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G Engel

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Proceedings of the National Academy of Sciences of the United States of America|February 1, 1982
Acetylcholinesterase of human erythrocytes and neuromuscular junctions: homologies revealed by monoclonal antibodiesD M Fambrough, A G Engel, T L Rosenberry
Neurology|August 1, 1972
Progressive ataxia, retinal degeneration, neuromyopathy, and mental subnormality in a patient with true hypoparathyroidism, dwarfism, malabsorption, and cholelithiasisM R Gomez, A G Engel, P J Dyck
Annals of Neurology|April 1, 1977
A new myasthenic syndrome with end-plate acetylcholinesterase deficiency, small nerve terminals, and reduced acetylcholine releaseA G Engel, E H Lambert, M R Gomez
Annals of the New York Academy of Sciences|January 1, 1976
Experimental acetylcholine blockade of the neuromuscular junction. Effects on end plate and muscle fiber ultrastructureS S Freeman, A G Engel, D B Drachman
Naunyn-Schmiedeberg'S Archives of Pharmacology|September 1, 1989
Characterization of an endothelial 5-hydroxytryptamine (5-HT) receptor mediating relaxation of the porcine coronary arteryG J Molderings, G Engel, E Roth, et al.
The Journal of Experimental Medicine|December 1, 1992
Autoaggressive myocytotoxic T lymphocytes expressing an unusual gamma/delta T cell receptorG Pluschke, D Rüegg, R Hohlfeld, et al.
Archives Internationales De Pharmacodynamie Et De Therapie|September 1, 1992
Spiperone-induced endothelium-dependent relaxation of porcine coronary artery: an investigation into the underlying mechanismG J Molderings, G Engel, E Roth, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 5, 1998
Human endplate acetylcholinesterase deficiency caused by mutations in the collagen-like tail subunit (ColQ) of the asymmetric enzymeK Ohno, J Brengman, A Tsujino, et al.
Mayo Clinic Proceedings|October 1, 1971
Multicore disease. A recently recognized congenital myopathy associated with multifocal degeneration of muscle fibersA G Engel, M R Gomez, R V Groover
Anesthesia and Analgesia|May 1, 1997
Malignant hyperthermia testing in patients with persistently increased serum creatine kinase levelsM R Weglinski, D J Wedel, A G Engel
Pageof 75

Showing results (251-260 of 741) with videos related to

Sort By:
Pageof 75
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1982
Acetylcholinesterase of human erythrocytes and neuromuscular junctions: homologies revealed by monoclonal antibodiesD M Fambrough, A G Engel, T L Rosenberry
Neurology|August 1, 1972
Progressive ataxia, retinal degeneration, neuromyopathy, and mental subnormality in a patient with true hypoparathyroidism, dwarfism, malabsorption, and cholelithiasisM R Gomez, A G Engel, P J Dyck
Annals of Neurology|April 1, 1977
A new myasthenic syndrome with end-plate acetylcholinesterase deficiency, small nerve terminals, and reduced acetylcholine releaseA G Engel, E H Lambert, M R Gomez
Annals of the New York Academy of Sciences|January 1, 1976
Experimental acetylcholine blockade of the neuromuscular junction. Effects on end plate and muscle fiber ultrastructureS S Freeman, A G Engel, D B Drachman
Naunyn-Schmiedeberg'S Archives of Pharmacology|September 1, 1989
Characterization of an endothelial 5-hydroxytryptamine (5-HT) receptor mediating relaxation of the porcine coronary arteryG J Molderings, G Engel, E Roth, et al.
The Journal of Experimental Medicine|December 1, 1992
Autoaggressive myocytotoxic T lymphocytes expressing an unusual gamma/delta T cell receptorG Pluschke, D Rüegg, R Hohlfeld, et al.
Archives Internationales De Pharmacodynamie Et De Therapie|September 1, 1992
Spiperone-induced endothelium-dependent relaxation of porcine coronary artery: an investigation into the underlying mechanismG J Molderings, G Engel, E Roth, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 5, 1998
Human endplate acetylcholinesterase deficiency caused by mutations in the collagen-like tail subunit (ColQ) of the asymmetric enzymeK Ohno, J Brengman, A Tsujino, et al.
Mayo Clinic Proceedings|October 1, 1971
Multicore disease. A recently recognized congenital myopathy associated with multifocal degeneration of muscle fibersA G Engel, M R Gomez, R V Groover
Anesthesia and Analgesia|May 1, 1997
Malignant hyperthermia testing in patients with persistently increased serum creatine kinase levelsM R Weglinski, D J Wedel, A G Engel
Pageof 75