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G Engel

Showing results (331-340 of 741) with videos related to

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Pediatric Neurology|July 5, 2012
Neuromuscular junction acetylcholinesterase deficiency responsive to albuterolSophelia H S Chan, Virginia C N Wong, Andrew G Engel
Neuromuscular Disorders : NMD|November 13, 2012
Scapuloperoneal muscular dystrophy phenotype due to TRIM32-sarcotubular myopathy in South Dakota HutteriteTeerin Liewluck, Jennifer A Tracy, Eric J Sorenson, et al.
Applied Optics|March 12, 2009
Modeling the absorption behavior of solar thermal collector coatings utilizing graded alpha-C:H/TiC layersD P Gruber, G Engel, H Sormann, et al.
The Journal of Physiology|March 11, 2006
The human adult subtype ACh receptor channel has high Ca2+ permeability and predisposes to endplate Ca2+ overloadingSergio Fucile, Antonietta Sucapane, Francesca Grassi, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|May 1, 1988
Characterisation of 5-HT3 recognition sites in membranes of NG 108-15 neuroblastoma-glioma cells with [3H]ICS 205-930H C Neijt, A Karpf, P Schoeffter, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|January 1, 1985
Lesioning of serotoninergic and noradrenergic nerve fibres of the rat brain does not decrease binding of 3H-clonidine and 3H-rauwolscine to cortical membranesG Gross, M Göthert, U Glapa, et al.
Annals of the New York Academy of Sciences|January 1, 1976
The motor end plate in myasthenia gravis and in experimental autoimmune myasthenia gravis. A quantitative ultrastructural studyA G Engel, M Tsujihata, J M Lindstrom, et al.
Neurology|November 19, 2011
Reducing bodies and myofibrillar myopathy features in FHL1 muscular dystrophyDuygu Selcen, Mark B Bromberg, Steven S Chin, et al.
Neuromuscular Disorders : NMD|March 24, 2004
Novel truncating RAPSN mutations causing congenital myasthenic syndrome responsive to 3,4-diaminopyridineBrenda L Banwell, Kinji Ohno, Joern P Sieb, et al.
Brain : a Journal of Neurology|December 24, 2004
Subunit-specific contribution to agonist binding and channel gating revealed by inherited mutation in muscle acetylcholine receptor M3-M4 linkerXin-Ming Shen, Kinji Ohno, Steven M Sine, et al.
Pageof 75

Showing results (331-340 of 741) with videos related to

Sort By:
Pageof 75
Pediatric Neurology|July 5, 2012
Neuromuscular junction acetylcholinesterase deficiency responsive to albuterolSophelia H S Chan, Virginia C N Wong, Andrew G Engel
Neuromuscular Disorders : NMD|November 13, 2012
Scapuloperoneal muscular dystrophy phenotype due to TRIM32-sarcotubular myopathy in South Dakota HutteriteTeerin Liewluck, Jennifer A Tracy, Eric J Sorenson, et al.
Applied Optics|March 12, 2009
Modeling the absorption behavior of solar thermal collector coatings utilizing graded alpha-C:H/TiC layersD P Gruber, G Engel, H Sormann, et al.
The Journal of Physiology|March 11, 2006
The human adult subtype ACh receptor channel has high Ca2+ permeability and predisposes to endplate Ca2+ overloadingSergio Fucile, Antonietta Sucapane, Francesca Grassi, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|May 1, 1988
Characterisation of 5-HT3 recognition sites in membranes of NG 108-15 neuroblastoma-glioma cells with [3H]ICS 205-930H C Neijt, A Karpf, P Schoeffter, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|January 1, 1985
Lesioning of serotoninergic and noradrenergic nerve fibres of the rat brain does not decrease binding of 3H-clonidine and 3H-rauwolscine to cortical membranesG Gross, M Göthert, U Glapa, et al.
Annals of the New York Academy of Sciences|January 1, 1976
The motor end plate in myasthenia gravis and in experimental autoimmune myasthenia gravis. A quantitative ultrastructural studyA G Engel, M Tsujihata, J M Lindstrom, et al.
Neurology|November 19, 2011
Reducing bodies and myofibrillar myopathy features in FHL1 muscular dystrophyDuygu Selcen, Mark B Bromberg, Steven S Chin, et al.
Neuromuscular Disorders : NMD|March 24, 2004
Novel truncating RAPSN mutations causing congenital myasthenic syndrome responsive to 3,4-diaminopyridineBrenda L Banwell, Kinji Ohno, Joern P Sieb, et al.
Brain : a Journal of Neurology|December 24, 2004
Subunit-specific contribution to agonist binding and channel gating revealed by inherited mutation in muscle acetylcholine receptor M3-M4 linkerXin-Ming Shen, Kinji Ohno, Steven M Sine, et al.
Pageof 75