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Human Mutation|October 15, 2014
Identification of splicing defects caused by mutations in the dysferlin geneVirginie Kergourlay, Ghadi Raï, Gaëlle Blandin, et al.
Scientific Reports|April 12, 2020
A new tool CovReport generates easy-to-understand sequencing coverage summary for diagnostic reportsMark Gorokhov, Mathieu Cerino, Jérémie Mortreux, et al.
Analytical Biochemistry|June 11, 2002
Quantification of splice variants using molecular beacon or scorpion primersMathieu Taveau, Daniel Stockholm, Melissa Spencer, et al.
Expert Review of Cardiovascular Therapy|November 27, 2007
Efficacy and safety of fondaparinux in patients with acute coronary syndromesJean-Pierre Bassand, Isabelle Richard-Lordereau, Yves Cadroy
Learning & Behavior|April 24, 2023
Context-induced renewal of passive but not active coping behaviours in the shock-probe defensive burying taskAlexa Brown, Melissa Martins, Isabelle Richard, et al.
Biochimica Et Biophysica Acta. Proteins and Proteomics|February 5, 2021
Calpains for dummies: What you need to know about the calpain familySimone Spinozzi, Sonia Albini, Heather Best, et al.
Physiotherapy Theory and Practice|March 10, 2018
Factors influencing physiotherapists' attitudes and beliefs toward chronic low back pain: Impact of a care network belongingAudrey Petit, Cyril Begue, Isabelle Richard, et al.
European Journal of Translational Myology|September 17, 2021
A revised model for mitochondrial dysfunction in Duchenne muscular dystrophyAi Vu Hong, Mathilde Sanson, Isabelle Richard, et al.
Human Mutation|July 4, 2019
Functional and cellular localization diversity associated with Fukutin-related protein patient genetic variantsSara F Henriques, Evelyne Gicquel, Justine Marsolier, et al.
Neurobiology of Disease|December 16, 2016
A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndromeValerie Matagne, Yann Ehinger, Lydia Saidi, et al.
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