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Methods in Molecular Biology (Clifton, N.J.)|July 28, 2025
Restoration of Dysferlin After Exon 32 Skipping in Patient CellsFlorian Barthélémy, Sébastien Courrier, Marc Bartoli
Methods in Molecular Biology (Clifton, N.J.)|September 2, 2018
Dysferlin Exon 32 Skipping in Patient CellsFlorian Barthélémy, Sébastien Courrier, Nicolas Lévy, et al.
American Journal of Medical Genetics. Part A|September 7, 2006
ATRX syndrome in a girl with a heterozygous mutation in the ATRX Zn finger domain and a totally skewed X-inactivation patternCatherine Badens, Nathalie Martini, Sébastien Courrier, et al.
Frontiers in Cell and Developmental Biology|December 10, 2021
The Dysferlin Transcript Containing the Alternative Exon 40a is Essential for Myocyte FunctionsOcéane Ballouhey, Sébastien Courrier, Virginie Kergourlay, et al.
Applied & Translational Genomics|April 8, 2016
Comparing targeted exome and whole exome approaches for genetic diagnosis of neuromuscular disordersSvetlana Gorokhova, Mathieu Cerino, Yves Mathieu, et al.
Biomedicines|May 27, 2023
A Dysferlin Exon 32 Nonsense Mutant Mouse Model Shows Pathological Signs of DysferlinopathyOcéane Ballouhey, Marie Chapoton, Benedicte Alary, et al.
Cell Communication and Signaling : CCS|November 22, 2025
Zinc binding to a conserved motif in STIM1 induces clustering and SOCE activationBenedicte Alary, Viktoriia E Baksheeva, Sabrina Beaumier, et al.
The New Phytologist|February 22, 2005
Ectomycorrhizal symbiosis affects functional diversity of rhizosphere fluorescent pseudomonadsPascale Frey-Klett, Michaël Chavatte, Marie-Lise Clausse, et al.
Journal of Neuromuscular Diseases|November 19, 2016
Exon 32 Skipping of Dysferlin Rescues Membrane Repair in Patients' CellsFlorian Barthélémy, Cédric Blouin, Nicolas Wein, et al.
Human Molecular Genetics|July 5, 2011
High prevalence of laminopathies among patients with metabolic syndromeAnne Dutour, Patrice Roll, Bénédicte Gaborit, et al.
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