Differentiation-related glycan epitopes identify discrete domains of the muscle glycocalyx

The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition

(2016) Jeremy L Praissman et al.   eLife

Helicobacter pylori chronic infection and mucosal inflammation switches the human gastric glycosylation pathways

(2015) Ana Magalhães et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

Galectin-1 Protein Therapy Prevents Pathology and Improves Muscle Function in the mdx Mouse Model of Duchenne Muscular Dystrophy

(2015) Pam M Van Ry et al.   MOLECULAR THERAPY

Mechanisms Regulating Neuromuscular Junction Development and Function and Causes of Muscle Wasting

(2015) Lionel A. Tintignac et al.   PHYSIOLOGICAL REVIEWS

Changes in glycosaminoglycan structure on differentiation of human embryonic stem cells towards mesoderm and endoderm lineages

(2014) Leyla Gasimli et al.   BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS

Glycobiology of  -dystroglycan and muscular dystrophy

(2014) T. Endo   JOURNAL OF BIOCHEMISTRY

The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated α-dystroglycan functional glycosylation

(2014) Tobias Willer et al.   eLife

B4GAT1 is the priming enzyme for the LARGE-dependent functional glycosylation of α-dystroglycan

(2014) Jeremy L Praissman et al.   eLife

Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan

(2013) Elizabeth Stevens et al.   AMERICAN JOURNAL OF HUMAN GENETICS

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

B3GALNT2 is a gene associated with congenital muscular dystrophy with brain malformations

(2013) Carola Hedberg et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

N-Glycolylneuraminic acid deficiency worsens cardiac and skeletal muscle pathophysiology in α-sarcoglycan-deficient mice

(2013) Paul T Martin et al.   GLYCOBIOLOGY

High Throughput Screening for Compounds That Alter Muscle Cell Glycosylation Identifies New Role forN-Glycans in Regulating Sarcolemmal Protein Abundance and Laminin Binding

(2012) Paula V. Cabrera et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Sarcospan-dependent Akt activation is required for utrophin expression and muscle regeneration

(2012) Jamie L. Marshall et al.   JOURNAL OF CELL BIOLOGY

Decreased surface sialic acid content is a sensitive indicator of muscle damage

(2012) Yuko Iwata et al.   MUSCLE & NERVE

Differential glycosylation of  -dystroglycan and proteins other than  -dystroglycan by like-glycosyltransferase

(2011) P. Zhang et al.   GLYCOBIOLOGY

Biglycan recruits utrophin to the sarcolemma and counters dystrophic pathology in mdx mice

(2010) A. R. Amenta et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

O-Mannosyl Phosphorylation of Alpha-Dystroglycan Is Required for Laminin Binding

(2010) T. Yoshida-Moriguchi et al.   SCIENCE

A Human-Specific Deletion in Mouse Cmah Increases Disease Severity in the mdx Model of Duchenne Muscular Dystrophy

(2010) K. Chandrasekharan et al.   Science Translational Medicine

The Mouse C2C12 Myoblast Cell SurfaceN-Linked Glycoproteome

(2009) Rebekah L. Gundry et al.   MOLECULAR & CELLULAR PROTEOMICS

Regulation of Glycan Structures in Animal Tissues

(2008) Alison V. Nairn et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Focused glycomic analysis of the N-linked glycan biosynthetic pathway in ovarian cancer

(2008) Karen L. Abbott et al.   PROTEOMICS