BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

324 related articles for article (PubMed ID: 25801282)

  • 21. A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families.
    Riahi Z; Chahed H; Jaafoura H; Zainine R; Messaoud O; Naili M; Nagara M; Hammami H; Laroussi N; Bouyacoub Y; Kefi R; Bonnet C; Besbes G; Abdelhak S
    Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1485-8. PubMed ID: 23856379
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Connexin 26 (GJB2) gene-related deafness and speech intelligibility after cochlear implantation.
    Sinnathuray AR; Toner JG; Clarke-Lyttle J; Geddis A; Patterson CC; Hughes AE
    Otol Neurotol; 2004 Nov; 25(6):935-42. PubMed ID: 15547423
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.
    Green GE; Scott DA; McDonald JM; Woodworth GG; Sheffield VC; Smith RJ
    JAMA; 1999 Jun; 281(23):2211-6. PubMed ID: 10376574
    [TBL] [Abstract][Full Text] [Related]  

  • 24. In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca
    Fukunaga I; Fujimoto A; Hatakeyama K; Aoki T; Nishikawa A; Noda T; Minowa O; Kurebayashi N; Ikeda K; Kamiya K
    Stem Cell Reports; 2016 Dec; 7(6):1023-1036. PubMed ID: 27840044
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Auditory perception and speech discrimination after cochlear implantation in patients with connexin 26 (GJB2) gene-related deafness.
    Sinnathuray AR; Toner JG; Geddis A; Clarke-Lyttle J; Patterson CC; Hughes AE
    Otol Neurotol; 2004 Nov; 25(6):930-4. PubMed ID: 15547422
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA).
    Prasad S; Cucci RA; Green GE; Smith RJ
    Hum Mutat; 2000 Dec; 16(6):502-8. PubMed ID: 11102979
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Connexin26 (GJB2) deficiency reduces active cochlear amplification leading to late-onset hearing loss.
    Zhu Y; Chen J; Liang C; Zong L; Chen J; Jones RO; Zhao HB
    Neuroscience; 2015 Jan; 284():719-729. PubMed ID: 25451287
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Gap junctions and connexins in the inner ear: their roles in homeostasis and deafness.
    Nickel R; Forge A
    Curr Opin Otolaryngol Head Neck Surg; 2008 Oct; 16(5):452-7. PubMed ID: 18797288
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss.
    Cohn ES; Kelley PM
    Am J Med Genet; 1999 Sep; 89(3):130-6. PubMed ID: 10704187
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Generation of Functional CX26-Gap-Junction-Plaque-Forming Cells with Spontaneous Ca
    Fukunaga I; Fujimoto A; Hatakeyama K; Kurebayashi N; Ikeda K; Kamiya K
    Curr Protoc Stem Cell Biol; 2019 Dec; 51(1):e100. PubMed ID: 31756039
    [TBL] [Abstract][Full Text] [Related]  

  • 31. GJB2 (Cx26) gene mutations in Chinese patients with congenital sensorineural deafness and a report of one novel mutation.
    Xiao ZA; Xie DH
    Chin Med J (Engl); 2004 Dec; 117(12):1797-801. PubMed ID: 15603707
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness.
    Kelsell DP; Dunlop J; Stevens HP; Lench NJ; Liang JN; Parry G; Mueller RF; Leigh IM
    Nature; 1997 May; 387(6628):80-3. PubMed ID: 9139825
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Non-invasive screening for GJB2 mutations in buccal smears for the diagnosis of inherited hearing impairment].
    Schade G; Kothe C; Ruge G; Hess M; Meyer CG
    Laryngorhinootologie; 2003 Jun; 82(6):397-401. PubMed ID: 12851846
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews.
    Lerer I; Sagi M; Ben-Neriah Z; Wang T; Levi H; Abeliovich D
    Hum Mutat; 2001 Nov; 18(5):460. PubMed ID: 11668644
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel dominant and a de novo mutation in the GJB2 gene (connexin-26) cause keratitis-ichthyosis-deafness syndrome: implication for cochlear implantation.
    Arndt S; Aschendorff A; Schild C; Beck R; Maier W; Laszig R; Birkenhäger R
    Otol Neurotol; 2010 Feb; 31(2):210-5. PubMed ID: 20101161
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Temporal bone histopathology in connexin 26-related hearing loss.
    Jun AI; McGuirt WT; Hinojosa R; Green GE; Fischel-Ghodsian N; Smith RJ
    Laryngoscope; 2000 Feb; 110(2 Pt 1):269-75. PubMed ID: 10680928
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Hearing is normal without connexin30.
    Boulay AC; del Castillo FJ; Giraudet F; Hamard G; Giaume C; Petit C; Avan P; Cohen-Salmon M
    J Neurosci; 2013 Jan; 33(2):430-4. PubMed ID: 23303923
    [TBL] [Abstract][Full Text] [Related]  

  • 38. In vivo genetic manipulation of inner ear connexin expression by bovine adeno-associated viral vectors.
    Crispino G; Galindo Ramirez F; Campioni M; Zorzi V; Praetorius M; Di Pasquale G; Chiorini JA; Mammano F
    Sci Rep; 2017 Aug; 7(1):6567. PubMed ID: 28779115
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Using assessment of higher brain functions of children with GJB2-associated deafness and cochlear implants as a procedure to evaluate language development.
    Kawasaki A; Fukushima K; Kataoka Y; Fukuda S; Nishizaki K
    Int J Pediatr Otorhinolaryngol; 2006 Aug; 70(8):1343-9. PubMed ID: 16549217
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Residual Hearing in DFNB1 Deafness and Its Clinical Implication in a Korean Population.
    Kim SY; Kim AR; Han KH; Kim MY; Jeon EH; Koo JW; Oh SH; Choi BY
    PLoS One; 2015; 10(6):e0125416. PubMed ID: 26061264
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.