Altered Tnnt3 characterizes selective weakness of fast fibers in mice overexpressing FSHD region gene 1 (FRG1)

Large scale genotype–phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy

(2013) Giulia Ricci et al.   BRAIN

Overexpression of facioscapulohumeral muscular dystrophy region gene 1 causes primary defects in myogenic stem cells

(2013) A. Xynos et al.   JOURNAL OF CELL SCIENCE

Sarcomeric dysfunction contributes to muscle weakness in facioscapulohumeral muscular dystrophy

(2013) S. Lassche et al.   NEUROLOGY

Rbfox1 Downregulation and Altered Calpain 3 Splicing by FRG1 in a Mouse Model of Facioscapulohumeral Muscular Dystrophy (FSHD)

(2013) Mariaelena Pistoni et al.   PLoS Genetics

Intrinsic Epigenetic Regulation of the D4Z4 Macrosatellite Repeat in a Transgenic Mouse Model for FSHD

(2013) Yvonne D. Krom et al.   PLoS Genetics

Large-Scale Population Analysis Challenges the Current Criteria for the Molecular Diagnosis of Fascioscapulohumeral Muscular Dystrophy

(2012) Isabella Scionti et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Expression of DUX4 in zebrafish development recapitulates facioscapulohumeral muscular dystrophy

(2012) Hiroaki Mitsuhashi et al.   HUMAN MOLECULAR GENETICS

FSHD: copy number variations on the theme of muscular dystrophy

(2010) Daphne Selvaggia Cabianca et al.   JOURNAL OF CELL BIOLOGY

Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites

(2010) Q. Liu et al.   JOURNAL OF CELL SCIENCE

A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score

(2010) Costanza Lamperti et al.   MUSCLE & NERVE

A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy

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

Therapy for neuromuscular disorders

(2009) Andrea LH Arnett et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Measurement of the Functional Status of Patients with Different Types of Muscular Dystrophy

(2009) Yi-Jing Lue et al.   KAOHSIUNG JOURNAL OF MEDICAL SCIENCES

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

Mechanisms of Muscle Degeneration, Regeneration, and Repair in the Muscular Dystrophies

(2008) Gregory Q. Wallace et al.   Annual Review of Physiology

Muscular dystrophy candidate gene FRG1 is critical for muscle development

(2008) Meredith L. Hanel et al.   DEVELOPMENTAL DYNAMICS

High-frequency fatigue of skeletal muscle: role of extracellular Ca2+

(2008) Elena Germinario et al.   EUROPEAN JOURNAL OF APPLIED PHYSIOLOGY

Structural Basis for the Regulation of Muscle Contraction by Troponin and Tropomyosin

(2008) Agnieszka Galińska-Rakoczy et al.   JOURNAL OF MOLECULAR BIOLOGY

Different types of fatigue in patients with facioscapulohumeral dystrophy, myotonic dystrophy and HMSN-I. Experienced fatigue and physiological fatigue

(2008) Joke S. Kalkman et al.   NEUROLOGICAL SCIENCES

Hand weakness in Duchenne muscular dystrophy and its relation to physical disability

(2008) Fabiana Luisa Mattar et al.   NEUROMUSCULAR DISORDERS