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Journal Abstract Search

174 related items for PubMed ID: 29072634

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  • 7. Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss.
    Charif M, Abidi O, Boulouiz R, Nahili H, Rouba H, Kandil M, Delprat B, Lenaers G, Barakat A.
    Biochem Biophys Res Commun; 2012 Mar 23; 419(4):643-7. PubMed ID: 22382023
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  • 11. A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein.
    Wattenhofer M, Sahin-Calapoglu N, Andreasen D, Kalay E, Caylan R, Braillard B, Fowler-Jaeger N, Reymond A, Rossier BC, Karaguzel A, Antonarakis SE.
    Hum Genet; 2005 Oct 23; 117(6):528-35. PubMed ID: 16021470
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  • 12. Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness.
    Masmoudi S, Antonarakis SE, Schwede T, Ghorbel AM, Gratri M, Pappasavas MP, Drira M, Elgaied-Boulila A, Wattenhofer M, Rossier C, Scott HS, Ayadi H, Guipponi M.
    Hum Mutat; 2001 Aug 23; 18(2):101-8. PubMed ID: 11462234
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  • 16. TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafness.
    Guipponi M, Antonarakis SE, Scott HS.
    Front Biosci; 2008 Jan 01; 13():1557-67. PubMed ID: 17981648
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  • 18. The patients associated with TMPRSS3 mutations are good candidates for electric acoustic stimulation.
    Miyagawa M, Nishio SY, Sakurai Y, Hattori M, Tsukada K, Moteki H, Kojima H, Usami S.
    Ann Otol Rhinol Laryngol; 2015 May 01; 124 Suppl 1():193S-204S. PubMed ID: 25770132
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  • 19. 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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  • 20. [Mutational analysis and prenatal diagnosis of TMPRSS3 gene in two Chinese families affected with deafness].
    Ren SM, Wu QH, Chen C, Kong XD.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2020 Apr 07; 55(4):344-349. PubMed ID: 32306631
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