Abnormal Skeletal Muscle Regeneration plus Mild Alterations in Mature Fiber Type Specification in Fktn-Deficient Dystroglycanopathy Muscular Dystrophy Mice

POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations

(2014) Stefania Di Costanzo et al.   HUMAN MOLECULAR GENETICS

Dystroglycan Binding to α-Neurexin Competes with Neurexophilin-1 and Neuroligin in the Brain

(2014) Carsten Reissner et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Development of Rabbit Monoclonal Antibodies for Detection of Alpha-Dystroglycan in Normal and Dystrophic Tissue

(2014) Marisa J. Fortunato et al.   PLoS One

Contribution of Dysferlin Deficiency to Skeletal Muscle Pathology in Asymptomatic and Severe Dystroglycanopathy Models: Generation of a New Model for Fukuyama Congenital Muscular Dystrophy

(2014) Motoi Kanagawa et al.   PLoS One

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

(2013) Valentina Sancisi et al.   AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY

Dystrophin complex functions as a scaffold for signalling proteins

(2013) Bruno Constantin   BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES

Dissecting the Molecular Basis of the Role of the O-Mannosylation Pathway in Disease: α-Dystroglycan and Forms of Muscular Dystrophy

(2013) David Live et al.   CHEMBIOCHEM

Impaired viability of muscle precursor cells in muscular dystrophy with glycosylation defects and amelioration of its severe phenotype by limited gene expression

(2013) Motoi Kanagawa et al.   HUMAN MOLECULAR GENETICS

LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy

(2013) Matthew M. Goddeeris et al.   NATURE

Characteristics of magnetic resonance imaging biomarkers in a natural history study of golden retriever muscular dystrophy

(2013) Zheng Fan et al.   NEUROMUSCULAR DISORDERS

Mouse fukutin deletion impairs dystroglycan processing and recapitulates muscular dystrophy

(2012) Aaron M. Beedle et al.   JOURNAL OF CLINICAL INVESTIGATION

Fatigue in muscular dystrophies

(2012) Corrado Angelini et al.   NEUROMUSCULAR DISORDERS

Sarcolemma instability during mechanical activity in Large myd cardiac myocytes with loss of dystroglycan extracellular matrix receptor function

(2011) Zhyldyz Kabaeva et al.   HUMAN MOLECULAR GENETICS

Chronic AMPK activation evokes the slow, oxidative myogenic program and triggers beneficial adaptations in mdx mouse skeletal muscle

(2011) V. Ljubicic et al.   HUMAN MOLECULAR GENETICS

Fiber Types in Mammalian Skeletal Muscles

(2011) Stefano Schiaffino et al.   PHYSIOLOGICAL REVIEWS

Soleus muscle in glycosylation-deficient muscular dystrophy is protected from contraction-induced injury

(2010) Jessica D. Gumerson et al.   AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY

Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres

(2010) Capucine Trollet et al.   HUMAN MOLECULAR GENETICS

Posttetanic potentiation in mdx muscle

(2010) Ian Curtis Smith et al.   JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY

Type 2 Myotonic Dystrophy Can Be Predicted by the Combination of Type 2 Muscle Fiber Central Nucleation and Scattered Atrophy

(2009) Guillaume Bassez et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Basal lamina strengthens cell membrane integrity via the laminin G domain-binding motif of  -dystroglycan

(2009) R. Han et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA