Rapid, comprehensive analysis of the dystrophin transcript by a custom micro-fluidic exome array

Current Status of Pharmaceutical and Genetic Therapeutic Approaches to Treat DMD

(2011) Christophe Pichavant et al.   MOLECULAR THERAPY

Systemic Administration of PRO051 in Duchenne's Muscular Dystrophy

(2011) Nathalie M. Goemans et al.   NEW ENGLAND JOURNAL OF MEDICINE

Reliable resequencing of the human dystrophin locus by universal long polymerase chain reaction and massive pyrosequencing

(2010) Raoul Jean Pierre Bonnal et al.   ANALYTICAL BIOCHEMISTRY

Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene

(2010) Kevin M. Flanigan et al.   HUMAN MUTATION

Dystrophin Isoform Induction In Vivo by Antisense-mediated Alternative Splicing

(2010) Sue Fletcher et al.   MOLECULAR THERAPY

Best Practice Guidelines on molecular diagnostics in Duchenne/Becker muscular dystrophies

(2010) Stephen Abbs et al.   NEUROMUSCULAR DISORDERS

Prenatal diagnosis of Duchenne muscular dystrophy by comparative genomic hybridization

(2009) M Bovolenta et al.   CLINICAL GENETICS

Dystrophin restoration in skeletal, heart and skin arrector pili smooth muscle of mdx mice by ZM2 NP–AON complexes

(2009) A Ferlini et al.   GENE THERAPY

Immortalized Skin Fibroblasts Expressing Conditional MyoD as a Renewable and Reliable Source of Converted Human Muscle Cells to Assess Therapeutic Strategies for Muscular Dystrophies: Validation of an Exon-Skipping Approach to Restore Dystrophin in Duchenne Muscular Dystrophy Cells

(2009) Soraya Chaouch et al.   HUMAN GENE THERAPY

Exon skipping-mediated dystrophin reading frame restoration for small mutations

(2009) Pietro Spitali et al.   HUMAN MUTATION

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

Local restoration of dystrophin expression with the morpholino oligomer AVI-4658 in Duchenne muscular dystrophy: a single-blind, placebo-controlled, dose-escalation, proof-of-concept study

(2009) Maria Kinali et al.   LANCET NEUROLOGY

A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies

(2008) Matteo Bovolenta et al.   BMC GENOMICS

Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization

(2008) Daniela del Gaudio et al.   HUMAN MUTATION

Microarray-based mutation detection in thedystrophingene

(2008) Madhuri R. Hegde et al.   HUMAN MUTATION

Integrated DNA, cDNA, and protein studies in Becker muscular dystrophy show high exception to the reading frame rule

(2008) Akanchha Kesari et al.   HUMAN MUTATION

Transcriptional behavior of DMD gene duplications in DMD/BMD males

(2008) F. Gualandi et al.   HUMAN MUTATION