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Andrew G Engel

Showing results (91-100 of 129) with videos related to

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Neurology|September 10, 2020
Determinants of the repetitive-CMAP occurrence and therapy efficacy in slow-channel myastheniaLi Di, Hai Chen, Yan Lu, et al.
Annals of the New York Academy of Sciences|June 24, 2008
Recent structural and mechanistic insights into endplate acetylcholine receptorsSteven M Sine, Fan Gao, Won Yong Lee, et al.
The EMBO Journal|May 8, 2004
Choline acetyltransferase structure reveals distribution of mutations that cause motor disordersYiying Cai, Ciarán N Cronin, Andrew G Engel, et al.
Annals of Neurology|December 17, 2008
Mutation in BAG3 causes severe dominant childhood muscular dystrophyDuygu Selcen, Francesco Muntoni, Barbara K Burton, et al.
Annals of the New York Academy of Sciences|November 1, 2003
Mechanistic diversity underlying fast channel congenital myasthenic syndromesSteven M Sine, Hai-Long Wang, Kinji Ohno, et al.
Neurology|April 25, 2014
DPAGT1 myasthenia and myopathy: genetic, phenotypic, and expression studiesDuygu Selcen, Xin-Ming Shen, Joan Brengman, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 3, 2006
Reconstitution of paired T cell receptor alpha- and beta-chains from microdissected single cells of human inflammatory tissuesSabine Seitz, Christian K Schneider, Joachim Malotka, et al.
Neurology|March 11, 2014
PREPL deficiency with or without cystinuria causes a novel myasthenic syndromeLuc Régal, Xin-Ming Shen, Duygu Selcen, et al.
The Journal of Clinical Investigation|February 18, 2003
Mutation causing severe myasthenia reveals functional asymmetry of AChR signature cystine loops in agonist binding and gatingXin-Ming Shen, Kinji Ohno, Akira Tsujino, et al.
Annals of Clinical and Translational Neurology|September 28, 2019
Slow-channel myasthenia due to novel mutation in M2 domain of AChR delta subunitXin-Ming Shen, Margherita Milone, Hang-Long Wang, et al.
Pageof 13

Showing results (91-100 of 129) with videos related to

Sort By:
Pageof 13
Neurology|September 10, 2020
Determinants of the repetitive-CMAP occurrence and therapy efficacy in slow-channel myastheniaLi Di, Hai Chen, Yan Lu, et al.
Annals of the New York Academy of Sciences|June 24, 2008
Recent structural and mechanistic insights into endplate acetylcholine receptorsSteven M Sine, Fan Gao, Won Yong Lee, et al.
The EMBO Journal|May 8, 2004
Choline acetyltransferase structure reveals distribution of mutations that cause motor disordersYiying Cai, Ciarán N Cronin, Andrew G Engel, et al.
Annals of Neurology|December 17, 2008
Mutation in BAG3 causes severe dominant childhood muscular dystrophyDuygu Selcen, Francesco Muntoni, Barbara K Burton, et al.
Annals of the New York Academy of Sciences|November 1, 2003
Mechanistic diversity underlying fast channel congenital myasthenic syndromesSteven M Sine, Hai-Long Wang, Kinji Ohno, et al.
Neurology|April 25, 2014
DPAGT1 myasthenia and myopathy: genetic, phenotypic, and expression studiesDuygu Selcen, Xin-Ming Shen, Joan Brengman, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 3, 2006
Reconstitution of paired T cell receptor alpha- and beta-chains from microdissected single cells of human inflammatory tissuesSabine Seitz, Christian K Schneider, Joachim Malotka, et al.
Neurology|March 11, 2014
PREPL deficiency with or without cystinuria causes a novel myasthenic syndromeLuc Régal, Xin-Ming Shen, Duygu Selcen, et al.
The Journal of Clinical Investigation|February 18, 2003
Mutation causing severe myasthenia reveals functional asymmetry of AChR signature cystine loops in agonist binding and gatingXin-Ming Shen, Kinji Ohno, Akira Tsujino, et al.
Annals of Clinical and Translational Neurology|September 28, 2019
Slow-channel myasthenia due to novel mutation in M2 domain of AChR delta subunitXin-Ming Shen, Margherita Milone, Hang-Long Wang, et al.
Pageof 13