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Cell and Tissue Research|November 16, 2014
Mechanisms linking connexin mutations to human diseasesJohn J Kelly, Jamie Simek, Dale W LairdThe Biochemical Journal|July 11, 2014
Pannexin channels and their links to human diseaseSilvia Penuela, Luke Harland, Jamie Simek, et al.Journal of Cell Science|January 29, 2009
Cx43 has distinct mobility within plasma-membrane domains, indicative of progressive formation of gap-junction plaquesJamie Simek, Jared Churko, Qing Shao, et al.Reproduction (Cambridge, England)|March 21, 2015
Insights into the role of connexins in mammary gland morphogenesis and functionMichael K G Stewart, Jamie Simek, Dale W LairdThe Biochemical Journal|November 16, 2013
Myogenic bladder defects in mouse models of human oculodentodigital dysplasiaTao Huang, Qing Shao, Kevin Barr, et al.Journal of Cell Science|September 15, 2005
Mechanisms of Cx43 and Cx26 transport to the plasma membrane and gap junction regenerationTamsin Thomas, Karen Jordan, Jamie Simek, et al.Journal of Cell Science|September 12, 2015
Cx30 exhibits unique characteristics including a long half-life when assembled into gap junctionsJohn J Kelly, Qing Shao, Daniel J Jagger, et al.Journal of Cell Science|February 14, 2014
Mutations in Cx30 that are linked to skin disease and non-syndromic hearing loss exhibit several distinct cellular pathologiesAmy C Berger, John J Kelly, Patrick Lajoie, et al.The Biochemical Journal|September 10, 2015
Manipulating Cx43 expression triggers gene reprogramming events in dermal fibroblasts from oculodentodigital dysplasia patientsJessica L Esseltine, Qing Shao, Tao Huang, et al.Journal of Cell Science|April 6, 2018
Mice harbouring an oculodentodigital dysplasia-linked Cx43 G60S mutation have severe hearing lossJulia M Abitbol, John J Kelly, Kevin J Barr, et al.Pageof 37