201 related articles for article (PubMed ID: 21786053)
1. 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]
2. 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]
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
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. 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; ; 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; 143(5):721-734. PubMed ID: 38691166
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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; 865():147335. PubMed ID: 36871673
[TBL] [Abstract][Full Text] [Related]
14. Association of Genetic Diagnoses for Childhood-Onset Hearing Loss With Cochlear Implant Outcomes.
Carlson RJ; Walsh T; Mandell JB; Aburayyan A; Lee MK; Gulsuner S; Horn DL; Ou HC; Sie KCY; Mancl L; Rubinstein J; King MC
JAMA Otolaryngol Head Neck Surg; 2023 Mar; 149(3):212-222. PubMed ID: 36633841
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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; 117(6):528-35. PubMed ID: 16021470
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Cochlear Implantation and Electric Acoustic Stimulation in Children With TMPRSS3 Genetic Mutation.
Holder JT; Morrel W; Rivas A; Labadie RF; Gifford RH
Otol Neurotol; 2021 Mar; 42(3):396-401. PubMed ID: 33555745
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]