Structural Basis of Neuronal Nitric-oxide Synthase Interaction with Dystrophin Repeats 16 and 17

Genetics and Emerging Treatments for Duchenne and Becker Muscular Dystrophy

(2015) Nicolas Wein et al.   PEDIATRIC CLINICS OF NORTH AMERICA

Innovative interactive flexible docking method for multi-scale reconstruction elucidates dystrophin molecular assembly

(2014) A.-E. Molza et al.   FARADAY DISCUSSIONS

Becker muscular dystrophy severity is linked to the structure of dystrophin

(2014) Aurélie Nicolas et al.   HUMAN MOLECULAR GENETICS

Molecular architecture of mammalian nitric oxide synthases

(2014) M. G. Campbell et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Molecular Clues about the Dystrophin–Neuronal Nitric Oxide Synthase Interaction: A Theoretical Approach

(2013) Emmanuel Giudice et al.   BIOCHEMISTRY

Therapy for Duchenne muscular dystrophy: renewed optimism from genetic approaches

(2013) Rebecca J. Fairclough et al.   NATURE REVIEWS GENETICS

Molecular dissection of dystrophin identifies the docking site for nNOS

(2013) S. Q. Harper   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Advances in X-ray scattering: from solution SAXS to achievements with coherent beams

(2012) Javier Pérez et al.   CURRENT OPINION IN STRUCTURAL BIOLOGY

Variable phenotype of del45-55 Becker patients correlated with nNOSµ mislocalization and RYR1 hypernitrosylation

(2012) Christel Gentil et al.   HUMAN MOLECULAR GENETICS

Nitric Oxide in Skeletal Muscle: Role on Mitochondrial Biogenesis and Function

(2012) Celia Tengan et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

New developments in theATSASprogram package for small-angle scattering data analysis

(2012) Maxim V. Petoukhov et al.   JOURNAL OF APPLIED CRYSTALLOGRAPHY

Assessment of the structural and functional impact of in-frame mutations of the DMD gene, using the tools included in the eDystrophin online database

(2012) Aurélie Nicolas et al.   Orphanet Journal of Rare Diseases

 2 and  3 helices of dystrophin R16 and R17 frame a microdomain in the  1 helix of dystrophin R17 for neuronal NOS binding

(2012) Y. Lai et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A graphical interface for the FoldX forcefield

(2011) J. Van Durme et al.   BIOINFORMATICS

Nitric oxide synthases: regulation and function

(2011) U. Forstermann et al.   EUROPEAN HEART JOURNAL

A biophysical map of the dystrophin rod

(2010) Ahmed Mirza et al.   BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS

Dystrophin: More than just the sum of its parts

(2010) Elisabeth Le Rumeur et al.   BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS

Crystal structure and functional interpretation of the erythrocyte spectrin tetramerization domain complex

(2010) J. J. Ipsaro et al.   BLOOD

PLATINUM: a web tool for analysis of hydrophobic/hydrophilic organization of biomolecular complexes

(2009) Timothy V. Pyrkov et al.   BIOINFORMATICS

Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort

(2009) Kevin M. Flanigan et al.   HUMAN MUTATION

Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase

(2009) Sylvie Tuffery-Giraud et al.   HUMAN MUTATION

Dystrophins carrying spectrin-like repeats 16 and 17 anchor nNOS to the sarcolemma and enhance exercise performance in a mouse model of muscular dystrophy

(2009) Yi Lai et al.   JOURNAL OF CLINICAL INVESTIGATION

Neuronal nitric oxide synthase: Structure, subcellular localization, regulation, and clinical implications

(2009) Li Zhou et al.   NITRIC OXIDE-BIOLOGY AND CHEMISTRY

I-TASSER: Fully automated protein structure prediction in CASP8

(2009) Yang Zhang   PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS