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Research article

First published 2011-11

Unmasking Potential Intracellular Roles For Dysferlin through Improved Immunolabeling Methods

Joseph A. Roche, Lisa W. Ru, Andrea M. O’Neill [...]

Journal of Histochemistry & Cytochemistry

Free access

Research article

First published

Exon 32 Skipping of Dysferlin Rescues Membrane Repair in Patients’ Cells

Florian Barthélémy, Cédric Blouin, Nicolas Wein [...]

Journal of Neuromuscular Diseases

Retricted access

Research article

First published 2020-04

Antisense-Mediated Skipping of Dysferlin Exons in Control and Dysferlinopathy Patient-Derived Cells

Nisha Verwey, Isabella Gazzoli, Sabine Krause [...]

Nucleic Acid Therapeutics

Retricted access

Research article

First published 2013-11

Bone Marrow Transplantation in Dysferlin-Deficient Mice Results in a Mild Functional Improvement

Bàrbara Flix, Xavier Suárez-Calvet, Jordi Díaz-Manera [...]

Stem Cells and Development

Retricted access

Research article

First published 2013-06

The Phenotype of Dysferlin-Deficient Mice Is Not Rescued by Adeno-Associated Virus–Mediated Transfer of Anoctamin 5

François Monjaret, Laurence Suel-Petat, Nathalie Bourg-Alibert [...]

Human Gene Therapy Clinical Development

Open access

Review article

First published 2018-2-21

Muscle Cells Fix Breaches by Orchestrating a Membrane Repair Ballet

Florian Barthélémy, Aurélia Defour, Nicolas Lévy [...]

Journal of Neuromuscular Diseases

Open access

Research article

First published 2018-07

Systemic Delivery of Dysferlin Overlap Vectors Provides Long-Term Gene Expression and Functional Improvement for Dysferlinopathy

Rachael A. Potter, Danielle A. Griffin, Patricia C. Sondergaard [...]

Human Gene Therapy

Retricted access

Research article

First published

Dysferlin Homozygous Mutation G1418D Causes Limb-Girdle Type 2B in a Mexican Family

H. Rosas-Vargas, B. Gómez-Díaz, L. Ruano-Calderón [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Letter

First published 2010-02

Exclusion of Mutations in the Dysferlin Alternative Exons 1 of DYSF-v1,5a,and 40a in a Cohort of 26 Patients

Martin Krahn, Véronique Labelle, Ana Borges [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Research article

First published 2009-08

Identification of Different Genomic Deletions and One Duplication in the Dysferlin Gene Using Multiplex Ligation-Dependent Probe Amplification and Genomic Quantitative PCR

Martin Krahn, Ana Borges, Claire Navarro [...]

Genetic Testing and Molecular Biomarkers

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