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Pubmed for Handhelds

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Journal Abstract Search

127 related items for PubMed ID: 31016883

  • 1. Identification of a complex genomic rearrangement in TMPRSS3 by massively parallel sequencing in Chinese cases with prelingual hearing loss.
    Li X, Tan B, Wang X, Xu X, Wang C, Zhong M, Zhao Q, Bao Z, Peng W, Zhang L, Cheng J, Lu Y, Wu P, Yuan H.
    Mol Genet Genomic Med; 2019 Jun; 7(6):e685. PubMed ID: 31016883
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  • 2. Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population.
    Gao X, Huang SS, Yuan YY, Xu JC, Gu P, Bai D, Kang DY, Han MY, Wang GJ, Zhang MG, Li J, Dai P.
    Neural Plast; 2017 Jun; 2017():3192090. PubMed ID: 28695016
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  • 3. A novel mutation of TMPRSS3 related to milder auditory phenotype in Korean postlingual deafness: a possible future implication for a personalized auditory rehabilitation.
    Chung J, Park SM, Chang SO, Chung T, Lee KY, Kim AR, Park JH, Kim V, Park WY, Oh SH, Kim D, Park WJ, Choi BY.
    J Mol Med (Berl); 2014 Jun; 92(6):651-63. PubMed ID: 24526180
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  • 8. 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; 124 Suppl 1():193S-204S. PubMed ID: 25770132
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  • 10. 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; 18(2):101-8. PubMed ID: 11462234
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  • 16. The Analysis of A Frequent TMPRSS3 Allele Containing P.V116M and P.V291L in A Cis Configuration among Deaf Koreans.
    Kim AR, Chung J, Kim NKD, Lee C, Park WY, Oh DY, Choi BY.
    Int J Mol Sci; 2017 Oct 26; 18(11):. PubMed ID: 29072634
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  • 18. The natural history and genotype-phenotype correlations of TMPRSS3 hearing loss: an international, multi-center, cohort analysis.
    Colbert BM, Lanting C, Smeal M, Blanton S, Dykxhoorn DM, Tang PC, Getchell RL, Velde H, Fehrmann M, Thorpe R, Chapagain P, Elkhaligy H, Kremer H, Yntema H, Haer-Wigman L, Redfield S, Sun T, Bruijn S, Plomp A, Goderie T, van de Kamp J, Free RH, Wassink-Ruiter JK, Widdershoven J, Vanhoutte E, Rotteveel L, Kriek M, van Dooren M, Hoefsloot L, de Gier HHW, DOOFNL Consortium, Schaefer A, Kolbe D, Azaiez H, Rabie G, Aburayyan A, Kawas M, Kanaan M, Holder J, Usami SI, Chen Z, Dai P, Holt J, Nelson R, Choi BY, Shearer E, Smith RJH, Pennings R, Liu XZ.
    Hum Genet; 2024 May 26; 143(5):721-734. PubMed ID: 38691166
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  • 20. Overinterpretation of high throughput sequencing data in medical genetics: first evidence against TMPRSS3/GJB2 digenic inheritance of hearing loss.
    Ołdak M, Lechowicz U, Pollak A, Oziębło D, Skarżyński H.
    J Transl Med; 2019 Aug 14; 17(1):269. PubMed ID: 31412945
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