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Publications by Hugo Moser
SUMF1 Mutations Affecting Stability and Activity of Formylglycine Generating Enzyme Predict Clinical Outcome in Multiple Sulfatase Deficiency
European Journal of Human Genetics
Genetics
Genetic and Phenotypic Heterogeneity in Disorders of Peroxisome Biogenesis—A Complementation Study Involving Cell Lines From 19 Patients
Pediatric Research
Child Health
Pediatrics
Perinatology
Related publications
Structural Basis for Copper-Oxygen Mediated C−H Bond Activation by the Formylglycine-Generating Enzyme
Angewandte Chemie - International Edition
Catalysis
Chemistry
Sulfatase Modifying Factor 1 (SUMF1) Is Associated With Chronic Obstructive Pulmonary Disease
Respiratory Research
Pulmonary
Respiratory Medicine
Structural Basis for Copper-Oxygen Mediated C−H Bond Activation by the Formylglycine-Generating Enzyme
Angewandte Chemie
Structure of Formylglycine-Generating Enzyme in Complex With Copper and a Substrate Reveals an Acidic Pocket for Binding and Activation of Molecular Oxygen
Chemical Science
Chemistry
Cases With Toxicity of Anticholinesterase Enzyme and Factors Affecting Outcome
Journal of Pharmacology and Toxicology
Toxicology
Pharmaceutics
Pharmacology
The Defect in the Hunter Syndrome: Deficiency of Sulfoiduronate Sulfatase
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Reduced Antioxidant Enzyme Activity in Brains of Mice Transgenic for Human Presenilin-1 With Single or Multiple Mutations
Neuroscience Letters
Neuroscience
Leukocyte Adhesion Deficiency-Iii Is Caused by Mutations in KINDLIN3 Affecting Integrin Activation
Nature Medicine
Biochemistry
Medicine
Genetics
Molecular Biology
Evaluation of Pancreatin Stability Through Enzyme Activity Determination
Acta Pharmaceutica
Medicine
Pharmacology
Pharmaceutical Science
