Defects in Glycosylation Impair Satellite Stem Cell Function and Niche Composition in the Muscles of the Dystrophic LargemydMouse

Satellite cell senescence underlies myopathy in a mouse model of limb-girdle muscular dystrophy 2H

(2012) Elena Kudryashova et al.   JOURNAL OF CLINICAL INVESTIGATION

Dystroglycanopathies: coming into focus

(2011) Caroline Godfrey et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Muscular dystrophies due to glycosylation defects

(2011) Francesco Muntoni et al.   CURRENT OPINION IN NEUROLOGY

Satellite cells, connective tissue fibroblasts and their interactions are crucial for muscle regeneration

(2011) M. M. Murphy et al.   DEVELOPMENT

An absolute requirement for Pax7-positive satellite cells in acute injury-induced skeletal muscle regeneration

(2011) C. Lepper et al.   DEVELOPMENT

Ahnak1 abnormally localizes in muscular dystrophies and contributes to muscle vesicle release

(2011) Ute Zacharias et al.   JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY

Resveratrol Ameliorates Muscular Pathology in the Dystrophic mdx Mouse, a Model for Duchenne Muscular Dystrophy

(2011) Y. S. Hori et al.   JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS

A Dystroglycan Mutation Associated with Limb-Girdle Muscular Dystrophy

(2011) Yuji Hara et al.   NEW ENGLAND JOURNAL OF MEDICINE

Like-acetylglucosaminyltransferase (LARGE)-dependent modification of dystroglycan at Thr-317/319 is required for laminin binding and arenavirus infection

(2011) Y. Hara et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The muscle satellite cell at 50: the formative years

(2011) Juergen Scharner et al.   Skeletal Muscle

Sequential association of myogenic regulatory factors and E proteins at muscle-specific genes

(2011) Priya Londhe et al.   Skeletal Muscle

Short Telomeres and Stem Cell Exhaustion Model Duchenne Muscular Dystrophy in mdx/mTR Mice

(2010) Alessandra Sacco et al.   CELL

Elevated satellite cell number in Duchenne muscular dystrophy

(2010) Michael Kottlors et al.   CELL AND TISSUE RESEARCH

A transitional extracellular matrix instructs cell behavior during muscle regeneration

(2010) Sarah Calve et al.   DEVELOPMENTAL BIOLOGY

Deficiency of Dol-P-Man Synthase Subunit DPM3 Bridges the Congenital Disorders of Glycosylation with the Dystroglycanopathies

(2009) Dirk J. Lefeber et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Abnormal glycosylation of dystroglycan in human genetic disease

(2009) Jane E. Hewitt   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

Extracellular matrix components direct porcine muscle stem cell behavior

(2009) Karlijn J. Wilschut et al.   EXPERIMENTAL CELL RESEARCH

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

Mature Adult Dystrophic Mouse Muscle Environment Does Not Impede Efficient Engrafted Satellite Cell Regeneration and Self-Renewal

(2009) Luisa Boldrin et al.   STEM CELLS

Human Myoblast Engraftment Is Improved in Laminin-Enriched Microenvironment

(2009) Suse D. Silva-Barbosa et al.   TRANSPLANTATION

Laminin-111 Restores Regenerative Capacity in a Mouse Model for α7 Integrin Congenital Myopathy

(2008) Jachinta E. Rooney et al.   AMERICAN JOURNAL OF PATHOLOGY

Reduced proliferative activity of primary POMGnT1-null myoblasts in vitro

(2008) Yuko Miyagoe-Suzuki et al.   MECHANISMS OF DEVELOPMENT

The Muscle Stem Cell Niche: Regulation of Satellite Cells During Regeneration

(2008) Kristel J.M. Boonen et al.   TISSUE ENGINEERING PART B-REVIEWS

Severe muscle–eye–brain disease is associated with a homozygous mutation in the POMGnT1 gene

(2007) Serap Teber et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY