E. Young

Thematic review series: Lipid Posttranslational Modifications. Lysosomal metabolism of lipid-modified proteins

Function and Structure of a Prokaryotic Formylglycine-generating Enzyme

Complete Genetic Correction of iPS Cells From Duchenne Muscular Dystrophy

Ultrastructural Characterization of the Lower Motor System in a Mouse Model of Krabbe Disease

Bone marrow transplantation as effective treatment of central nervous system disease in globoid cell leukodystrophy, metachromatic leukodystrophy, adrenoleukodystrophy, mannosidosis, fucosidosis, aspartylglucosaminuria, Hurler, Maroteaux-Lamy, and Sly syndromes, and Gaucher disease type III

Targeted Disruption of the Cln3 Gene Provides a Mouse Model for Batten Disease

A novel role for 12/15-lipoxygenase in regulating autophagy

Genetic medicines: treatment strategies for hereditary disorders

Lysosomal storage disorders

A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome)

Infiltrative Cardiovascular Diseases

Gene therapy for mucopolysaccharidosis

Recommendations for the Evaluation of Left Ventricular Diastolic Function by Echocardiography: An Update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging

Recommendations for the Evaluation of Left Ventricular Diastolic Function by Echocardiography: An Update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging

Mycobacterium tuberculosis Rv3406 Is a Type II Alkyl Sulfatase Capable of Sulfate Scavenging

Allogeneic bone marrow transplantation for lysosomal storage diseases

Molecular genetics of Krabbe disease (globoid cell leukodystrophy): Diagnostic and clinical implications

Protein therapeutics: a summary and pharmacological classification

Bioluminescent Probes of Sulfatase Activity

Lysosomal storage diseases

2021 Guideline for the Prevention of Stroke in Patients With Stroke and Transient Ischemic Attack: A Guideline From the American Heart Association/American Stroke Association

Mouse model for the lysosomal disorder galactosialidosis and correction of the phenotype with overexpressing erythroid precursor cells.

Enzyme replacement therapy for Anderson-Fabry disease

Beneficial roles of feed additives as immunostimulants in aquaculture: a review

Mitochondrial DNA and the origins of the domestic horse

Lysosomal cathepsin D mediates endogenous mucin glycodomain catabolism in mammals

Aggregation-Induced Emission: Together We Shine, United We Soar!

The Caenorhabditis elegans mucolipin-like gene cup-5 is essential for viability and regulates lysosomes in multiple cell types

SULFATASES AND HUMAN DISEASE

Click-Chemistry Based High Throughput Screening Platform for Modulators of Ras Palmitoylation

Zinc as an essential micronutrient: A review

Formylglycine, a Post-Translationally Generated Residue with Unique Catalytic Capabilities and Biotechnology Applications

Haemopoietic chimaerism: a complication in heterozygote detection tests for inherited defects in cattle

Isolated allogeneic bone marrow-derived mesenchymal cells engraft and stimulate growth in children with osteogenesis imperfecta: Implications for cell therapy of bone

Variability of acid hydrolase activities in cultured skin fibroblasts and amniotic fluid cells.

Is globotriaosylceramide a useful biomarker in Fabry disease?

A new simple enzyme assay for pre- and postnatal diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) and its variants

A 5' splice site mutation in fucosidosis.

The Acrodermatitis Enteropathica Mutation Transiently Affects Zinc Metabolism in Human Fibroblasts

Plasma chitotriosidase activity in Gaucher disease patients who have been treated either by bone marrow transplantation or by enzyme replacement therapy with alglucerase

Galactocerebrosidase Deficiency in Globoid Cell Leucodystrophy of Late Onset

Bone marrow transplantation for Maroteaux–Lamy syndrome (MPS VI): Long‐term follow‐up

Allogeneic bone marrow transplantation for fucosidosis.

Long‐term follow‐up following bone marrow transplantation for Hunter disease

Bone marrow transplantation for Sanfilippo disease type B