Human N-acetylgalactosamine-4-sulphate sulphatase. Purification, monoclonal antibody production and native and subunit Mr values.
about
Immunopurification and characterization of human alpha-L-iduronidase with the use of monoclonal antibodiesHuman liver iduronate-2-sulphatase. Purification, characterization and catalytic propertiesHuman liver N-acetylgalactosamine 6-sulphatase. Purification and characterizationA cDNA clone for human glucosamine-6-sulphatase reveals differences between arylsulphatases and non-arylsulphatasesReview: the immunochemical analysis of enzyme from mucopolysaccharidoses patients.Mucopolysaccharidosis VI.Mucopolysaccharidosis type VI: Structural and clinical implications of mutations in N-acetylgalactosamine-4-sulfatase.Mucopolysaccharidosis type VI: identification of three mutations in the arylsulfatase B gene of patients with the severe and mild phenotypes provides molecular evidence for genetic heterogeneity.Analysis of N-acetylgalactosamine-4-sulfatase protein and kinetics in mucopolysaccharidosis type VI patientsIdentification, expression, and biochemical characterization of N-acetylgalactosamine-4-sulfatase mutations and relationship with clinical phenotype in MPS-VI patientsSulfatases: structure, mechanism, biological activity, inhibition, and synthetic utility.Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndrome.Sulfatase activities towards the regulation of cell metabolism and signaling in mammals.Processing of normal lysosomal and mutant N-acetylgalactosamine 4-sulphatase: BiP (immunoglobulin heavy-chain binding protein) may interact with critical protein contact sites.Lysosomal enzyme replacement therapies: Historical development, clinical outcomes, and future perspectives.Mutational analysis of mucopolysaccharidosis type VI patients undergoing a trial of enzyme replacement therapy.Conversion of cysteine to formylglycine in eukaryotic sulfatases occurs by a common mechanism in the endoplasmic reticulum.Immortalization and characterization of a cell line exhibiting a severe multiple sulphatase deficiency phenotype.Correction of human mucopolysaccharidosis type-VI fibroblasts with recombinant N-acetylgalactosamine-4-sulphatase.Human N-acetylgalactosamine-4-sulphatase biosynthesis and maturation in normal, Maroteaux-Lamy and multiple-sulphatase-deficient fibroblasts.A specific fluorogenic assay for N-acetylgalactosamine-4-sulphatase activity using immunoadsorption.Human liver glucuronate 2-sulphatase. Purification, characterization and catalytic propertiesalpha-L-iduronidase in normal and mucopolysaccharidosis-type-I human skin fibroblasts.Overexpression of N-acetylgalactosamine-4-sulphatase induces a multiple sulphatase deficiency in mucopolysaccharidosis-type-VI fibroblasts.Mutational analysis of 105 mucopolysaccharidosis type VI patients.Arylsulfatase B Mediates the Sulfonation-Transport Interplay in Human Embryonic Kidney 293 Cells Overexpressing Sulfotransferase 1A3.Mild feline mucopolysaccharidosis type VI. Identification of an N-acetylgalactosamine-4-sulfatase mutation causing instability and increased specific activity.
P2860
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P2860
Human N-acetylgalactosamine-4-sulphate sulphatase. Purification, monoclonal antibody production and native and subunit Mr values.
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
1987年论文
@zh
1987年论文
@zh-cn
name
Human N-acetylgalactosamine-4- ...... native and subunit Mr values.
@en
Human N-acetylgalactosamine-4- ...... native and subunit Mr values.
@nl
type
label
Human N-acetylgalactosamine-4- ...... native and subunit Mr values.
@en
Human N-acetylgalactosamine-4- ...... native and subunit Mr values.
@nl
prefLabel
Human N-acetylgalactosamine-4- ...... native and subunit Mr values.
@en
Human N-acetylgalactosamine-4- ...... native and subunit Mr values.
@nl
P2093
P2860
P356
P1433
P1476
Human N-acetylgalactosamine-4- ...... native and subunit Mr values.
@en
P2093
Clements PR
Hopwood JJ
Saccone GT
P2860
P304
P356
10.1042/BJ2480755
P407
P577
1987-12-01T00:00:00Z