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Pubmed for Handhelds

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Journal Abstract Search

159 related items for PubMed ID: 16021470

  • 21. Rescue of auditory function by a single administration of AAV-TMPRSS3 gene therapy in aged mice of human recessive deafness DFNB8.
    Du W, Ergin V, Loeb C, Huang M, Silver S, Armstrong AM, Huang Z, Gurumurthy CB, Staecker H, Liu X, Chen ZY.
    Mol Ther; 2023 Sep 06; 31(9):2796-2810. PubMed ID: 37244253
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  • 23. An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing loss.
    Guipponi M, Toh MY, Tan J, Park D, Hanson K, Ballana E, Kwong D, Cannon PZ, Wu Q, Gout A, Delorenzi M, Speed TP, Smith RJ, Dahl HH, Petersen M, Teasdale RD, Estivill X, Park WJ, Scott HS.
    Hum Mutat; 2008 Jan 06; 29(1):130-41. PubMed ID: 17918732
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  • 28. Tmprss3, a transmembrane serine protease deficient in human DFNB8/10 deafness, is critical for cochlear hair cell survival at the onset of hearing.
    Fasquelle L, Scott HS, Lenoir M, Wang J, Rebillard G, Gaboyard S, Venteo S, François F, Mausset-Bonnefont AL, Antonarakis SE, Neidhart E, Chabbert C, Puel JL, Guipponi M, Delprat B.
    J Biol Chem; 2011 May 13; 286(19):17383-97. PubMed ID: 21454591
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  • 31. Structural analysis of pathogenic TMPRSS3 variants and their cochlear implantation outcomes of sensorineural hearing loss.
    Lee SJ, Lee S, Han JH, Choi BY, Lee JH, Lee DH, Lee SY, Oh SH.
    Gene; 2023 May 20; 865():147335. PubMed ID: 36871673
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  • 32. A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12.
    Shaikh RS, Ramzan K, Nazli S, Sattar S, Khan SN, Riazuddin S, Ahmed ZM, Friedman TB, Riazuddin S.
    Am J Med Genet A; 2005 Nov 01; 138(4):392-5. PubMed ID: 16158433
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  • 35. Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness.
    Delmaghani S, Aghaie A, Michalski N, Bonnet C, Weil D, Petit C.
    Hum Mol Genet; 2012 Sep 01; 21(17):3835-44. PubMed ID: 22678063
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  • 37. Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.
    Naz S, Giguere CM, Kohrman DC, Mitchem KL, Riazuddin S, Morell RJ, Ramesh A, Srisailpathy S, Deshmukh D, Riazuddin S, Griffith AJ, Friedman TB, Smith RJ, Wilcox ER.
    Am J Hum Genet; 2002 Sep 01; 71(3):632-6. PubMed ID: 12145746
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  • 40. 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 01; 72(6):546-50. PubMed ID: 17877751
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