AAAAAA

   
Results: 1-9 |
Results: 9

Authors: Qu, W Moorhouse, AJ Cunningham, AM Barry, PH
Citation: W. Qu et al., Anomalous mole-fraction effects in recombinant and native cyclic nucleotide-gated channels in rat olfactory receptor neurons, P ROY SOC B, 268(1474), 2001, pp. 1395-1403

Authors: Kaur, R Zhu, XO Moorhouse, AJ Barry, PH
Citation: R. Kaur et al., IP3-gated channels and their occurrence relative to CNG channels in the soma and dendritic knob of rat olfactory receptor neurons, J MEMBR BIO, 181(2), 2001, pp. 91-105

Authors: Friedrich, O Ehmer, T Uttenweiler, D Vogel, M Barry, PH Fink, RHA
Citation: O. Friedrich et al., Numerical analysis of Ca2+ depletion in the transverse tubular system of mammalian muscle, BIOPHYS J, 80(5), 2001, pp. 2046-2055

Authors: Qu, W Zhu, XO Moorhouse, AJ Bieri, S Cunningham, AM Barry, PH
Citation: W. Qu et al., Ion permeation and selectivity of wild-type recombinant rat CNG (rOCNC1) channels expressed in HEK293 cells, J MEMBR BIO, 178(2), 2000, pp. 137-150

Authors: Qu, W Moorhouse, AJ Rajendra, S Barry, PH
Citation: W. Qu et al., Very negative potential for half-inactivation of, and effects of anions on, voltage-dependent sodium currents in acutely isolated rat olfactory receptor neurons, J MEMBR BIO, 175(2), 2000, pp. 123-138

Authors: Keramidas, A Moorhouse, AJ French, CR Schofield, PR Barry, PH
Citation: A. Keramidas et al., M2 pore mutations convert the glycine receptor channel from being anion- to cation-selective, BIOPHYS J, 79(1), 2000, pp. 247-259

Authors: Barry, PH Schofield, PR Moorhouse, AJ
Citation: Ph. Barry et al., Glycine receptors: What gets in and why?, CLIN EXP PH, 26(11), 1999, pp. 935-936

Authors: Keramidas, A Kuhlmann, L Moorhouse, AJ Barry, PH
Citation: A. Keramidas et al., Measurement of the limiting equivalent conductivities and mobilities of the most prevalent ionic species of EGTA (EGTA(2-) and EGTA(3-)) for use in electrophysiological experiments, J NEUROSC M, 89(1), 1999, pp. 41-47

Authors: Moorhouse, AJ Jacques, P Barry, PH Schofield, PR
Citation: Aj. Moorhouse et al., The startle disease mutation Q266H, in the second transmembrane domain of the human glycine receptor, impairs channel gating, MOLEC PHARM, 55(2), 1999, pp. 386-395
Risultati: 1-9 |