Dp412e: a novel human embryonic dystrophin isoform induced by BMP4 in early differentiated cells

The Pathogenesis and Therapy of Muscular Dystrophies

(2015) Simon Guiraud et al.   Annual Review of Genomics and Human Genetics

Abnormal splicing switch of DMD’s penultimate exon compromises muscle fibre maintenance in myotonic dystrophy

(2015) Frédérique Rau et al.   Nature Communications

Early pathogenesis of Duchenne muscular dystrophy modelled in patient-derived human induced pluripotent stem cells

(2015) Emi Shoji et al.   Scientific Reports

Dystrophin is a tumor suppressor in human cancers with myogenic programs

(2014) Yuexiang Wang et al.   NATURE GENETICS

Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice

(2014) Nicolas Wein et al.   NATURE MEDICINE

Duchenne and Becker Muscular Dystrophies

(2014) Kevin M. Flanigan   NEUROLOGIC CLINICS

Implication of Human Endogenous Retrovirus Envelope Proteins in Placental Functions

(2014) Adjimon Lokossou et al.   Viruses-Basel

Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophy

(2013) Alessandra Govoni et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Pharmacological prospects in the treatment of Duchenne muscular dystrophy

(2013) Urs T. Ruegg   CURRENT OPINION IN NEUROLOGY

Newborn bloodspot screening for Duchenne Muscular Dystrophy: 21 years experience in Wales (UK)

(2013) Stuart J Moat et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

DMD transcript imbalance determines dystrophin levels

(2013) Pietro Spitali et al.   FASEB JOURNAL

Paleovirology of 'syncytins', retroviral env genes exapted for a role in placentation

(2013) C. Lavialle et al.   PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES

Expression of Members of the Dystrophin, Dystrobrevin, and Dystrotelin Superfamily

(2012) Roland G. Roberts et al.   CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION

RNA Binding Protein/RNA Element Interactions and the Control of Translation

(2012) Xavier Pichon et al.   CURRENT PROTEIN & PEPTIDE SCIENCE

Genetic Therapeutic Approaches for Duchenne Muscular Dystrophy

(2012) Helen Foster et al.   HUMAN GENE THERAPY

Melanocytes-A novel tool to study mitochondrial dysfunction in Duchenne muscular dystrophy

(2012) Camilla Pellegrini et al.   JOURNAL OF CELLULAR PHYSIOLOGY

Gene and cell-mediated therapies for muscular dystrophy

(2012) Patryk Konieczny et al.   MUSCLE & NERVE

Primer3—new capabilities and interfaces

(2012) Andreas Untergasser et al.   NUCLEIC ACIDS RESEARCH

BRACHYURY and CDX2 Mediate BMP-Induced Differentiation of Human and Mouse Pluripotent Stem Cells into Embryonic and Extraembryonic Lineages

(2011) Andreia S. Bernardo et al.   Cell Stem Cell

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

(2011) Matteo Bovolenta et al.   HUMAN MUTATION

Protein Transfer Into Human Cells by VSV-G-induced Nanovesicles

(2011) Philippe-Emmanuel Mangeot et al.   MOLECULAR THERAPY

Muscle histology in fetuses at risk for Duchenne muscular dystrophy

(2010) James Toop et al.   CLINICAL GENETICS

Comparative analysis of antisense oligonucleotide sequences targeting exon 53 of the human DMD gene: Implications for future clinical trials

(2010) Linda J. Popplewell et al.   NEUROMUSCULAR DISORDERS

Muscular dystrophy begins early in embryonic development deriving from stem cell loss and disrupted skeletal muscle formation

(2009) D. Merrick et al.   Disease Models & Mechanisms

DMDexon 1 truncating point mutations: Amelioration of phenotype by alternative translation initiation in exon 6

(2009) Olga L. Gurvich 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

The impact of retrotransposons on human genome evolution

(2009) Richard Cordaux et al.   NATURE REVIEWS GENETICS

DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy

(2009) Kevin M. Flanigan et al.   NEUROMUSCULAR DISORDERS

Identification of Small Molecule and Genetic Modulators of AON-Induced Dystrophin Exon Skipping by High-Throughput Screening

(2009) Debra A. O'Leary et al.   PLoS One

Endogenous retroviruses

(2008) V. Blikstad et al.   CELLULAR AND MOLECULAR LIFE SCIENCES