John J. Kelly - Publications
Affiliations: | 2008-2011 | Ear Institute | University College London, London, United Kingdom |
Year | Citation | Score | |||
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2015 | Kelly JJ, Shao Q, Jagger DJ, Laird DW. Cx30 exhibits unique characteristics including a long half-life when assembled into gap junctions. Journal of Cell Science. PMID 26359304 DOI: 10.1242/Jcs.174698 | 0.486 | |||
2014 | Chen J, Ingham N, Kelly J, Jadeja S, Goulding D, Pass J, Mahajan VB, Tsang SH, Nijnik A, Jackson IJ, White JK, Forge A, Jagger D, Steel KP. Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss. Plos Genetics. 10: e1004688. PMID 25356849 DOI: 10.1371/Journal.Pgen.1004688 | 0.499 | |||
2013 | Forge A, Jagger DJ, Kelly JJ, Taylor RR. Connexin30-mediated intercellular communication plays an essential role in epithelial repair in the cochlea. Journal of Cell Science. 126: 1703-12. PMID 23424196 DOI: 10.1242/Jcs.125476 | 0.495 | |||
2012 | Kelly JJ, Forge A, Jagger DJ. Contractility in type III cochlear fibrocytes is dependent on non-muscle myosin II and intercellular gap junctional coupling. Journal of the Association For Research in Otolaryngology : Jaro. 13: 473-84. PMID 22476723 DOI: 10.1007/S10162-012-0322-7 | 0.486 | |||
2011 | Jagger D, Collin G, Kelly J, Towers E, Nevill G, Longo-Guess C, Benson J, Halsey K, Dolan D, Marshall J, Naggert J, Forge A. Alström Syndrome protein ALMS1 localizes to basal bodies of cochlear hair cells and regulates cilium-dependent planar cell polarity. Human Molecular Genetics. 20: 466-81. PMID 21071598 DOI: 10.1093/Hmg/Ddq493 | 0.491 | |||
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