Arylsulfatase K inactivation causes mucopolysaccharidosis due to deficient glucuronate desulfation of heparan and chondroitin sulfate

Brain Pathology in Mucopolysaccharidoses (MPS) Patients with Neurological Forms

(2020) Gustavo M. Viana et al.   Journal of Clinical Medicine

A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans

(2018) Samer Khateb et al.   GENETICS IN MEDICINE

A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease

(2016) Heike Wolf et al.   Disease Models & Mechanisms

Glycosaminoglycans and mucopolysaccharidosis type III

(2016) Grzegorz Wegrzyn   Frontiers in Bioscience-Landmark

The Anti-Osteoanabolic Function of Sclerostin Is Blunted in Mice Carrying a High Bone Mass Mutation of Lrp5

(2015) Timur A Yorgan et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Molecular Mechanism of Substrate Specificity for Heparan Sulfate 2-O-Sulfotransferase

(2014) Chunhui Liu et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Arylsulfatase K, a Novel Lysosomal Sulfatase

(2013) Elena Marie Wiegmann et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Glycan-based biomarkers for mucopolysaccharidoses

(2013) Roger Lawrence et al.   MOLECULAR GENETICS AND METABOLISM

Mucopolysaccharidoses

(2013) Rolando Cimaz et al.   Current Rheumatology Reports

Mass Spectrometric Method for Determining the Uronic Acid Epimerization in Heparan Sulfate Disaccharides Generated Using Nitrous Acid

(2012) Vanessa Leah Gill et al.   ANALYTICAL CHEMISTRY

Standardized nomenclature, symbols, and units for bone histomorphometry: A 2012 update of the report of the ASBMR Histomorphometry Nomenclature Committee

(2012) David W Dempster et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Iduronic Acid in Chondroitin/Dermatan Sulfate

(2012) Anders Malmström et al.   JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY

Disease-specific non–reducing end carbohydrate biomarkers for mucopolysaccharidoses

(2012) Roger Lawrence et al.   Nature Chemical Biology

Neuropathology in Mouse Models of Mucopolysaccharidosis Type I, IIIA and IIIB

(2012) Fiona L. Wilkinson et al.   PLoS One

Arylsulfatase G inactivation causes loss of heparan sulfate 3-O-sulfatase activity and mucopolysaccharidosis in mice

(2012) B. Kowalewski et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The cellular pathology of lysosomal diseases

(2011) Timothy M Cox et al.   JOURNAL OF PATHOLOGY

Target selection of heparan sulfate hexuronic acid 2-O-sulfotransferase

(2010) E. Smeds et al.   GLYCOBIOLOGY

Secondary Storage of Dermatan Sulfate in Sanfilippo Disease

(2010) William C. Lamanna et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Common and Uncommon Pathogenic Cascades in Lysosomal Storage Diseases

(2010) Einat B. Vitner et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Guidelines for assessment of bone microstructure in rodents using micro-computed tomography

(2010) Mary L Bouxsein et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Two Dermatan Sulfate Epimerases Form Iduronic Acid Domains in Dermatan Sulfate

(2009) Benny Pacheco et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Early signs of neurolipidosis-related behavioural alterations in a murine model of metachromatic leukodystrophy

(2008) Stijn Stroobants et al.   BEHAVIOURAL BRAIN RESEARCH

Proteomics of the lysosome

(2008) Torben Lübke et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

Evolutionary Differences in Glycosaminoglycan Fine Structure Detected by Quantitative Glycan Reductive Isotope Labeling

(2008) Roger Lawrence et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Quantitative determination of the glycosaminoglycan Δ-disaccharide composition of serum, platelets and granulocytes by reversed-phase high-performance liquid chromatography

(2008) Michael Ambrosius et al.   JOURNAL OF CHROMATOGRAPHY A

Disaccharide structure code for the easy representation of constituent oligosaccharides from glycosaminoglycans

(2008) Roger Lawrence et al.   NATURE METHODS