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European Heart Journal
|
December 25, 2016
Optogenetic termination of ventricular arrhythmias in the whole heart: towards biological cardiac rhythm management
Emile C A Nyns, Annemarie Kip, Cindy I Bart, et al.
Brain Structure & Function
|
April 19, 2014
Tomosyn-2 is required for normal motor performance in mice and sustains neurotransmission at motor endplates
Cornelia J Geerts, Jaap J Plomp, Bastijn Koopmans, et al.
Brain Research
|
February 27, 2007
Redundancy of Cav2.1 channel accessory subunits in transmitter release at the mouse neuromuscular junction
Simon Kaja, Boyan Todorov, Rob C G van de Ven, et al.
Brain : a Journal of Neurology
|
January 11, 2008
Eculizumab prevents anti-ganglioside antibody-mediated neuropathy in a murine model
Susan K Halstead, Femke M P Zitman, Peter D Humphreys, et al.
Journal of Neurophysiology
|
July 16, 2010
Severe and progressive neurotransmitter release aberrations in familial hemiplegic migraine type 1 Cacna1a S218L knock-in mice
Simon Kaja, Rob C G Van de Ven, Ludo A M Broos, et al.
Plos One
|
August 21, 2019
Cross-sectional study into age-related pathology of mouse models for limb girdle muscular dystrophy types 2D and 2F
Ingrid E C Verhaart, Kayleigh Putker, Davy van de Vijver, et al.
Autoimmunity Reviews
|
March 29, 2013
Pathophysiology of myasthenia gravis with antibodies to the acetylcholine receptor, muscle-specific kinase and low-density lipoprotein receptor-related protein 4
Jan J G M Verschuuren, Maartje G Huijbers, Jaap J Plomp, et al.
Neuromuscular Disorders : NMD
|
November 9, 2025
Antisense-mediated exon skipping therapy improves neuromuscular junction deficits in a Duchenne muscular dystrophy mouse model
Elizabeth M van der Pijl, Svetlana Pasteuning-Vuhman, Johanna Boertje-van der Meulen, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 18, 2005
Overexpression of GD1a ganglioside sensitizes motor nerve terminals to anti-GD1a antibody-mediated injury in a model of acute motor axonal neuropathy
John A Goodfellow, Tyrone Bowes, Kazim Sheikh, et al.
Journal of Neuromuscular Diseases
|
October 12, 2020
Simvastatin Treatment Does Not Ameliorate Muscle Pathophysiology in a Mouse Model for Duchenne Muscular Dystrophy
Ingrid E C Verhaart, Ornella Cappellari, Christa L Tanganyika-de Winter, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 68) with videos related to
Sort By:
Page
of 7
European Heart Journal
|
December 25, 2016
Optogenetic termination of ventricular arrhythmias in the whole heart: towards biological cardiac rhythm management
Emile C A Nyns, Annemarie Kip, Cindy I Bart, et al.
Brain Structure & Function
|
April 19, 2014
Tomosyn-2 is required for normal motor performance in mice and sustains neurotransmission at motor endplates
Cornelia J Geerts, Jaap J Plomp, Bastijn Koopmans, et al.
Brain Research
|
February 27, 2007
Redundancy of Cav2.1 channel accessory subunits in transmitter release at the mouse neuromuscular junction
Simon Kaja, Boyan Todorov, Rob C G van de Ven, et al.
Brain : a Journal of Neurology
|
January 11, 2008
Eculizumab prevents anti-ganglioside antibody-mediated neuropathy in a murine model
Susan K Halstead, Femke M P Zitman, Peter D Humphreys, et al.
Journal of Neurophysiology
|
July 16, 2010
Severe and progressive neurotransmitter release aberrations in familial hemiplegic migraine type 1 Cacna1a S218L knock-in mice
Simon Kaja, Rob C G Van de Ven, Ludo A M Broos, et al.
Plos One
|
August 21, 2019
Cross-sectional study into age-related pathology of mouse models for limb girdle muscular dystrophy types 2D and 2F
Ingrid E C Verhaart, Kayleigh Putker, Davy van de Vijver, et al.
Autoimmunity Reviews
|
March 29, 2013
Pathophysiology of myasthenia gravis with antibodies to the acetylcholine receptor, muscle-specific kinase and low-density lipoprotein receptor-related protein 4
Jan J G M Verschuuren, Maartje G Huijbers, Jaap J Plomp, et al.
Neuromuscular Disorders : NMD
|
November 9, 2025
Antisense-mediated exon skipping therapy improves neuromuscular junction deficits in a Duchenne muscular dystrophy mouse model
Elizabeth M van der Pijl, Svetlana Pasteuning-Vuhman, Johanna Boertje-van der Meulen, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 18, 2005
Overexpression of GD1a ganglioside sensitizes motor nerve terminals to anti-GD1a antibody-mediated injury in a model of acute motor axonal neuropathy
John A Goodfellow, Tyrone Bowes, Kazim Sheikh, et al.
Journal of Neuromuscular Diseases
|
October 12, 2020
Simvastatin Treatment Does Not Ameliorate Muscle Pathophysiology in a Mouse Model for Duchenne Muscular Dystrophy
Ingrid E C Verhaart, Ornella Cappellari, Christa L Tanganyika-de Winter, et al.
Page
of 7