Gene expression during normal and FSHD myogenesis

The myogenic transcriptional network

(2011) Shigetoshi Yokoyama et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Retinal vascular disease and the pathogenesis of facioscapulohumeral muscular dystrophy. A signalling message from Wnt?

(2011) Robin B. Fitzsimons   NEUROMUSCULAR DISORDERS

Expression Profiling of FSHD-1 and FSHD-2 Cells during Myogenic Differentiation Evidences Common and Distinctive Gene Dysregulation Patterns

(2011) Stefania Cheli et al.   PLoS One

Comparative gene expression profiling between human cultured myotubes and skeletal muscle tissue

(2010) Frederic Raymond et al.   BMC GENOMICS

Transforming growth factor-β enhances matrix metalloproteinase-2 expression and activity through AKT in fibroblasts derived from angiofibromas in patients with tuberous sclerosis complex

(2010) C.-H. Lee et al.   BRITISH JOURNAL OF DERMATOLOGY

OASIS/CREB3L1 Induces Expression of Genes Involved in Extracellular Matrix Production But Not Classical Endoplasmic Reticulum Stress Response Genes in Pancreatic β-Cells

(2010) Ravi N. Vellanki et al.   ENDOCRINOLOGY

JunB transcription factor maintains skeletal muscle mass and promotes hypertrophy

(2010) Anna Raffaello et al.   JOURNAL OF CELL BIOLOGY

Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophy

(2010) Hongqing Du et al.   NATURE STRUCTURAL & MOLECULAR BIOLOGY

A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy

(2010) R. J. L. F. Lemmers et al.   SCIENCE

Facioscapulohumeral Dystrophy: Incomplete Suppression of a Retrotransposed Gene

(2010) Lauren Snider et al.   PLoS Genetics

Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level

(2009) Rinse Klooster et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy

(2009) Lauren Snider et al.   HUMAN MOLECULAR GENETICS

Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD

(2009) Jessica C. de Greef et al.   HUMAN MUTATION

Klhl31 is associated with skeletal myogenesis and its expression is regulated by myogenic signals and Myf-5

(2009) Alaa Abou-Elhamd et al.   MECHANISMS OF DEVELOPMENT

DNaseI hypersensitivity at gene-poor, FSH dystrophy-linked 4q35.2

(2009) Xueqing Xu et al.   NUCLEIC ACIDS RESEARCH

Embryonic vs. Adult Myogenesis: Challenging the 'Regeneration Recapitulates Development' Paradigm

(2009) J. Wang et al.   Journal of Molecular Cell Biology

Specific Loss of Histone H3 Lysine 9 Trimethylation and HP1γ/Cohesin Binding at D4Z4 Repeats Is Associated with Facioscapulohumeral Dystrophy (FSHD)

(2009) Weihua Zeng et al.   PLoS Genetics

An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies

(2008) Darko Bosnakovski et al.   EMBO JOURNAL

DUX4c, an FSHD candidate gene, interferes with myogenic regulators and abolishes myoblast differentiation

(2008) Darko Bosnakovski et al.   EXPERIMENTAL NEUROLOGY

Facioscapulohumeral muscular dystrophy

(2008) Rabi Tawil   Neurotherapeutics

Gene Expression Profiling in Limb-Girdle Muscular Dystrophy 2A

(2008) Amets Sáenz et al.   PLoS One