Chris Shelley - Publications

Affiliations: 
2014- Franklin and Marshall College, Lancaster, PA, United States 
Area:
Single ion channels, AMPA receptors

13 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2013 Shelley C, Whitt JP, Montgomery JR, Meredith AL. Phosphorylation of a constitutive serine inhibits BK channel variants containing the alternate exon "SRKR". The Journal of General Physiology. 142: 585-98. PMID 24277602 DOI: 10.1085/jgp.201311072  1
2012 Shelley C, Farrant M, Cull-Candy SG. TARP-associated AMPA receptors display an increased maximum channel conductance and multiple kinetically distinct open states. The Journal of Physiology. 590: 5723-38. PMID 22988139 DOI: 10.1113/jphysiol.2012.238006  1
2012 Coombs ID, Soto D, Zonouzi M, Renzi M, Shelley C, Farrant M, Cull-Candy SG. Cornichons modify channel properties of recombinant and glial AMPA receptors. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 9796-804. PMID 22815494 DOI: 10.1523/JNEUROSCI.0345-12.2012  1
2010 Shelley C, Cull-Candy SG. Desensitization and models of receptor-channel activation. The Journal of Physiology. 588: 1395-7. PMID 20436045 DOI: 10.1113/jphysiol.2010.188664  1
2010 Shelley C, Niu X, Geng Y, Magleby KL. Coupling and cooperativity in voltage activation of a limited-state BK channel gating in saturating Ca2+. The Journal of General Physiology. 135: 461-80. PMID 20421372 DOI: 10.1085/jgp.200910331  1
2009 Croxen R, Hatton C, Shelley C, Brydson M, Chauplannaz G, Oosterhuis H, Vincent A, Newsom-Davis J, Colquhoun D, Beeson D. Voluntary partial retraction of: Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes. Neurology. 72: 294. PMID 19153382 DOI: 10.1212/01.wnl.0000344248.36823.b5  1
2008 Shelley C, Magleby KL. Linking exponential components to kinetic states in Markov models for single-channel gating. The Journal of General Physiology. 132: 295-312. PMID 18625850 DOI: 10.1085/jgp.200810008  1
2008 Shelley C, Colquhoun D. Corrigendum to A human congenital myasthenia-causing-mutation (eL78P) of the muscle nicotinic acetylcholine receptor with unusual single channel properties [J Physiol (2005) 564, 377-396] Journal of Physiology. 586: 5277-5277. DOI: 10.1113/jphysiol.2008.162628  1
2006 Mishra SH, Shelley CM, Barrow DJ, Darby MK, Germann MW. Solution structures and characterization of human immunodeficiency virus Rev responsive element IIB RNA targeting zinc finger proteins. Biopolymers. 83: 352-64. PMID 16826557 DOI: 10.1002/bip.20565  1
2005 Shelley C, Colquhoun D. A human congenital myasthenia-causing mutation (epsilon L78P) of the muscle nicotinic acetylcholine receptor with unusual single channel properties. The Journal of Physiology. 564: 377-96. PMID 15731194 DOI: 10.1113/jphysiol.2004.081497  1
2003 Beeson D, Webster R, Ealing J, Croxen R, Brownlow S, Brydson M, Newsom-Davis J, Slater C, Hatton C, Shelley C, Colquhoun D, Vincent A. Structural abnormalities of the AChR caused by mutations underlying congenital myasthenic syndromes. Annals of the New York Academy of Sciences. 998: 114-24. PMID 14592868 DOI: 10.1196/annals.1254.013  1
2003 Hatton CJ, Shelley C, Brydson M, Beeson D, Colquhoun D. Properties of the human muscle nicotinic receptor, and of the slow-channel myasthenic syndrome mutant epsilonL221F, inferred from maximum likelihood fits. The Journal of Physiology. 547: 729-60. PMID 12562900 DOI: 10.1113/jphysiol.2002.034173  1
2002 Croxen R, Hatton C, Shelley C, Brydson M, Chauplannaz G, Oosterhuis H, Vincent A, Newsom-Davis J, Colquhoun D, Beeson D. Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes. Neurology. 59: 162-8. PMID 12141316  1
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