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

Identification of a Post-translational Modification with Ribitol-Phosphate and Its Defect in Muscular Dystrophy

(2016) Motoi Kanagawa et al.   Cell Reports

Human ISPD Is a Cytidyltransferase Required for Dystroglycan O-Mannosylation

(2015) Moniek Riemersma et al.   CHEMISTRY & BIOLOGY

Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane

(2015) T. Yoshida-Moriguchi et al.   GLYCOBIOLOGY

Disease mutations in CMP-sialic acid transporter SLC35A1 result in abnormal  -dystroglycan O-mannosylation, independent from sialic acid

(2015) M. Riemersma et al.   HUMAN MOLECULAR GENETICS

Mammalian O-Mannosylation Pathway: Glycan Structures, Enzymes, and Protein Substrates

(2014) Jeremy L. Praissman et al.   BIOCHEMISTRY

Glycobiology of  -dystroglycan and muscular dystrophy

(2014) T. Endo   JOURNAL OF BIOCHEMISTRY

DAG1 mutations associated with asymptomatic hyperCKemia and hypoglycosylation of  -dystroglycan

(2014) M. Dong et al.   NEUROLOGY

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

In-Gel β-Elimination and Aqueous–Organic Partition for Improved O- and Sulfoglycomics

(2013) Tadahiro Kumagai et al.   ANALYTICAL CHEMISTRY

ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies

(2013) Sebahattin Cirak et al.   BRAIN

TheO-Mannosylation Pathway: Glycosyltransferases and Proteins Implicated in Congenital Muscular Dystrophy

(2013) Lance Wells   JOURNAL OF BIOLOGICAL CHEMISTRY

Enzymatic Basis forN-Glycan Sialylation

(2013) Lu Meng et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Homozygous dystroglycan mutation associated with a novel muscle–eye–brain disease-like phenotype with multicystic leucodystrophy

(2013) Tobias Geis et al.   NEUROGENETICS

Mining the O-mannose glycoproteome reveals cadherins as major O-mannosylated glycoproteins

(2013) M. B. Vester-Christensen et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

SGK196 Is a Glycosylation-Specific O-Mannose Kinase Required for Dystroglycan Function

(2013) T. Yoshida-Moriguchi et al.   SCIENCE

Deciphering the Glycosylome of Dystroglycanopathies Using Haploid Screens for Lassa Virus Entry

(2013) L. T. Jae et al.   SCIENCE

Exome Sequencing and Functional Validation in Zebrafish Identify GTDC2 Mutations as a Cause of Walker-Warburg Syndrome

(2012) M. Chiara Manzini et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Identification of Mutations in TMEM5 and ISPD as a Cause of Severe Cobblestone Lissencephaly

(2012) Sandrine Vuillaumier-Barrot et al.   AMERICAN JOURNAL OF HUMAN GENETICS

NMR Characterization of Immunoglobulin G Fc Glycan Motion on Enzymatic Sialylation

(2012) Adam W. Barb et al.   BIOCHEMISTRY

O-Mannosylation and human disease

(2012) Christina M. Dobson et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Developmental Expression of the Neuron-specificN-Acetylglucosaminyltransferase Vb (GnT-Vb/IX) and Identification of Itsin VivoGlycan Products in Comparison with Those of Its Paralog, GnT-V

(2012) Jin Kyu Lee et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan

(2012) Tony Roscioli et al.   NATURE GENETICS

ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome

(2012) Tobias Willer et al.   NATURE GENETICS

SIFT web server: predicting effects of amino acid substitutions on proteins

(2012) Ngak-Leng Sim et al.   NUCLEIC ACIDS RESEARCH

Muscular dystrophies due to glycosylation defects

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

Mammalian O-mannosylation: unsolved questions of structure/function

(2011) Stephanie H Stalnaker et al.   CURRENT OPINION IN STRUCTURAL BIOLOGY

Cell-matrix interactions in muscle disease

(2011) Virginie Carmignac et al.   JOURNAL OF PATHOLOGY

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

Oxidative stress, inflammation and carcinogenesis are controlled through the pentose phosphate pathway by transaldolase

(2011) Andras Perl et al.   TRENDS IN MOLECULAR MEDICINE

Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing

(2010) Hane Lee et al.   BMC GENOMICS

Site Mapping and Characterization ofO-Glycan Structures on α-Dystroglycan Isolated from Rabbit Skeletal Muscle

(2010) Stephanie H. Stalnaker et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

A minimal peptide substrate in biotin holoenzyme synthetase-catalyzed biotinylation

(2010) Dorothy Beckett et al.   PROTEIN SCIENCE

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

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

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

Phenotypic and Genetic Analysis of a Large Family With Migraine-Associated Vertigo

(2008) Hane Lee et al.   HEADACHE

Synthesis of CDP-Activated Ribitol for Teichoic Acid Precursors in Streptococcus pneumoniae

(2008) S. Baur et al.   JOURNAL OF BACTERIOLOGY