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G Engel

Showing results (401-410 of 741) with videos related to

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Human Molecular Genetics|September 23, 2008
hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndromeAkio Masuda, Xin-Ming Shen, Mikako Ito, et al.
Neurology|February 17, 2017
Congenital myopathy associated with the triadin knockout syndromeAndrew G Engel, Keeley R Redhage, David J Tester, et al.
Muscle & Nerve|December 1, 1993
Congenital myasthenic syndromes: I. Deficiency and short open-time of the acetylcholine receptorA G Engel, A Nagel, T J Walls, et al.
Neuromuscular Disorders : NMD|August 6, 2019
A homozygous mutation in GMPPB leads to centronuclear myopathy with combined pre- and postsynaptic defects of neuromuscular transmissionStefan Nicolau, Teerin Liewluck, Xin-Ming Shen, et al.
Surgery for Obesity and Related Diseases : Official Journal of the American Society for Bariatric Surgery|November 28, 2022
Deficits in cognitive control during alcohol consumption after bariatric surgeryGail A Kerver, Scott G Engel, John Gunstad, et al.
Surgery for Obesity and Related Diseases : Official Journal of the American Society for Bariatric Surgery|March 20, 2013
Blood alcohol concentrations rise rapidly and dramatically after Roux-en-Y gastric bypassKristine J Steffen, Scott G Engel, Garrett A Pollert, et al.
Brain : a Journal of Neurology|June 1, 1989
Inclusion body myositis. Observations in 40 patientsB P Lotz, A G Engel, H Nishino, et al.
Journal of Palliative Medicine|October 20, 2023
Emergency Palliative Care: Early Assessment of an Older Adult With a Fall and Hip FractureMaura Kennedy, Janet S Rico, Shan W Liu, et al.
American Journal of Human Genetics|August 12, 1999
Congenital end-plate acetylcholinesterase deficiency caused by a nonsense mutation and an A-->G splice-donor-site mutation at position +3 of the collagenlike-tail-subunit gene (COLQ): how does G at position +3 result in aberrant splicing?K Ohno, J M Brengman, K J Felice, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|September 1, 1983
Evidence for common pharmacological properties of [3H]5-hydroxytryptamine binding sites, presynaptic 5-hydroxytryptamine autoreceptors in CNS and inhibitory presynaptic 5-hydroxytryptamine receptors on sympathetic nervesG Engel, M Göthert, E Müller-Schweinitzer, et al.
Pageof 75

Showing results (401-410 of 741) with videos related to

Sort By:
Pageof 75
Human Molecular Genetics|September 23, 2008
hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndromeAkio Masuda, Xin-Ming Shen, Mikako Ito, et al.
Neurology|February 17, 2017
Congenital myopathy associated with the triadin knockout syndromeAndrew G Engel, Keeley R Redhage, David J Tester, et al.
Muscle & Nerve|December 1, 1993
Congenital myasthenic syndromes: I. Deficiency and short open-time of the acetylcholine receptorA G Engel, A Nagel, T J Walls, et al.
Neuromuscular Disorders : NMD|August 6, 2019
A homozygous mutation in GMPPB leads to centronuclear myopathy with combined pre- and postsynaptic defects of neuromuscular transmissionStefan Nicolau, Teerin Liewluck, Xin-Ming Shen, et al.
Surgery for Obesity and Related Diseases : Official Journal of the American Society for Bariatric Surgery|November 28, 2022
Deficits in cognitive control during alcohol consumption after bariatric surgeryGail A Kerver, Scott G Engel, John Gunstad, et al.
Surgery for Obesity and Related Diseases : Official Journal of the American Society for Bariatric Surgery|March 20, 2013
Blood alcohol concentrations rise rapidly and dramatically after Roux-en-Y gastric bypassKristine J Steffen, Scott G Engel, Garrett A Pollert, et al.
Brain : a Journal of Neurology|June 1, 1989
Inclusion body myositis. Observations in 40 patientsB P Lotz, A G Engel, H Nishino, et al.
Journal of Palliative Medicine|October 20, 2023
Emergency Palliative Care: Early Assessment of an Older Adult With a Fall and Hip FractureMaura Kennedy, Janet S Rico, Shan W Liu, et al.
American Journal of Human Genetics|August 12, 1999
Congenital end-plate acetylcholinesterase deficiency caused by a nonsense mutation and an A-->G splice-donor-site mutation at position +3 of the collagenlike-tail-subunit gene (COLQ): how does G at position +3 result in aberrant splicing?K Ohno, J M Brengman, K J Felice, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|September 1, 1983
Evidence for common pharmacological properties of [3H]5-hydroxytryptamine binding sites, presynaptic 5-hydroxytryptamine autoreceptors in CNS and inhibitory presynaptic 5-hydroxytryptamine receptors on sympathetic nervesG Engel, M Göthert, E Müller-Schweinitzer, et al.
Pageof 75