BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 23235333)

  • 1. Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population.
    Bashir ZE; Latief N; Belyantseva IA; Iqbal F; Riazuddin SA; Khan SN; Friedman TB; Riazuddin S; Riazuddin S
    J Hum Genet; 2013 Feb; 58(2):102-8. PubMed ID: 23235333
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing loss.
    Lee K; Ansar M; Andrade PB; Khan B; Santos-Cortez RL; Ahmad W; Leal SM
    Am J Med Genet A; 2012 Feb; 158A(2):315-21. PubMed ID: 22246673
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect.
    Pater JA; Benteau T; Griffin A; Penney C; Stanton SG; Predham S; Kielley B; Squires J; Zhou J; Li Q; Abdelfatah N; O'Rielly DD; Young TL
    Hum Genet; 2017 Jan; 136(1):107-118. PubMed ID: 27838790
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in CLDN14 are associated with different hearing thresholds.
    Bashir R; Fatima A; Naz S
    J Hum Genet; 2010 Nov; 55(11):767-70. PubMed ID: 20811388
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant.
    Kitano T; Kitajiri SI; Nishio SY; Usami SI
    Int J Mol Sci; 2019 Sep; 20(18):. PubMed ID: 31527509
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss.
    Charif M; Bakhchane A; Abidi O; Boulouiz R; Eloualid A; Roky R; Rouba H; Kandil M; Lenaers G; Barakat A
    Gene; 2013 Jul; 523(1):103-5. PubMed ID: 23590985
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Different mechanisms preclude mutant CLDN14 proteins from forming tight junctions in vitro.
    Wattenhofer M; Reymond A; Falciola V; Charollais A; Caille D; Borel C; Lyle R; Estivill X; Petersen MB; Meda P; Antonarakis SE
    Hum Mutat; 2005 Jun; 25(6):543-9. PubMed ID: 15880785
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic analysis of genes related to tight junction function in the Korean population with non-syndromic hearing loss.
    Kim MA; Kim YR; Sagong B; Cho HJ; Bae JW; Kim J; Lee J; Park HJ; Choi JY; Lee KY; Kim UK
    PLoS One; 2014; 9(4):e95646. PubMed ID: 24752540
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.
    Wilcox ER; Burton QL; Naz S; Riazuddin S; Smith TN; Ploplis B; Belyantseva I; Ben-Yosef T; Liburd NA; Morell RJ; Kachar B; Wu DK; Griffith AJ; Riazuddin S; Friedman TB
    Cell; 2001 Jan; 104(1):165-72. PubMed ID: 11163249
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in
    Pandey N; Rashid T; Jalvi R; Sharma M; Rangasayee R; Andrabi KI; Anand A
    Indian J Med Res; 2017 Oct; 146(4):489-497. PubMed ID: 29434063
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Loss of inner hair cell ribbon synapses and auditory nerve fiber regression in Cldn14 knockout mice.
    Claußen M; Schulze J; Nothwang HG
    Hear Res; 2020 Jun; 391():107950. PubMed ID: 32251970
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss.
    Charif M; Boulouiz R; Bakhechane A; Benrahma H; Nahili H; Eloualid A; Rouba H; Kandil M; Abidi O; Lenaers G; Barakat A
    Indian J Hum Genet; 2013 Jul; 19(3):331-6. PubMed ID: 24339547
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic analysis of CLDN14 in the Chinese population affected with non-syndromic hearing loss.
    Lu Y; Yao J; Wei Q; Xu J; Xing G; Cao X
    Int J Pediatr Otorhinolaryngol; 2018 Feb; 105():6-11. PubMed ID: 29447821
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Segregation of p.Arg68Ter-
    Tlili A; Mutery AA; Chouchen J
    Genes (Basel); 2024 May; 15(5):. PubMed ID: 38790217
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of Hearing Loss-Associated Variants of
    Mahmood U; Bukhari SA; Ali M; Ahmed ZM; Riazuddin S
    Biomed Res Int; 2021; 2021():5584788. PubMed ID: 33997018
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration.
    Ben-Yosef T; Belyantseva IA; Saunders TL; Hughes ED; Kawamoto K; Van Itallie CM; Beyer LA; Halsey K; Gardner DJ; Wilcox ER; Rasmussen J; Anderson JM; Dolan DF; Forge A; Raphael Y; Camper SA; Friedman TB
    Hum Mol Genet; 2003 Aug; 12(16):2049-61. PubMed ID: 12913076
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Frequencies of gap- and tight-junction mutations in Turkish families with autosomal-recessive non-syndromic hearing loss.
    Uyguner O; Emiroglu M; Uzumcu A; Hafiz G; Ghanbari A; Baserer N; Yuksel-Apak M; Wollnik B
    Clin Genet; 2003 Jul; 64(1):65-9. PubMed ID: 12791041
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome.
    Ahmed ZM; Riazuddin S; Aye S; Ali RA; Venselaar H; Anwar S; Belyantseva PP; Qasim M; Riazuddin S; Friedman TB
    Hum Genet; 2008 Oct; 124(3):215-23. PubMed ID: 18719945
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome.
    Riazuddin S; Ahmed ZM; Hegde RS; Khan SN; Nasir I; Shaukat U; Riazuddin S; Butman JA; Griffith AJ; Friedman TB; Choi BY
    BMC Med Genet; 2011 Feb; 12():21. PubMed ID: 21306635
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing loss.
    Shahzad M; Sivakumaran TA; Qaiser TA; Schultz JM; Hussain Z; Flanagan M; Bhinder MA; Kissell D; Greinwald JH; Khan SN; Friedman TB; Zhang K; Riazuddin S; Riazuddin S; Ahmed ZM
    Otolaryngol Head Neck Surg; 2013 Sep; 149(3):478-87. PubMed ID: 23770805
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.