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 *

190 related articles for article (PubMed ID: 26749107)

  • 1. The pathological effects of connexin 26 variants related to hearing loss by in silico and in vitro analysis.
    Kim HR; Oh SK; Lee ES; Choi SY; Roh SE; Kim SJ; Tsukihara T; Lee KY; Jeon CJ; Kim UK
    Hum Genet; 2016 Mar; 135(3):287-98. PubMed ID: 26749107
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Different functional consequences of two missense mutations in the GJB2 gene associated with non-syndromic hearing loss.
    Choi SY; Park HJ; Lee KY; Dinh EH; Chang Q; Ahmad S; Lee SH; Bok J; Lin X; Kim UK
    Hum Mutat; 2009 Jul; 30(7):E716-27. PubMed ID: 19384972
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in the gene for connexin 26 (GJB2) that cause hearing loss have a dominant negative effect on connexin 30.
    Marziano NK; Casalotti SO; Portelli AE; Becker DL; Forge A
    Hum Mol Genet; 2003 Apr; 12(8):805-12. PubMed ID: 12668604
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Induction of cell death and gain-of-function properties of connexin26 mutants predict severity of skin disorders and hearing loss.
    Press ER; Shao Q; Kelly JJ; Chin K; Alaga A; Laird DW
    J Biol Chem; 2017 Jun; 292(23):9721-9732. PubMed ID: 28428247
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel mechanism for connexin 26 mutation linked deafness: cell death caused by leaky gap junction hemichannels.
    Stong BC; Chang Q; Ahmad S; Lin X
    Laryngoscope; 2006 Dec; 116(12):2205-10. PubMed ID: 17146396
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Gap-junction channels dysfunction in deafness and hearing loss.
    Martínez AD; Acuña R; Figueroa V; Maripillan J; Nicholson B
    Antioxid Redox Signal; 2009 Feb; 11(2):309-22. PubMed ID: 18837651
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dominant Cx26 mutants associated with hearing loss have dominant-negative effects on wild type Cx26.
    Zhang J; Scherer SS; Yum SW
    Mol Cell Neurosci; 2011 Jun; 47(2):71-8. PubMed ID: 21040787
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Connexin Type and Fluorescent Protein Fusion Tag Determine Structural Stability of Gap Junction Plaques.
    Stout RF; Snapp EL; Spray DC
    J Biol Chem; 2015 Sep; 290(39):23497-514. PubMed ID: 26265468
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Functional analysis of connexin-26 mutants associated with hereditary recessive deafness.
    Wang HL; Chang WT; Li AH; Yeh TH; Wu CY; Chen MS; Huang PC
    J Neurochem; 2003 Feb; 84(4):735-42. PubMed ID: 12562518
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Connexins in hearing loss: a comprehensive overview.
    Sabag AD; Dagan O; Avraham KB
    J Basic Clin Physiol Pharmacol; 2005; 16(2-3):101-16. PubMed ID: 16285463
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Functional evaluation of GJB2 variants in nonsyndromic hearing loss.
    Choi SY; Lee KY; Kim HJ; Kim HK; Chang Q; Park HJ; Jeon CJ; Lin X; Bok J; Kim UK
    Mol Med; 2011; 17(5-6):550-6. PubMed ID: 21298213
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30.
    Yum SW; Zhang J; Scherer SS
    Neurobiol Dis; 2010 May; 38(2):226-36. PubMed ID: 20096356
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Engineered Cx26 variants established functional heterotypic Cx26/Cx43 and Cx26/Cx40 gap junction channels.
    Karademir LB; Aoyama H; Yue B; Chen H; Bai D
    Biochem J; 2016 May; 473(10):1391-403. PubMed ID: 26987811
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evaluation of the pathogenicity of GJB3 and GJB6 variants associated with nonsyndromic hearing loss.
    Oh SK; Choi SY; Yu SH; Lee KY; Hong JH; Hur SW; Kim SJ; Jeon CJ; Kim UK
    Biochim Biophys Acta; 2013 Jan; 1832(1):285-91. PubMed ID: 22617145
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Gap junctions in the inner ear: comparison of distribution patterns in different vertebrates and assessement of connexin composition in mammals.
    Forge A; Becker D; Casalotti S; Edwards J; Marziano N; Nevill G
    J Comp Neurol; 2003 Dec; 467(2):207-31. PubMed ID: 14595769
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A deafness mechanism of digenic Cx26 (GJB2) and Cx30 (GJB6) mutations: Reduction of endocochlear potential by impairment of heterogeneous gap junctional function in the cochlear lateral wall.
    Mei L; Chen J; Zong L; Zhu Y; Liang C; Jones RO; Zhao HB
    Neurobiol Dis; 2017 Dec; 108():195-203. PubMed ID: 28823936
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deficient membrane integration of the novel p.N14D-GJB2 mutant associated with non-syndromic hearing impairment.
    Haack B; Schmalisch K; Palmada M; Böhmer C; Kohlschmidt N; Keilmann A; Zechner U; Limberger A; Beckert S; Zenner HP; Lang F; Kupka S
    Hum Mutat; 2006 Nov; 27(11):1158-9. PubMed ID: 17041897
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Impaired gap junctions in human hepatocellular carcinoma limit intrinsic oxaliplatin chemosensitivity: A key role of connexin 26.
    Yang Y; Zhu J; Zhang N; Zhao Y; Li WY; Zhao FY; Ou YR; Qin SK; Wu Q
    Int J Oncol; 2016 Feb; 48(2):703-13. PubMed ID: 26648344
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The p.Cys169Tyr variant of connexin 26 is not a polymorphism.
    Zonta F; Girotto G; Buratto D; Crispino G; Morgan A; Abdulhadi K; Alkowari M; Badii R; Gasparini P; Mammano F
    Hum Mol Genet; 2015 May; 24(9):2641-8. PubMed ID: 25628337
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.