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Current Opinion in Cardiology|March 16, 2018
Genetic basis of arrhythmogenic cardiomyopathyJennifer Karmouch, Alexandros Protonotarios, Petros Syrris
Chemico-Biological Interactions|October 24, 2012
Developmental consequences of the ColQ/MuSK interactionsJennifer Karmouch, Alexandre Dobbertin, Severine Sigoillot, et al.
Molecular and Cellular Biology|January 23, 2009
Antiapoptotic role for ornithine decarboxylase during oocyte maturationYong Zhou, Chunqi Ma, Jennifer Karmouch, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 20, 2016
Neuromuscular junction immaturity and muscle atrophy are hallmarks of the ColQ-deficient mouse, a model of congenital myasthenic syndrome with acetylcholinesterase deficiencySéverine M Sigoillot, Francine Bourgeois, Jennifer Karmouch, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 7, 2015
HuR Mediates Changes in the Stability of AChR β-Subunit mRNAs after Skeletal Muscle DenervationOlivier R Joassard, Guy Bélanger, Jennifer Karmouch, et al.
Frontiers in Molecular Neuroscience|December 28, 2020
AChR β-Subunit mRNAs Are Stabilized by HuR in a Mouse Model of Congenital Myasthenic Syndrome With Acetylcholinesterase DeficiencyJennifer Karmouch, Perrine Delers, Fannie Semprez, et al.
Development (Cambridge, England)|November 26, 2008
SIT1 is a betaine/proline transporter that is activated in mouse eggs after fertilization and functions until the 2-cell stageMohamed-Kheir Idris Anas, Martin B Lee, Chenxi Zhou, et al.
Cardiovascular Research|July 28, 2019
Exercise restores dysregulated gene expression in a mouse model of arrhythmogenic cardiomyopathySirisha M Cheedipudi, Jinzhu Hu, Siyang Fan, et al.
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