Elisabeth Le Rumeur
Rennes, 35000, France
Last Updated: 09/26/2026
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Found 26 publications
How the central domain of dystrophin acts to bridge F-actin to sarcolemmal lipids.
Journal: Journal of structural biology
Published: June 03, 2019
Fine mapping of hydrophobic contacts reassesses the organization of the first three dystrophin coiled-coil repeats.
Journal: Protein science : a publication of the Protein Society
Published: July 09, 2018
Human Dystrophin Structural Changes upon Binding to Anionic Membrane Lipids.
Journal: Biophysical journal
Published: April 20, 2018
Sedentary lifestyle and urinary incontinence in women: A literature review
Journal: Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie
Published: February 20, 2018
Dystrophin's central domain forms a complex filament that becomes disorganized by in-frame deletions.
Journal: The Journal of biological chemistry
Published: August 02, 2017
Contrast-Matched Isotropic Bicelles: A Versatile Tool to Specifically Probe the Solution Structure of Peripheral Membrane Proteins Using SANS.
Journal: Langmuir : the ACS journal of surfaces and colloids
Published: June 06, 2017
Dystrophin and Spectrin, Two Highly Dissimilar Sisters of the Same Family.
Journal: Sub-cellular biochemistry
Published: January 20, 2017
Dystrophin Hot-Spot Mutants Leading to Becker Muscular Dystrophy Insert More Deeply into Membrane Models than the Native Protein.
Journal: Biochemistry
Published: July 02, 2016
IgA Structure Variations Associate with Immune Stimulations and IgA Mesangial Deposition.
Journal: Journal of the American Society of Nephrology : JASN
Published: August 18, 2015
Structural Basis of Neuronal Nitric-oxide Synthase Interaction with Dystrophin Repeats 16 and 17.
Journal: The Journal of biological chemistry
Published: July 24, 2015
Dystrophin and the two related genetic diseases, Duchenne and Becker muscular dystrophies.
Journal: Bosnian journal of basic medical sciences
Published: July 20, 2015
Abnormal splicing switch of DMD's penultimate exon compromises muscle fibre maintenance in myotonic dystrophy.
Journal: Nature communications
Published: January 30, 2015
Last Updated: 09/26/2026