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Nature Neuroscience|April 9, 1999
Acetylcholine receptor M3 domain: stereochemical and volume contributions to channel gatingH L Wang, M Milone, K Ohno, et al.Neurology|July 13, 2005
Congenital endplate acetylcholinesterase deficiency responsive to ephedrineM Bestue-Cardiel, A Sáenz de Cabezón-Alvarez, J L Capablo-Liesa, et al.Cell|June 17, 1994
Dihydropyridine receptor mutations cause hypokalemic periodic paralysisL J Ptácek, R Tawil, R C Griggs, et al.The Journal of General Physiology|August 30, 2000
Fundamental gating mechanism of nicotinic receptor channel revealed by mutation causing a congenital myasthenic syndromeH L Wang, K Ohno, M Milone, et al.Neuron|April 16, 1998
Mode switching kinetics produced by a naturally occurring mutation in the cytoplasmic loop of the human acetylcholine receptor epsilon subunitM Milone, H L Wang, K Ohno, et al.Annals of Neurology|February 9, 2000
The spectrum of mutations causing end-plate acetylcholinesterase deficiencyK Ohno, A G Engel, J M Brengman, et al.Medicine|February 18, 1998
Retinocochleocerebral vasculopathyG W Petty, A G Engel, B R Younge, et al.Brain : a Journal of Neurology|June 1, 1993
Congenital endplate acetylcholinesterase deficiencyD O Hutchinson, T J Walls, S Nakano, et al.Human Molecular Genetics|September 1, 1996
New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndromeA G Engel, K Ohno, M Milone, et al.Human Molecular Genetics|May 1, 1997
Congenital myasthenic syndromes due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene: identification and functional characterization of six new mutationsK Ohno, P A Quiram, M Milone, et al.Pageof 22