Dystrophin Hot-Spot Mutants Leading to Becker Muscular Dystrophy Insert More Deeply into Membrane Models than the Native Protein
Author:
Affiliation:
1. Université de Rennes 1, 35042 Rennes, France
2. UMR CNRS 6251, Institut de Physique de Rennes, 35042 Rennes, France
3. UMR CNRS 6290, Équipe SIM, 35043 Rennes, France
Funder
AFM-Téléthon
Ministère de l'Enseignement Supérieur et de la Recherche
Conseil Régional de Bretagne
European Regional Development Fund
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.biochem.6b00290
Reference38 articles.
1. Isolated dystrophin molecules as seen by electron microscopy.
2. Pathophysiology of Duchenne Muscular Dystrophy: Current Hypotheses
3. Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials
4. Dystrophin levels and clinical severity in Becker muscular dystrophy patients
5. Dystrophin as a therapeutic biomarker: Are we ignoring data from the past?
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1. A label-free approach for measuring interactions of proteins with lipid membranes;Cell Reports Methods;2023-11
2. Genotype–phenotype correlation in Becker muscular dystrophy in Chinese patients;Journal of Human Genetics;2018-07-05
3. Préclinique : La dystrophine présente plusieurs sites indépendants pour son ancrage membranaire;médecine/sciences;2016-11
4. Gene Editing for Duchenne Muscular Dystrophy Using the CRISPR/Cas9 Technology: The Importance of Fine-tuning the Approach;Molecular Therapy;2016-11
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