239 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]
