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Andrew G Engel

Showing results (61-70 of 129) with videos related to

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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.
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.
Annals of the New York Academy of Sciences|June 24, 2008
Further observations in congenital myasthenic syndromesAndrew G Engel, Xin-Ming Shen, Duygu Selcen, et al.
Annals of Neurology|May 11, 2006
Slow-channel mutation in acetylcholine receptor alphaM4 domain and its efficient knockdownXin-Ming Shen, Feza Deymeer, Steven M Sine, et al.
Human Molecular Genetics|March 26, 2003
E-box mutations in the RAPSN promoter region in eight cases with congenital myasthenic syndromeKinji Ohno, Menachem Sadeh, Ilan Blatt, et al.
International Journal of Molecular Sciences|February 25, 2023
Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive ReviewKinji Ohno, Bisei Ohkawara, Xin-Ming Shen, et al.
Neuromuscular Disorders : NMD|March 14, 2020
A novel heterozygous mutation in the C-terminal region of HSPB8 leads to limb-girdle rimmed vacuolar myopathyStefan Nicolau, Teerin Liewluck, Jeffrey L Elliott, et al.
Journal of Clinical Neuromuscular Disease|April 28, 2012
Muscle restricted vasculitis causing dropped head syndrome: a case report and review of the literatureAmy Almaraz Nielsen, Benn E Smith, Andrew G Engel, et al.
Pageof 13

Showing results (61-70 of 129) with videos related to

Sort By:
Pageof 13
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.
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.
Annals of the New York Academy of Sciences|June 24, 2008
Further observations in congenital myasthenic syndromesAndrew G Engel, Xin-Ming Shen, Duygu Selcen, et al.
Annals of Neurology|May 11, 2006
Slow-channel mutation in acetylcholine receptor alphaM4 domain and its efficient knockdownXin-Ming Shen, Feza Deymeer, Steven M Sine, et al.
Human Molecular Genetics|March 26, 2003
E-box mutations in the RAPSN promoter region in eight cases with congenital myasthenic syndromeKinji Ohno, Menachem Sadeh, Ilan Blatt, et al.
International Journal of Molecular Sciences|February 25, 2023
Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive ReviewKinji Ohno, Bisei Ohkawara, Xin-Ming Shen, et al.
Neuromuscular Disorders : NMD|March 14, 2020
A novel heterozygous mutation in the C-terminal region of HSPB8 leads to limb-girdle rimmed vacuolar myopathyStefan Nicolau, Teerin Liewluck, Jeffrey L Elliott, et al.
Journal of Clinical Neuromuscular Disease|April 28, 2012
Muscle restricted vasculitis causing dropped head syndrome: a case report and review of the literatureAmy Almaraz Nielsen, Benn E Smith, Andrew G Engel, et al.
Pageof 13