203 related articles for article (PubMed ID: 31988333)
21. In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca
Fukunaga I; Fujimoto A; Hatakeyama K; Aoki T; Nishikawa A; Noda T; Minowa O; Kurebayashi N; Ikeda K; Kamiya K
Stem Cell Reports; 2016 Dec; 7(6):1023-1036. PubMed ID: 27840044
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Modeling gap junction beta 2 gene-related deafness with human iPSC.
Fukunaga I; Oe Y; Danzaki K; Ohta S; Chen C; Shirai K; Kawano A; Ikeda K; Kamiya K
Hum Mol Genet; 2021 Jul; 30(15):1429-1442. PubMed ID: 33997905
[TBL] [Abstract][Full Text] [Related]
24. Cochlear gap junctions coassembled from Cx26 and 30 show faster intercellular Ca2+ signaling than homomeric counterparts.
Sun J; Ahmad S; Chen S; Tang W; Zhang Y; Chen P; Lin X
Am J Physiol Cell Physiol; 2005 Mar; 288(3):C613-23. PubMed ID: 15692151
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. 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]
27. 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]
28. Actin-independent trafficking of cochlear connexin 26 to non-lipid raft gap junction plaques.
Defourny J; Thelen N; Thiry M
Hear Res; 2019 Mar; 374():69-75. PubMed ID: 30732922
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. 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]
31. Generation of Functional CX26-Gap-Junction-Plaque-Forming Cells with Spontaneous Ca
Fukunaga I; Fujimoto A; Hatakeyama K; Kurebayashi N; Ikeda K; Kamiya K
Curr Protoc Stem Cell Biol; 2019 Dec; 51(1):e100. PubMed ID: 31756039
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Connexin hemichannels and cochlear function.
Verselis VK
Neurosci Lett; 2019 Mar; 695():40-45. PubMed ID: 28917982
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. 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]
36. 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]
37. Pannexin 1 deficiency can induce hearing loss.
Zhao HB; Zhu Y; Liang C; Chen J
Biochem Biophys Res Commun; 2015 Jul 17-24; 463(1-2):143-7. PubMed ID: 26002464
[TBL] [Abstract][Full Text] [Related]
38. Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death.
Cohen-Salmon M; Ott T; Michel V; Hardelin JP; Perfettini I; Eybalin M; Wu T; Marcus DC; Wangemann P; Willecke K; Petit C
Curr Biol; 2002 Jul; 12(13):1106-11. PubMed ID: 12121617
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. 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]
[Previous] [Next] [New Search]
