Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A G Engel

Showing results (231-240 of 242) with videos related to

Pageof 25
Sort By:
Neurology|February 28, 2002
Three novel COLQ mutations and variation of phenotypic expressivity due to G240XY A Shapira, M E Sadeh, M P Bergtraum, et al.
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.
Pageof 25

Showing results (231-240 of 242) with videos related to

Sort By:
Pageof 25
Neurology|February 28, 2002
Three novel COLQ mutations and variation of phenotypic expressivity due to G240XY A Shapira, M E Sadeh, M P Bergtraum, et al.
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.
Pageof 25