| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1992PNAS...89.2561R |
| P356 | DOI | 10.1073/PNAS.89.7.2561 |
| P953 | full work available at URL | https://europepmc.org/articles/PMC48701 |
| https://europepmc.org/articles/PMC48701?pdf=render | ||
| P932 | PMC publication ID | 48701 |
| P698 | PubMed publication ID | 1348358 |
| P5875 | ResearchGate publication ID | 21808068 |
| P2093 | author name string | K. von Figura | |
| von Figura K | |||
| W. Rommerskirch | |||
| P2860 | cites work | Phylogenetic conservation of arylsulfatases. cDNA cloning and expression of human arylsulfatase B | Q24300265 |
| Cloning and expression of human arylsulfatase A | Q24316271 | ||
| Cloning and expression of human steroid-sulfatase. Membrane topology, glycosylation, and subcellular distribution in BHK-21 cells | Q24339110 | ||
| Arylsulfatase A pseudodeficiency: loss of a polyadenylylation signal and N-glycosylation site | Q24601866 | ||
| Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease | Q26778460 | ||
| Molecular basis of different forms of metachromatic leukodystrophy | Q28240698 | ||
| Structure of the arylsulfatase A gene | Q28258513 | ||
| Genetic complementation studies of multiple sulfatase deficiency | Q33989276 | ||
| Complementation of multiple sulfatase deficiency in somatic cell hybrids | Q35199889 | ||
| Presence of arylsulfatase A (ARS A) in multiple sulfatase deficiency disorder fibroblasts | Q35202748 | ||
| Arysulfatase A modulation with pH in multiple sulfatase deficiency disorder fibroblasts | Q35203477 | ||
| Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts | Q36412160 | ||
| Redesign of retrovirus packaging cell lines to avoid recombination leading to helper virus production | Q36918698 | ||
| Juvenile and adult metachromatic leukodystrophy: partial restoration of arylsulfatase A (cerebroside sulfatase) activity by inhibitors of thiol proteinases | Q37690419 | ||
| A universal retroviral vector for efficient constitutive expression of exogenous genes | Q40390282 | ||
| Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency. | Q41483368 | ||
| Restoration of arylsulphatase A activity in human-metachromatic-leucodystrophy fibroblasts via retroviral-vector-mediated gene transfer | Q41655421 | ||
| Restoration of arylsulphatase B activity in human mucopolysaccharidosis-type-VI fibroblasts by retroviral-vector-mediated gene transfer | Q41681536 | ||
| Purification and properties of arylsulfatase. A from human urine | Q44812061 | ||
| Biosynthesis and maturation of arylsulfatase B in normal and mutant cultured human fibroblasts. | Q54486137 | ||
| Synthesis and stability of steroid sulfatase in fibroblasts from multiple sulfatase deficiency | Q67923556 | ||
| Structural and immunochemical characterization of human urine arylsulfatase A purified by affinity chromatography | Q69856203 | ||
| Synthesis and stability of arylsulfatase A and B in fibroblasts from multiple sulfatase deficiency | Q69868272 | ||
| Steroid sulfatase. Biosynthesis and processing in normal and mutant fibroblasts | Q70007084 | ||
| Rapid degradation of steroid sulfatase in multiple sulfatase deficiency | Q70283014 | ||
| Enhanced breakdown of arylsulfatase A in multiple sulfatase deficiency | Q72525562 | ||
| Synthesis and Processing of Arylsulfatase A in Human Skin Fibroblasts | Q72525731 | ||
| The assay of arylsulphatases A and B in human urine | Q78694080 | ||
| P433 | issue | 7 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 5 | |
| P304 | page(s) | 2561-2565 | |
| P577 | publication date | 1992-04-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Multiple sulfatase deficiency: catalytically inactive sulfatases are expressed from retrovirally introduced sulfatase cDNAs | |
| P478 | volume | 89 |
| Q74512006 | COS cell expression studies of P86L, P86R, P480L and P480Q Hunter's disease-causing mutations |
| Q41093667 | Characterization of iduronate sulphatase mutants affecting N-glycosylation sites and the cysteine-84 residue |
| Q41059465 | Conversion of cysteine to formylglycine in eukaryotic sulfatases occurs by a common mechanism in the endoplasmic reticulum |
| Q36631537 | Conversion of cysteine to formylglycine: a protein modification in the endoplasmic reticulum |
| Q28568685 | Ethanol decreases rat hepatic arylsulfatase A activity levels |
| Q61041512 | Expression of five iduronate-2-sulfatase site-directed mutations |
| Q34393884 | Expression, localization, structural, and functional characterization of pFGE, the paralog of the Calpha-formylglycine-generating enzyme |
| Q54446678 | First evidences for a third sulfatase maturation system in prokaryotes from E. coli aslB and ydeM deletion mutants. |
| Q38290367 | Formylglycine, a post-translationally generated residue with unique catalytic capabilities and biotechnology applications. |
| Q38296444 | Heparan N-sulfatase: cysteine 70 plays a role in the enzyme catalysis and processing |
| Q41093678 | Immortalization and characterization of a cell line exhibiting a severe multiple sulphatase deficiency phenotype |
| Q28646260 | Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme |
| Q42137916 | Overexpression of N-acetylgalactosamine-4-sulphatase induces a multiple sulphatase deficiency in mucopolysaccharidosis-type-VI fibroblasts |
| Q40549709 | Overexpression of inactive arylsulphatase mutants and in vitro activation by light-dependent oxidation with vanadate |
| Q37781746 | Pathology and Current Treatment of Neurodegenerative Sphingolipidoses |
| Q37102138 | Rapid degradation of an active formylglycine generating enzyme variant leads to a late infantile severe form of multiple sulfatase deficiency. |
| Q42701927 | SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiency |
| Q40008271 | The non-catalytic N-terminal extension of formylglycine-generating enzyme is required for its biological activity and retention in the endoplasmic reticulum |
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