188 related articles for article (PubMed ID: 17420259)
1. Differential potency of dominant negative connexin43 mutants in oculodentodigital dysplasia.
Gong XQ; Shao Q; Langlois S; Bai D; Laird DW
J Biol Chem; 2007 Jun; 282(26):19190-202. PubMed ID: 17420259
[TBL] [Abstract][Full Text] [Related]
2. Oculodentodigital dysplasia-causing connexin43 mutants are non-functional and exhibit dominant effects on wild-type connexin43.
Roscoe W; Veitch GI; Gong XQ; Pellegrino E; Bai D; McLachlan E; Shao Q; Kidder GM; Laird DW
J Biol Chem; 2005 Mar; 280(12):11458-66. PubMed ID: 15644317
[TBL] [Abstract][Full Text] [Related]
3. Functional characterization of oculodentodigital dysplasia-associated Cx43 mutants.
McLachlan E; Manias JL; Gong XQ; Lounsbury CS; Shao Q; Bernier SM; Bai D; Laird DW
Cell Commun Adhes; 2005; 12(5-6):279-92. PubMed ID: 16531323
[TBL] [Abstract][Full Text] [Related]
4. Functional characterization of a GJA1 frameshift mutation causing oculodentodigital dysplasia and palmoplantar keratoderma.
Gong XQ; Shao Q; Lounsbury CS; Bai D; Laird DW
J Biol Chem; 2006 Oct; 281(42):31801-11. PubMed ID: 16891658
[TBL] [Abstract][Full Text] [Related]
5. Autosomal recessive GJA1 (Cx43) gene mutations cause oculodentodigital dysplasia by distinct mechanisms.
Huang T; Shao Q; MacDonald A; Xin L; Lorentz R; Bai D; Laird DW
J Cell Sci; 2013 Jul; 126(Pt 13):2857-66. PubMed ID: 23606748
[TBL] [Abstract][Full Text] [Related]
6. Oculodentodigital dysplasia connexin43 mutations result in non-functional connexin hemichannels and gap junctions in C6 glioma cells.
Lai A; Le DN; Paznekas WA; Gifford WD; Jabs EW; Charles AC
J Cell Sci; 2006 Feb; 119(Pt 3):532-41. PubMed ID: 16418219
[TBL] [Abstract][Full Text] [Related]
7. Functional characterization of connexin43 mutations found in patients with oculodentodigital dysplasia.
Shibayama J; Paznekas W; Seki A; Taffet S; Jabs EW; Delmar M; Musa H
Circ Res; 2005 May; 96(10):e83-91. PubMed ID: 15879313
[TBL] [Abstract][Full Text] [Related]
8. Some oculodentodigital dysplasia-associated Cx43 mutations cause increased hemichannel activity in addition to deficient gap junction channels.
Dobrowolski R; Sommershof A; Willecke K
J Membr Biol; 2007 Oct; 219(1-3):9-17. PubMed ID: 17687502
[TBL] [Abstract][Full Text] [Related]
9. Fate of connexin43 in cardiac tissue harbouring a disease-linked connexin43 mutant.
Manias JL; Plante I; Gong XQ; Shao Q; Churko J; Bai D; Laird DW
Cardiovasc Res; 2008 Dec; 80(3):385-95. PubMed ID: 18678643
[TBL] [Abstract][Full Text] [Related]
10. Structure and functional studies of N-terminal Cx43 mutants linked to oculodentodigital dysplasia.
Shao Q; Liu Q; Lorentz R; Gong XQ; Bai D; Shaw GS; Laird DW
Mol Biol Cell; 2012 Sep; 23(17):3312-21. PubMed ID: 22809623
[TBL] [Abstract][Full Text] [Related]
11. Manipulating Cx43 expression triggers gene reprogramming events in dermal fibroblasts from oculodentodigital dysplasia patients.
Esseltine JL; Shao Q; Huang T; Kelly JJ; Sampson J; Laird DW
Biochem J; 2015 Nov; 472(1):55-69. PubMed ID: 26349540
[TBL] [Abstract][Full Text] [Related]
12. Specific functional pathologies of Cx43 mutations associated with oculodentodigital dysplasia.
Kelly JJ; Esseltine JL; Shao Q; Jabs EW; Sampson J; Auranen M; Bai D; Laird DW
Mol Biol Cell; 2016 Jul; 27(14):2172-85. PubMed ID: 27226478
[TBL] [Abstract][Full Text] [Related]
13. ODDD-linked Cx43 mutants reduce endogenous Cx43 expression and function in osteoblasts and inhibit late stage differentiation.
McLachlan E; Plante I; Shao Q; Tong D; Kidder GM; Bernier SM; Laird DW
J Bone Miner Res; 2008 Jun; 23(6):928-38. PubMed ID: 18269311
[TBL] [Abstract][Full Text] [Related]
14. Cerebral ischemic injury is enhanced in a model of oculodentodigital dysplasia.
Kozoriz MG; Lai S; Vega JL; Sáez JC; Sin WC; Bechberger JF; Naus CC
Neuropharmacology; 2013 Dec; 75():549-56. PubMed ID: 23727526
[TBL] [Abstract][Full Text] [Related]
15. Myogenic bladder defects in mouse models of human oculodentodigital dysplasia.
Huang T; Shao Q; Barr K; Simek J; Fishman GI; Laird DW
Biochem J; 2014 Feb; 457(3):441-9. PubMed ID: 24228978
[TBL] [Abstract][Full Text] [Related]
16. A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
Flenniken AM; Osborne LR; Anderson N; Ciliberti N; Fleming C; Gittens JE; Gong XQ; Kelsey LB; Lounsbury C; Moreno L; Nieman BJ; Peterson K; Qu D; Roscoe W; Shao Q; Tong D; Veitch GI; Voronina I; Vukobradovic I; Wood GA; Zhu Y; Zirngibl RA; Aubin JE; Bai D; Bruneau BG; Grynpas M; Henderson JE; Henkelman RM; McKerlie C; Sled JG; Stanford WL; Laird DW; Kidder GM; Adamson SL; Rossant J
Development; 2005 Oct; 132(19):4375-86. PubMed ID: 16155213
[TBL] [Abstract][Full Text] [Related]
17. Oogenesis defects in a mutant mouse model of oculodentodigital dysplasia.
Tong D; Colley D; Thoo R; Li TY; Plante I; Laird DW; Bai D; Kidder GM
Dis Model Mech; 2009; 2(3-4):157-67. PubMed ID: 19259389
[TBL] [Abstract][Full Text] [Related]
18. The potency of the fs260 connexin43 mutant to impair keratinocyte differentiation is distinct from other disease-linked connexin43 mutants.
Churko JM; Langlois S; Pan X; Shao Q; Laird DW
Biochem J; 2010 Aug; 429(3):473-83. PubMed ID: 20515445
[TBL] [Abstract][Full Text] [Related]
19. Effects of reduced connexin43 function on skull development in the Cx43
Jarvis SE; Lee JE; Jewlal E; Barr K; Kelly GM; Laird DW; Willmore KE
Bone; 2020 Jul; 136():115365. PubMed ID: 32320893
[TBL] [Abstract][Full Text] [Related]
20. The severity of mammary gland developmental defects is linked to the overall functional status of Cx43 as revealed by genetically modified mice.
Stewart MK; Gong XQ; Barr KJ; Bai D; Fishman GI; Laird DW
Biochem J; 2013 Jan; 449(2):401-13. PubMed ID: 23075222
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
