These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 28246597)

  • 1. Novel Mutations and Mutation Combinations of
    Gao X; Yuan YY; Wang GJ; Xu JC; Su Y; Lin X; Dai P
    Biomed Res Int; 2017; 2017():4707315. PubMed ID: 28246597
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 44(6):e81. PubMed ID: 17551081
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of
    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; 2017():3192090. PubMed ID: 28695016
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genotype-Phenotype Correlations in TMPRSS3 (DFNB10/DFNB8) with Emphasis on Natural History.
    Nisenbaum E; Yan D; Shearer AE; de Joya E; Thielhelm T; Russell N; Staecker H; Chen Z; Holt JR; Liu X
    Audiol Neurootol; 2023; 28(6):407-419. PubMed ID: 37331337
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 12(6):753-66. PubMed ID: 21786053
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 532(2):276-80. PubMed ID: 23958653
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 9(12):e114136. PubMed ID: 25474651
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 18(11):. PubMed ID: 29072634
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 5():24. PubMed ID: 15447792
    [TBL] [Abstract][Full Text] [Related]  

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

  • 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; 18(2):101-8. PubMed ID: 11462234
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 419(4):643-7. PubMed ID: 22382023
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prediction of cochlear implant performance by genetic mutation: the spiral ganglion hypothesis.
    Eppsteiner RW; Shearer AE; Hildebrand MS; Deluca AP; Ji H; Dunn CC; Black-Ziegelbein EA; Casavant TL; Braun TA; Scheetz TE; Scherer SE; Hansen MR; Gantz BJ; Smith RJ
    Hear Res; 2012 Oct; 292(1-2):51-8. PubMed ID: 22975204
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 80(2):124-31. PubMed ID: 11907649
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Late-onset hereditary hearing loss caused by
    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; 38(8):679-686. PubMed ID: 39118504
    [No Abstract]   [Full Text] [Related]  

  • 18. Novel TMPRSS3 variants in Pakistani families with autosomal recessive non-syndromic hearing impairment.
    Lee K; Khan S; Islam A; Ansar M; Andrade PB; Kim S; Santos-Cortez RL; Ahmad W; Leal SM
    Clin Genet; 2012 Jul; 82(1):56-63. PubMed ID: 21534946
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 31(9):2796-2810. PubMed ID: 37244253
    [TBL] [Abstract][Full Text] [Related]  

  • 20. TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafness.
    Guipponi M; Antonarakis SE; Scott HS
    Front Biosci; 2008 Jan; 13():1557-67. PubMed ID: 17981648
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.