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Andrew G Engel

Showing results (111-120 of 129) with videos related to

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Scientific Reports|August 19, 2015
SRSF1 and hnRNP H antagonistically regulate splicing of COLQ exon 16 in a congenital myasthenic syndromeMohammad Alinoor Rahman, Yoshiteru Azuma, Farhana Nasrin, et al.
Neuromuscular Disorders : NMD|October 7, 2018
Corrigendum to "Congenital myasthenic syndromes in Turkey: Clinical clues and prognosis with long term follow-up" [Neuromuscular Disorders 28/4 (2018) 315-322]Hacer Durmus, Xin-Ming Shen, Piraye Serdaroglu-Oflazer, et al.
Annals of Clinical and Translational Neurology|February 8, 2017
Novel synaptobrevin-1 mutation causes fatal congenital myasthenic syndromeXin-Ming Shen, Rosana H Scola, Paulo J Lorenzoni, et al.
Scientific Reports|September 11, 2015
Collagen Q and anti-MuSK autoantibody competitively suppress agrin/LRP4/MuSK signalingKenji Otsuka, Mikako Ito, Bisei Ohkawara, et al.
Human Molecular Genetics|November 16, 2013
LRP4 third β-propeller domain mutations cause novel congenital myasthenia by compromising agrin-mediated MuSK signaling in a position-specific mannerBisei Ohkawara, Macarena Cabrera-Serrano, Tomohiko Nakata, et al.
Neurology|June 6, 2008
Translating research into treatmentsJohn H Noseworthy, Robert A Gross, Andrew G Engel, et al.
European Journal of Pharmacology|May 22, 2002
Effects of ginsenosides, active components of ginseng, on nicotinic acetylcholine receptors expressed in Xenopus oocytesSeok Choi, Se Yeon Jung, Jun Ho Lee, et al.
The Journal of General Physiology|October 3, 2002
Naturally occurring mutations at the acetylcholine receptor binding site independently alter ACh binding and channel gatingSteven M Sine, Xing-Ming Shen, Hai-Long Wang, et al.
JCI Insight|April 10, 2020
Congenital myasthenic syndrome-associated agrin variants affect clustering of acetylcholine receptors in a domain-specific mannerBisei Ohkawara, XinMing Shen, Duygu Selcen, et al.
JCI Insight|January 26, 2018
Mutations causing congenital myasthenia reveal principal coupling pathway in the acetylcholine receptor ε-subunitXin-Ming Shen, Joan M Brengman, Shelley Shen, et al.
Pageof 13

Showing results (111-120 of 129) with videos related to

Sort By:
Pageof 13
Scientific Reports|August 19, 2015
SRSF1 and hnRNP H antagonistically regulate splicing of COLQ exon 16 in a congenital myasthenic syndromeMohammad Alinoor Rahman, Yoshiteru Azuma, Farhana Nasrin, et al.
Neuromuscular Disorders : NMD|October 7, 2018
Corrigendum to "Congenital myasthenic syndromes in Turkey: Clinical clues and prognosis with long term follow-up" [Neuromuscular Disorders 28/4 (2018) 315-322]Hacer Durmus, Xin-Ming Shen, Piraye Serdaroglu-Oflazer, et al.
Annals of Clinical and Translational Neurology|February 8, 2017
Novel synaptobrevin-1 mutation causes fatal congenital myasthenic syndromeXin-Ming Shen, Rosana H Scola, Paulo J Lorenzoni, et al.
Scientific Reports|September 11, 2015
Collagen Q and anti-MuSK autoantibody competitively suppress agrin/LRP4/MuSK signalingKenji Otsuka, Mikako Ito, Bisei Ohkawara, et al.
Human Molecular Genetics|November 16, 2013
LRP4 third β-propeller domain mutations cause novel congenital myasthenia by compromising agrin-mediated MuSK signaling in a position-specific mannerBisei Ohkawara, Macarena Cabrera-Serrano, Tomohiko Nakata, et al.
Neurology|June 6, 2008
Translating research into treatmentsJohn H Noseworthy, Robert A Gross, Andrew G Engel, et al.
European Journal of Pharmacology|May 22, 2002
Effects of ginsenosides, active components of ginseng, on nicotinic acetylcholine receptors expressed in Xenopus oocytesSeok Choi, Se Yeon Jung, Jun Ho Lee, et al.
The Journal of General Physiology|October 3, 2002
Naturally occurring mutations at the acetylcholine receptor binding site independently alter ACh binding and channel gatingSteven M Sine, Xing-Ming Shen, Hai-Long Wang, et al.
JCI Insight|April 10, 2020
Congenital myasthenic syndrome-associated agrin variants affect clustering of acetylcholine receptors in a domain-specific mannerBisei Ohkawara, XinMing Shen, Duygu Selcen, et al.
JCI Insight|January 26, 2018
Mutations causing congenital myasthenia reveal principal coupling pathway in the acetylcholine receptor ε-subunitXin-Ming Shen, Joan M Brengman, Shelley Shen, et al.
Pageof 13