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 *

234 related articles for article (PubMed ID: 20858605)

  • 1. The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice.
    Schütz M; Scimemi P; Majumder P; De Siati RD; Crispino G; Rodriguez L; Bortolozzi M; Santarelli R; Seydel A; Sonntag S; Ingham N; Steel KP; Willecke K; Mammano F
    Hum Mol Genet; 2010 Dec; 19(24):4759-73. PubMed ID: 20858605
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre mice.
    Crispino G; Di Pasquale G; Scimemi P; Rodriguez L; Galindo Ramirez F; De Siati RD; Santarelli RM; Arslan E; Bortolozzi M; Chiorini JA; Mammano F
    PLoS One; 2011; 6(8):e23279. PubMed ID: 21876744
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Human connexin26 and connexin30 form functional heteromeric and heterotypic channels.
    Yum SW; Zhang J; Valiunas V; Kanaporis G; Brink PR; White TW; Scherer SS
    Am J Physiol Cell Physiol; 2007 Sep; 293(3):C1032-48. PubMed ID: 17615163
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Gap junction mediated intercellular metabolite transfer in the cochlea is compromised in connexin30 null mice.
    Chang Q; Tang W; Ahmad S; Zhou B; Lin X
    PLoS One; 2008; 3(12):e4088. PubMed ID: 19116647
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unique expression of connexins in the human cochlea.
    Liu W; Boström M; Kinnefors A; Rask-Andersen H
    Hear Res; 2009 Apr; 250(1-2):55-62. PubMed ID: 19450429
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness.
    Ahmad S; Tang W; Chang Q; Qu Y; Hibshman J; Li Y; Söhl G; Willecke K; Chen P; Lin X
    Proc Natl Acad Sci U S A; 2007 Jan; 104(4):1337-41. PubMed ID: 17227867
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis-ichthyosis-deafness syndrome.
    Schütz M; Auth T; Gehrt A; Bosen F; Körber I; Strenzke N; Moser T; Willecke K
    Hum Mol Genet; 2011 Jan; 20(1):28-39. PubMed ID: 20926451
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gap junction-mediated intercellular biochemical coupling in cochlear supporting cells is required for normal cochlear functions.
    Zhang Y; Tang W; Ahmad S; Sipp JA; Chen P; Lin X
    Proc Natl Acad Sci U S A; 2005 Oct; 102(42):15201-6. PubMed ID: 16217030
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. The inner ear contains heteromeric channels composed of cx26 and cx30 and deafness-related mutations in cx26 have a dominant negative effect on cx30.
    Forge A; Marziano NK; Casalotti SO; Becker DL; Jagger D
    Cell Commun Adhes; 2003; 10(4-6):341-6. PubMed ID: 14681039
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Functional studies reveal new mechanisms for deafness caused by connexin mutations.
    Chang Q; Tang W; Ahmad S; Stong B; Leu G; Lin X
    Otol Neurotol; 2009 Feb; 30(2):237-40. PubMed ID: 19169135
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Conserved glycine at position 45 of major cochlear connexins constitutes a vital component of the Ca²⁺ sensor for gating of gap junction hemichannels.
    Zhang Y; Hao H
    Biochem Biophys Res Commun; 2013 Jul; 436(3):424-9. PubMed ID: 23756814
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cochlear connexin 30 homomeric and heteromeric channels exhibit distinct assembly mechanisms.
    Defourny J; Thelen N; Thiry M
    Mech Dev; 2019 Feb; 155():8-14. PubMed ID: 30296578
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Recent insights into gap junction biogenesis in the cochlea.
    Defourny J; Thiry M
    Dev Dyn; 2023 Feb; 252(2):239-246. PubMed ID: 36106826
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.