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.
301 related articles for article (PubMed ID: 24225640)
1. Virally expressed connexin26 restores gap junction function in the cochlea of conditional Gjb2 knockout mice. Yu Q; Wang Y; Chang Q; Wang J; Gong S; Li H; Lin X Gene Ther; 2014 Jan; 21(1):71-80. PubMed ID: 24225640 [TBL] [Abstract][Full Text] [Related]
2. 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]
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. 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]
5. Connexin 26 null mice exhibit spiral ganglion degeneration that can be blocked by BDNF gene therapy. Takada Y; Beyer LA; Swiderski DL; O'Neal AL; Prieskorn DM; Shivatzki S; Avraham KB; Raphael Y Hear Res; 2014 Mar; 309():124-35. PubMed ID: 24333301 [TBL] [Abstract][Full Text] [Related]
6. Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness. Iizuka T; Kamiya K; Gotoh S; Sugitani Y; Suzuki M; Noda T; Minowa O; Ikeda K Hum Mol Genet; 2015 Jul; 24(13):3651-61. PubMed ID: 25801282 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness. Kudo T; Kure S; Ikeda K; Xia AP; Katori Y; Suzuki M; Kojima K; Ichinohe A; Suzuki Y; Aoki Y; Kobayashi T; Matsubara Y Hum Mol Genet; 2003 May; 12(9):995-1004. PubMed ID: 12700168 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. Connexin32 can restore hearing in connexin26 deficient mice. Degen J; Schütz M; Dicke N; Strenzke N; Jokwitz M; Moser T; Willecke K Eur J Cell Biol; 2011 Oct; 90(10):817-24. PubMed ID: 21813206 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. 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] [Next] [New Search]