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Journal Abstract Search

241 related items for PubMed ID: 24933710

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  • 2. Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 function.
    Nakanishi H, Kurima K, Pan B, Wangemann P, Fitzgerald TS, Géléoc GS, Holt JR, Griffith AJ.
    Sci Rep; 2018 Aug 14; 8(1):12125. PubMed ID: 30108230
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  • 4. Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
    Kurima K, Peters LM, Yang Y, Riazuddin S, Ahmed ZM, Naz S, Arnaud D, Drury S, Mo J, Makishima T, Ghosh M, Menon PS, Deshmukh D, Oddoux C, Ostrer H, Khan S, Riazuddin S, Deininger PL, Hampton LL, Sullivan SL, Battey JF, Keats BJ, Wilcox ER, Friedman TB, Griffith AJ.
    Nat Genet; 2002 Mar 14; 30(3):277-84. PubMed ID: 11850618
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  • 5. The contribution of TMC1 to adaptation of mechanoelectrical transduction channels in cochlear outer hair cells.
    Goldring AC, Beurg M, Fettiplace R.
    J Physiol; 2019 Dec 14; 597(24):5949-5961. PubMed ID: 31633194
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  • 6. A novel DFNA36 mutation in TMC1 orthologous to the Beethoven (Bth) mouse associated with autosomal dominant hearing loss in a Chinese family.
    Zhao Y, Wang D, Zong L, Zhao F, Guan L, Zhang P, Shi W, Lan L, Wang H, Li Q, Han B, Yang L, Jin X, Wang J, Wang J, Wang Q.
    PLoS One; 2014 Dec 14; 9(5):e97064. PubMed ID: 24827932
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  • 7. [Advances in hereditary hearing loss caused by TMC1 mutations].
    Wu K, Wang H, Wang Q.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2016 Mar 14; 51(3):224-9. PubMed ID: 27033582
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  • 13. Mouse tales from Kresge: the deafness mouse.
    Drury SS, Keats BJ.
    J Am Acad Audiol; 2003 Aug 14; 14(6):296-301. PubMed ID: 14552423
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  • 14. Novel autosomal dominant TMC1 variants linked to hearing loss: insight into protein-lipid interactions.
    Cho SH, Yun Y, Lee DH, Cha JH, Lee SM, Lee J, Suh MH, Lee JH, Oh SH, Park MK, Lee SY.
    BMC Med Genomics; 2023 Dec 08; 16(1):320. PubMed ID: 38066485
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  • 15. Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes.
    Kawashima Y, Géléoc GS, Kurima K, Labay V, Lelli A, Asai Y, Makishima T, Wu DK, Della Santina CC, Holt JR, Griffith AJ.
    J Clin Invest; 2011 Dec 08; 121(12):4796-809. PubMed ID: 22105175
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  • 17. Identification of TMC1 as a relatively common cause for nonsyndromic hearing loss in the Saudi population.
    Ramzan K, Al-Owain M, Al-Numair NS, Afzal S, Al-Ageel S, Al-Amer S, Al-Baik L, Al-Otaibi GF, Hashem A, Al-Mashharawi E, Basit S, Al-Mazroea AH, Softah A, Sogaty S, Imtiaz F.
    Am J Med Genet B Neuropsychiatr Genet; 2020 Apr 08; 183(3):172-180. PubMed ID: 31854501
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  • 18. Tmc1 Point Mutation Affects Ca2+ Sensitivity and Block by Dihydrostreptomycin of the Mechanoelectrical Transducer Current of Mouse Outer Hair Cells.
    Corns LF, Johnson SL, Kros CJ, Marcotti W.
    J Neurosci; 2016 Jan 13; 36(2):336-49. PubMed ID: 26758827
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  • 19. Optimized AAV Vectors for TMC1 Gene Therapy in a Humanized Mouse Model of DFNB7/11.
    Marcovich I, Baer NK, Shubina-Oleinik O, Eclov R, Beard CW, Holt JR.
    Biomolecules; 2022 Jun 29; 12(7):. PubMed ID: 35883470
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  • 20. Novel TMC1 structural and splice variants associated with congenital nonsyndromic deafness in a Sudanese pedigree.
    Meyer CG, Gasmelseed NM, Mergani A, Magzoub MM, Muntau B, Thye T, Horstmann RD.
    Hum Mutat; 2005 Jan 29; 25(1):100. PubMed ID: 15605408
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