2008 Sep 19; 74(3):223-32. PubMed ID: 18616530
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  • 14. Cochlear pathology of the circling mouse: a new mouse model of DFNB6.
    Chung WH, Kim KR, Cho YS, Cho DY, Woo JH, Ryoo ZY, Cho KI, Hong SH.
    Acta Otolaryngol; 2007 Mar 19; 127(3):244-51. PubMed ID: 17364360
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  • 15. Ectopic expression of tmie transgene induces various recovery levels of behavior and hearing ability in the circling mouse.
    Shin MJ, Lee JH, Yu DH, Kim BS, Kim HJ, Kim SH, Kim MO, Park C, Hyun BH, Lee S, So HS, Park R, Ryoo ZY.
    Biochem Biophys Res Commun; 2008 Sep 12; 374(1):17-21. PubMed ID: 18586001
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  • 16. Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan.
    Kitajiri SI, McNamara R, Makishima T, Husnain T, Zafar AU, Kittles RA, Ahmed ZM, Friedman TB, Riazuddin S, Griffith AJ.
    Clin Genet; 2007 Dec 12; 72(6):546-50. PubMed ID: 17877751
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  • 17. Characterisation of DRASIC in the mouse inner ear.
    Hildebrand MS, de Silva MG, Klockars T, Rose E, Price M, Smith RJ, McGuirt WT, Christopoulos H, Petit C, Dahl HH.
    Hear Res; 2004 Apr 12; 190(1-2):149-60. PubMed ID: 15051137
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  • 18. A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1.
    Kitajiri S, Makishima T, Friedman TB, Griffith AJ.
    Clin Genet; 2007 Feb 12; 71(2):148-52. PubMed ID: 17250663
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  • 19. The circling mouse (C57BL/6J-cir) has a 40-kilobase genomic deletion that includes the transmembrane inner ear (tmie) gene.
    Cho KI, Suh JG, Lee JW, Hong SH, Kang TC, Oh YS, Ryoo ZY.
    Comp Med; 2006 Dec 12; 56(6):476-81. PubMed ID: 17219777
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  • 20. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells.
    Avraham KB, Hasson T, Steel KP, Kingsley DM, Russell LB, Mooseker MS, Copeland NG, Jenkins NA.
    Nat Genet; 1995 Dec 12; 11(4):369-75. PubMed ID: 7493015
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