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.
128 related articles for article (PubMed ID: 34091987)
1. Connexin 43 contributes to phenotypic robustness of the mouse skull. Jewlal E; Barr K; Laird DW; Willmore KE Dev Dyn; 2021 Dec; 250(12):1810-1827. PubMed ID: 34091987 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Effects of Reduced Connexin43 Function on Mandibular Morphology and Osteogenesis in Mutant Mouse Models of Oculodentodigital Dysplasia. Moore AC; Wu J; Jewlal E; Barr K; Laird DW; Willmore KE Calcif Tissue Int; 2020 Dec; 107(6):611-624. PubMed ID: 32902679 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. Mice harbouring an oculodentodigital dysplasia-linked Cx43 G60S mutation have severe hearing loss. Abitbol JM; Kelly JJ; Barr KJ; Allman BL; Laird DW J Cell Sci; 2018 May; 131(9):. PubMed ID: 29618634 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Canalization and developmental stability in the Brachyrrhine mouse. Willmore KE; Zelditch ML; Young N; Ah-Seng A; Lozanoff S; HallgrÃmsson B J Anat; 2006 Mar; 208(3):361-72. PubMed ID: 16533318 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Discordant growth of nasal cartilage and bone contributes to phenotypic variability of the skull in a mouse model. Book SA; Moore AC; Tourigny MSG; Barr K; Willmore KE Dev Dyn; 2023 Jul; 252(7):1009-1025. PubMed ID: 36880689 [TBL] [Abstract][Full Text] [Related]