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CELL, ISSN 0092-8674, 05/2003, Volume 113, Issue 4, pp. 435 - 444
C-alpha-formylglycine (FGly) is the catalytic residue in the active site of eukaryotic sulfatases. It is posttranslationally generated from a cysteine in the... 
POSTTRANSLATIONAL FORMATION | HUMAN ARYLSULFATASE-A | EUKARYOTIC SULFATASES | MECHANISM | CONVERSION | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROTEIN MODIFICATION | CYSTEINE | ENDOPLASMIC-RETICULUM | FIBROBLASTS | CELL BIOLOGY | Enzymes | Cell research | Composition | Gene mutations | Analysis | Physiological aspects | Genetic aspects | Minerals in nutrition | Gene expression | Glycine
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 11/2018, Volume 33, Issue 13, pp. 820 - 824
Multiple sulfatase deficiency is an autosomal recessive lysosomal storage disorder due to a deficiency in formylglycine-generating enzyme, which is encoded by... 
sulfatases | Austin disease | multiple sulfatase deficiency | mucosulfatidosis | lysosomal storage disorders | SUMF1 | SUMF1 MUTATIONS | PEDIATRICS | CLINICAL NEUROLOGY
Journal Article
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 06/2016, Volume 101, Issue 6, pp. 2545 - 2553
Journal Article
Human Gene Therapy, ISSN 1043-0342, 08/2017, Volume 28, Issue 8, pp. 626 - 638
Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare X-linked recessive lysosomal disorder caused by defective iduronate-2-sulfatase (IDS),... 
Research Articles | Hunter syndrome | gene therapy | neurocognitive function | mucopolysaccharidosis type II | AAV | MEDICINE, RESEARCH & EXPERIMENTAL | HURLER-SYNDROME | STORAGE DISEASE | BONE-MARROW-TRANSPLANTATION | CNS | DELIVERY | MURINE MODEL | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | MOUSE MODEL | GENETICS & HEREDITY | BLOOD-BRAIN | ENZYME REPLACEMENT THERAPY | EXPRESSION | Dependovirus - genetics | Genetic Therapy | Central Nervous System - metabolism | Genetic Vectors - administration & dosage | Iduronate Sulfatase - metabolism | Humans | Male | Cognition | Tissue Distribution | Time Factors | Mucopolysaccharidosis II - therapy | Mucopolysaccharidosis II - genetics | Female | Gene Order | Disease Models, Animal | Gene Transfer Techniques | Gene Expression | Iduronate Sulfatase - blood | Transduction, Genetic | Glycosaminoglycans - metabolism | Genetic Vectors - genetics | Neuropsychological Tests | Mucopolysaccharidosis II - blood | Pilot Projects | Animals | Iduronate Sulfatase - genetics | Mice | Enzyme Activation | Mucopolysaccharidosis II - psychology | Heparan sulfate | Brain | Animal models | Glycosaminoglycans | Gene transfer | Central nervous system | Organs | Disorders | Viruses | Nervous system | Mucopolysaccharidosis | Injection | Sulfates | Tissues | Hereditary diseases | Prevention | Gag protein | Sulfate | Circulation | Index Medicus
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 03/2018, Volume 123, Issue 3, pp. 337 - 346
Journal Article
Cell, ISSN 0092-8674, 2003, Volume 113, Issue 4, pp. 445 - 456
In multiple sulfatase deficiency (MSD), a human inherited disorder, the activities of all sulfatases are impaired due to a defect in posttranslational... 
Journal Article
Journal Article