309 related articles for article (PubMed ID: 15914609)
1. In vivo and in vitro expression of connexins in the human corneal epithelium.
Shurman DL; Glazewski L; Gumpert A; Zieske JD; Richard G
Invest Ophthalmol Vis Sci; 2005 Jun; 46(6):1957-65. PubMed ID: 15914609
[TBL] [Abstract][Full Text] [Related]
2. Expression pattern of connexins in the corneal and limbal epithelium of a primate.
Yuan X; Chen Z; Yang Z; Gao J; Zhang A; Wu SM; Jacoby R
Cornea; 2009 Feb; 28(2):194-9. PubMed ID: 19158564
[TBL] [Abstract][Full Text] [Related]
3. Gap junctional communication in microinjected human limbal and peripheral corneal epithelial cells cultured on intact amniotic membrane.
Hernandez Galindo EE; Theiss C; Steuhl KP; Meller D
Exp Eye Res; 2003 Mar; 76(3):303-14. PubMed ID: 12573659
[TBL] [Abstract][Full Text] [Related]
4. Expression of the gap junction proteins connexin 26 and connexin 43 in human middle ear cholesteatoma.
Choung YH; Park K; Kang SO; Markov Raynov A; Ho Kim C; Choung PH
Acta Otolaryngol; 2006 Feb; 126(2):138-43. PubMed ID: 16428189
[TBL] [Abstract][Full Text] [Related]
5. Vitamin D receptor and metabolite effects on corneal epithelial cell gap junction proteins.
Lu X; Chen Z; Vick S; Watsky MA
Exp Eye Res; 2019 Oct; 187():107776. PubMed ID: 31465769
[TBL] [Abstract][Full Text] [Related]
6. Keratitis-ichthyosis-deafness syndrome-associated Cx26 mutants produce nonfunctional gap junctions but hyperactive hemichannels when co-expressed with wild type Cx43.
García IE; Maripillán J; Jara O; Ceriani R; Palacios-Muñoz A; Ramachandran J; Olivero P; Perez-Acle T; González C; Sáez JC; Contreras JE; Martínez AD
J Invest Dermatol; 2015 May; 135(5):1338-1347. PubMed ID: 25625422
[TBL] [Abstract][Full Text] [Related]
7. Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome.
Richard G; Rouan F; Willoughby CE; Brown N; Chung P; Ryynänen M; Jabs EW; Bale SJ; DiGiovanna JJ; Uitto J; Russell L
Am J Hum Genet; 2002 May; 70(5):1341-8. PubMed ID: 11912510
[TBL] [Abstract][Full Text] [Related]
8. The D50N mutation and syndromic deafness: altered Cx26 hemichannel properties caused by effects on the pore and intersubunit interactions.
Sanchez HA; Villone K; Srinivas M; Verselis VK
J Gen Physiol; 2013 Jul; 142(1):3-22. PubMed ID: 23797419
[TBL] [Abstract][Full Text] [Related]
9. Mechanisms of Cx43 and Cx26 transport to the plasma membrane and gap junction regeneration.
Thomas T; Jordan K; Simek J; Shao Q; Jedeszko C; Walton P; Laird DW
J Cell Sci; 2005 Oct; 118(Pt 19):4451-62. PubMed ID: 16159960
[TBL] [Abstract][Full Text] [Related]
10. Role for connexin 26 in metastasis of human malignant melanoma: communication between melanoma and endothelial cells via connexin 26.
Saito-Katsuragi M; Asada H; Niizeki H; Katoh F; Masuzawa M; Tsutsumi M; Kuniyasu H; Ito A; Nojima H; Miyagawa S
Cancer; 2007 Sep; 110(5):1162-72. PubMed ID: 17614106
[TBL] [Abstract][Full Text] [Related]
11. Intracellular domains of mouse connexin26 and -30 affect diffusional and electrical properties of gap junction channels.
Manthey D; Banach K; Desplantez T; Lee CG; Kozak CA; Traub O; Weingart R; Willecke K
J Membr Biol; 2001 May; 181(2):137-48. PubMed ID: 11420600
[TBL] [Abstract][Full Text] [Related]
12. Connexin expression patterns in the rat cornea: molecular evidence for communication compartments.
Laux-Fenton WT; Donaldson PJ; Kistler J; Green CR
Cornea; 2003 Jul; 22(5):457-64. PubMed ID: 12827052
[TBL] [Abstract][Full Text] [Related]
13. Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome.
Taki T; Takeichi T; Sugiura K; Akiyama M
Sci Rep; 2018 Aug; 8(1):12824. PubMed ID: 30150638
[TBL] [Abstract][Full Text] [Related]
14. Connexin 26 expression prevents down-regulation of barrier and fence functions of tight junctions by Na+/K+-ATPase inhibitor ouabain in human airway epithelial cell line Calu-3.
Go M; Kojima T; Takano K; Murata M; Koizumi J; Kurose M; Kamekura R; Osanai M; Chiba H; Spray DC; Himi T; Sawada N
Exp Cell Res; 2006 Nov; 312(19):3847-56. PubMed ID: 16982053
[TBL] [Abstract][Full Text] [Related]
15. Altered cellular localization and hemichannel activities of KID syndrome associated connexin26 I30N and D50Y mutations.
Aypek H; Bay V; Meşe G
BMC Cell Biol; 2016 Feb; 17():5. PubMed ID: 26831144
[TBL] [Abstract][Full Text] [Related]
16. Aberrant hemichannel properties of Cx26 mutations causing skin disease and deafness.
Gerido DA; DeRosa AM; Richard G; White TW
Am J Physiol Cell Physiol; 2007 Jul; 293(1):C337-45. PubMed ID: 17428836
[TBL] [Abstract][Full Text] [Related]
17. Reduction of malignant phenotype of HEPG2 cell is associated with the expression of connexin 26 but not connexin 32.
Yano T; Hernandez-Blazquez FJ; Omori Y; Yamasaki H
Carcinogenesis; 2001 Oct; 22(10):1593-600. PubMed ID: 11576997
[TBL] [Abstract][Full Text] [Related]
18. Asymmetric expression of connexins between luminal epithelial- and myoepithelial- cells is essential for contractile function of the mammary gland.
Mroue R; Inman J; Mott J; Budunova I; Bissell MJ
Dev Biol; 2015 Mar; 399(1):15-26. PubMed ID: 25500615
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Induction of cell death and gain-of-function properties of connexin26 mutants predict severity of skin disorders and hearing loss.
Press ER; Shao Q; Kelly JJ; Chin K; Alaga A; Laird DW
J Biol Chem; 2017 Jun; 292(23):9721-9732. PubMed ID: 28428247
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]