BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

252 related articles for article (PubMed ID: 24732355)

  • 1. Deafness induced by Connexin 26 (GJB2) deficiency is not determined by endocochlear potential (EP) reduction but is associated with cochlear developmental disorders.
    Chen J; Chen J; Zhu Y; Liang C; Zhao HB
    Biochem Biophys Res Commun; 2014 May; 448(1):28-32. PubMed ID: 24732355
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cell degeneration is not a primary causer for Connexin26 (GJB2) deficiency associated hearing loss.
    Liang C; Zhu Y; Zong L; Lu GJ; Zhao HB
    Neurosci Lett; 2012 Oct; 528(1):36-41. PubMed ID: 22975134
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Timed conditional null of connexin26 in mice reveals temporary requirements of connexin26 in key cochlear developmental events before the onset of hearing.
    Chang Q; Tang W; Kim Y; Lin X
    Neurobiol Dis; 2015 Jan; 73():418-27. PubMed ID: 25251605
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Connexin26 gap junction mediates miRNA intercellular genetic communication in the cochlea and is required for inner ear development.
    Zhu Y; Zong L; Mei L; Zhao HB
    Sci Rep; 2015 Oct; 5():15647. PubMed ID: 26490746
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Deficiency of transcription factor Brn4 disrupts cochlear gap junction plaques in a model of DFN3 non-syndromic deafness.
    Kidokoro Y; Karasawa K; Minowa O; Sugitani Y; Noda T; Ikeda K; Kamiya K
    PLoS One; 2014; 9(9):e108216. PubMed ID: 25259580
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Degradation of cochlear Connexin26 accelerate the development of age-related hearing loss.
    Xu K; Chen S; Bai X; Xie L; Qiu Y; Liu XZ; Wang XH; Kong WJ; Sun Y
    Aging Cell; 2023 Nov; 22(11):e13973. PubMed ID: 37681746
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Assembly of the cochlear gap junction macromolecular complex requires connexin 26.
    Kamiya K; Yum SW; Kurebayashi N; Muraki M; Ogawa K; Karasawa K; Miwa A; Guo X; Gotoh S; Sugitani Y; Yamanaka H; Ito-Kawashima S; Iizuka T; Sakurai T; Noda T; Minowa O; Ikeda K
    J Clin Invest; 2014 Apr; 124(4):1598-607. PubMed ID: 24590285
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Early developmental expression of connexin26 in the cochlea contributes to its dominate functional role in the cochlear gap junctions.
    Qu Y; Tang W; Zhou B; Ahmad S; Chang Q; Li X; Lin X
    Biochem Biophys Res Commun; 2012 Jan; 417(1):245-50. PubMed ID: 22142852
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The protective effects of systemic dexamethasone on sensory epithelial damage and hearing loss in targeted Cx26-null mice.
    Xu K; Chen S; Xie L; Qiu Y; Liu XZ; Bai X; Jin Y; Wang XH; Sun Y
    Cell Death Dis; 2022 Jun; 13(6):545. PubMed ID: 35688810
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mice with conditional deletion of Cx26 exhibit no vestibular phenotype despite secondary loss of Cx30 in the vestibular end organs.
    Lee MY; Takada T; Takada Y; Kappy MD; Beyer LA; Swiderski DL; Godin AL; Brewer S; King WM; Raphael Y
    Hear Res; 2015 Oct; 328():102-12. PubMed ID: 26232528
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Expression of connexin 26 in the lateral wall of the rat cochlea after acoustic trauma.
    Hsu WC; Wang JD; Hsu CJ; Lee SY; Yeh TH
    Acta Otolaryngol; 2004 May; 124(4):459-63. PubMed ID: 15224875
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss - A Common Hereditary Deafness.
    Wingard JC; Zhao HB
    Front Cell Neurosci; 2015; 9():202. PubMed ID: 26074771
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hypothesis of K
    Zhao HB
    Front Mol Neurosci; 2017; 10():162. PubMed ID: 28603488
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ultrastructural pathological changes in the cochlear cells of connexin 26 conditional knockout mice.
    Lin L; Wang YF; Wang SY; Liu SF; Yu Z; Xi L; Li HW
    Mol Med Rep; 2013 Oct; 8(4):1029-36. PubMed ID: 23917463
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Reduced postnatal expression of cochlear Connexin26 induces hearing loss and affects the developmental status of pillar cells in a dose-dependent manner.
    Xie L; Chen S; Xu K; Cao HY; Du AN; Bai X; Sun Y; Kong WJ
    Neurochem Int; 2019 Sep; 128():196-205. PubMed ID: 31034913
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Progressive age-dependence and frequency difference in the effect of gap junctions on active cochlear amplification and hearing.
    Zong L; Chen J; Zhu Y; Zhao HB
    Biochem Biophys Res Commun; 2017 Jul; 489(2):223-227. PubMed ID: 28552523
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Reduced electromotility of outer hair cells associated with connexin-related forms of deafness: an in silico study of a cochlear network mechanism.
    Mistrík P; Ashmore JF
    J Assoc Res Otolaryngol; 2010 Dec; 11(4):559-71. PubMed ID: 20635191
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Connexin-Mediated Signaling in Nonsensory Cells Is Crucial for the Development of Sensory Inner Hair Cells in the Mouse Cochlea.
    Johnson SL; Ceriani F; Houston O; Polishchuk R; Polishchuk E; Crispino G; Zorzi V; Mammano F; Marcotti W
    J Neurosci; 2017 Jan; 37(2):258-268. PubMed ID: 28077706
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.