Lucia Sivilotti

University College London, London, United Kingdom 
"Lucia Sivilotti"
Mean distance: 16.79 (cluster 11)


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katarzyna d. bera research assistant UCL
Marabelli Alessandro grad student UCL (Physiology Academic Tree)
steven broadbent grad student
Marco Beato post-doc UCL
Antonios Pantazis post-doc 2006-2008 UCL


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Philip Biggin collaborator UCL
David Colquhoun collaborator UCL
Clifford Woolf collaborator UCL
Trevor M. Lewis collaborator 1994-1997 UCL
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Wu Z, Lape R, Jopp-Saile L, et al. (2020) The Startle disease mutation, α1S270T, predicts shortening of glycinergic synaptic currents. The Journal of Physiology
Ivica J, Lape R, Jazbec V, et al. (2020) The intracellular domain of homomeric glycine receptors modulates agonist efficacy. The Journal of Biological Chemistry
Safar F, Hurdiss E, Erotocritou M, et al. (2017) The startle disease mutation E103K impairs activation of human homomeric α1 glycine receptors by disrupting an intersubunit salt bridge across the agonist binding site. The Journal of Biological Chemistry
Groot-Kormelink PJ, Ferrand S, Kelley N, et al. (2016) High Throughput Random Mutagenesis and Single Molecule Real Time Sequencing of the Muscle Nicotinic Acetylcholine Receptor. Plos One. 11: e0163129
Epstein M, Calderhead B, Girolami MA, et al. (2016) Bayesian Statistical Inference in Ion-Channel Models with Exact Missed Event Correction. Biophysical Journal. 111: 333-48
Sivilotti L, Colquhoun D. (2016) In praise of single channel kinetics. The Journal of General Physiology
Marabelli A, Lape R, Sivilotti L. (2015) Mechanism of activation of the prokaryotic channel ELIC by propylamine: a single-channel study. The Journal of General Physiology. 145: 23-45
Yu R, Hurdiss E, Greiner T, et al. (2014) Agonist and antagonist binding in human glycine receptors. Biochemistry. 53: 6041-51
Calderhead B, Epstein M, Sivilotti L, et al. (2013) Bayesian approaches for mechanistic ion channel modeling. Methods in Molecular Biology (Clifton, N.J.). 1021: 247-72
Marabelli A, Moroni M, Lape R, et al. (2013) The kinetic properties of the α3 rat glycine receptor make it suitable for mediating fast synaptic inhibition. The Journal of Physiology. 591: 3289-308
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