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Journal of Neurochemistry|December 1, 1987
Effects of nucleus basalis lesions on the muscarinic and nicotinic modulation of [3H]acetylcholine release in the rat cerebral cortexE M Meyer, G W Arendash, J H Judkins, et al.Biochemistry|December 24, 1996
An essential binding surface for ShK toxin interaction with rat brain potassium channelsM W Pennington, V M Mahnir, I Khaytin, et al.Neuroscience Letters|February 28, 1994
A novel nicotinic agonist facilitates induction of long-term potentiation in the rat hippocampusB E Hunter, C M de Fiebre, R L Papke, et al.Biochimica Et Biophysica Acta|January 4, 1996
Synthesis and structural characterisation of analogues of the potassium channel blocker charybdotoxinT R Dyke, B M Duggan, M W Pennington, et al.FEBS Letters|March 7, 1983
Cobra polypeptide cytotoxin I and marine worm polypeptide cytotoxin A-IV are potent and selective inhibitors of phospholipid-sensitive Ca2+-dependent protein kinaseJ F Kuo, R L Raynor, G J Mazzei, et al.Molecular Pharmacology|January 1, 1995
Characterization of a series of anabaseine-derived compounds reveals that the 3-(4)-dimethylaminocinnamylidine derivative is a selective agonist at neuronal nicotinic alpha 7/125I-alpha-bungarotoxin receptor subtypesC M de Fiebre, E M Meyer, J C Henry, et al.British Journal of Pharmacology|August 20, 2010
Neuroprotection by donepezil against glutamate excitotoxicity involves stimulation of alpha7 nicotinic receptors and internalization of NMDA receptorsH Shen, T Kihara, H Hongo, et al.Toxicon : Official Journal of the International Society on Toxinology|February 17, 2018
Complete inhibition of fetal movement in the day 40 pregnant goat model by the piperidine alkaloid anabasine but not related alkaloidsB T Green, S T Lee, J W Keele, et al.Biochimica Et Biophysica Acta|July 20, 1994
Limited proteolysis study of structure-function relationships in Sh I, a polypeptide neurotoxin from a sea anemoneS A Monks, A R Gould, P E Lumley, et al.Biochemical and Biophysical Research Communications|February 27, 1996
Identification of three separate binding sites on SHK toxin, a potent inhibitor of voltage-dependent potassium channels in human T-lymphocytes and rat brainM W Pennington, V M Mahnir, D S Krafte, et al.Pageof 6