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197 related items for PubMed ID: 26036852

  • 1. TMPRSS3 mutations in autosomal recessive nonsyndromic hearing loss.
    Battelino S, Klancar G, Kovac J, Battelino T, Trebusak Podkrajsek K.
    Eur Arch Otorhinolaryngol; 2016 May; 273(5):1151-4. PubMed ID: 26036852
    [Abstract] [Full Text] [Related]

  • 2. Genetic analysis of TMPRSS3 gene in the Korean population with autosomal recessive nonsyndromic hearing loss.
    Lee J, Baek JI, Choi JY, Kim UK, Lee SH, Lee KY.
    Gene; 2013 Dec 15; 532(2):276-80. PubMed ID: 23958653
    [Abstract] [Full Text] [Related]

  • 3. 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 Dec 15; 2017():3192090. PubMed ID: 28695016
    [Abstract] [Full Text] [Related]

  • 4. Autosomal recessive postlingual hearing loss (DFNB8): compound heterozygosity for two novel TMPRSS3 mutations in German siblings.
    Elbracht M, Senderek J, Eggermann T, Thürmer C, Park J, Westhofen M, Zerres K.
    J Med Genet; 2007 Jun 15; 44(6):e81. PubMed ID: 17551081
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 92(6):651-63. PubMed ID: 24526180
    [Abstract] [Full Text] [Related]

  • 6. Novel Mutations and Mutation Combinations of TMPRSS3 Cause Various Phenotypes in One Chinese Family with Autosomal Recessive Hearing Impairment.
    Gao X, Yuan YY, Wang GJ, Xu JC, Su Y, Lin X, Dai P.
    Biomed Res Int; 2017 Jun 15; 2017():4707315. PubMed ID: 28246597
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan.
    Ahmed ZM, Li XC, Powell SD, Riazuddin S, Young TL, Ramzan K, Ahmad Z, Luscombe S, Dhillon K, MacLaren L, Ploplis B, Shotland LI, Ives E, Riazuddin S, Friedman TB, Morell RJ, Wilcox ER.
    BMC Med Genet; 2004 Sep 24; 5():24. PubMed ID: 15447792
    [Abstract] [Full Text] [Related]

  • 9. Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients.
    Wattenhofer M, Di Iorio MV, Rabionet R, Dougherty L, Pampanos A, Schwede T, Montserrat-Sentis B, Arbones ML, Iliades T, Pasquadibisceglie A, D'Amelio M, Alwan S, Rossier C, Dahl HH, Petersen MB, Estivill X, Gasparini P, Scott HS, Antonarakis SE.
    J Mol Med (Berl); 2002 Feb 24; 80(2):124-31. PubMed ID: 11907649
    [Abstract] [Full Text] [Related]

  • 10. Novel Mutations in the TMPRSS3 Gene may Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss.
    Wong SH, Yen YC, Li SY, Yang JJ.
    Int J Mol Sci; 2020 Mar 30; 21(7):. PubMed ID: 32235586
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. [Late-onset hereditary hearing loss caused by TMPRSS3 compound heterozygous mutations].
    Wang Y, Liang Y, Huang B, Cen X, Huang L, Chen K.
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2024 Aug 26; 38(8):679-686. PubMed ID: 39118504
    [Abstract] [Full Text] [Related]

  • 13. Identification of a novel homozygous mutation, TMPRSS3: c.535G>A, in a Tibetan family with autosomal recessive non-syndromic hearing loss.
    Fan D, Zhu W, Li D, Ji D, Wang P.
    PLoS One; 2014 Aug 26; 9(12):e114136. PubMed ID: 25474651
    [Abstract] [Full Text] [Related]

  • 14. GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants.
    Koohiyan M, Hashemzadeh-Chaleshtori M, Salehi M, Abtahi H, Reiisi S, Pourreza MR, Noori-Daloii MR, Tabatabaiefar MA.
    Int J Pediatr Otorhinolaryngol; 2018 Apr 26; 107():121-126. PubMed ID: 29501291
    [Abstract] [Full Text] [Related]

  • 15. GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran.
    Abbaspour Rodbaneh E, Panahi M, Rahimi B, Mokabber H, Farajollahi R, Davarnia B.
    J Clin Lab Anal; 2021 Nov 26; 35(11):e24024. PubMed ID: 34581455
    [Abstract] [Full Text] [Related]

  • 16. Putative TMPRSS3/GJB2 digenic inheritance of hearing loss detected by targeted resequencing.
    Leone MP, Palumbo P, Ortore R, Castellana S, Palumbo O, Melchionda S, Palladino T, Stallone R, Mazza T, Cocchi R, Carella M.
    Mol Cell Probes; 2017 Jun 26; 33():24-27. PubMed ID: 28263784
    [Abstract] [Full Text] [Related]

  • 17. Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.
    AitRaise I, Amalou G, Bakhchane A, Bousfiha A, Abdelghaffar H, Majida C, Bonnet C, Petit C, Barakat A.
    Biochem Genet; 2024 Jun 26; 62(3):1914-1924. PubMed ID: 37777971
    [Abstract] [Full Text] [Related]

  • 18. Genotype-phenotype correlation in DFNB8/10 families with TMPRSS3 mutations.
    Weegerink NJ, Schraders M, Oostrik J, Huygen PL, Strom TM, Granneman S, Pennings RJ, Venselaar H, Hoefsloot LH, Elting M, Cremers CW, Admiraal RJ, Kremer H, Kunst HP.
    J Assoc Res Otolaryngol; 2011 Dec 26; 12(6):753-66. PubMed ID: 21786053
    [Abstract] [Full Text] [Related]

  • 19. 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 26; 124 Suppl 1():193S-204S. PubMed ID: 25770132
    [Abstract] [Full Text] [Related]

  • 20. Detection of the 35delG/GJB2 and del(GJB6-D13S1830) mutations in Venezuelan patients with autosomal recessive nonsyndromic hearing loss.
    Utrera R, Ridaura V, Rodríguez Y, Rojas MJ, Mago L, Angeli S, Henríquez O.
    Genet Test; 2007 May 26; 11(4):347-52. PubMed ID: 18294049
    [Abstract] [Full Text] [Related]

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