about
Sanfilippo syndrome type C: deficiency of acetyl-CoA:alpha-glucosaminide N-acetyltransferase in skin fibroblastsMurine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiencyHigh performance liquid chromatographic strategy for the analysis of exopolysaccharides extracted from pathogenic bacteria.A new type of bacterial sulfatase reveals a novel maturation pathway in prokaryotes.Oxidative depolymerization of polysaccharides by reactive oxygen/nitrogen speciesArterial pathology in canine mucopolysaccharidosis-I and response to therapyGlycosaminoglycans in the human cornea: age-related changesMorphologic and biochemical studies of canine mucopolysaccharidosis I.The pathology of the feline model of mucopolysaccharidosis VI.Animal model of human disease: Mucopolysaccharidosis VI Maroteaux-Lamy syndrome, Arylsulfatase B-deficient mucopolysaccharidosis in the Siamese catCanine alpha-L-iduronidase deficiency. A model of mucopolysaccharidosis I.The pathology of the feline model of mucopolysaccharidosis ISuramin-induced storage disease. Mucopolysaccharidosis.Experimental animal model for mucopolysaccharidosis: suramin-induced glycosaminoglycan and sphingolipid accumulation in the rat.The synthesis of glycosaminoglycans by cultures of corneal stromal cells from patients with keratoconusSpondyloepiphyseal dysplasias and bilateral legg-calvé-perthes disease: diagnostic considerations for mucopolysaccharidosesPurine receptor antagonist modulates serology and affective behaviors in lupus-prone mice: evidence of autoimmune-induced pain?Liver-Directed Human Amniotic Epithelial Cell Transplantation Improves Systemic Disease Phenotype in Hurler Syndrome Mouse Model.Prenatal diagnosis of inborn errors of metabolism.Purification and properties of N-acetylgalactosamine 6-sulphate sulphatase from human placenta.On the possible hydrolysis of the alpha-L-iduronide linkage by beta-D-glucuronidase (Ec 3.2.1.31).Neurochemistry of the mucopolysaccharidoses: brain lipids and lysosomal enzymes in patients with four types of mucopolysaccharidosis and in normal controls.Characterization of proteins structurally related to human N-acetyl-beta-D-glucosaminidase.The catabolism of intravenously injected heparan N-[35S] sulphate in the rat.Hepatic storage of glycosaminoglycans in feline and canine models of mucopolysaccharidoses I, VI, and VII.Rat heparins. A study of the relative sizes and antithrombin-binding characteristics of heparin proteoglycans, chains and depolymerization products from rat adipose tissue, heart, lungs, peritoneal cavity and skinDesign and synthesis of substrates for newborn screening of Maroteaux-Lamy and Morquio A syndromes.Protein Complexation and pH Dependent Release Using Boronic Acid Containing PEG-Polypeptide Copolymers.Dermatan sulfate is the major glycosaminoglycan synthesized by cultured guinea pig skin fibroblasts.
P2860
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P2860
description
1976 nî lūn-bûn
@nan
1976年の論文
@ja
1976年論文
@yue
1976年論文
@zh-hant
1976年論文
@zh-hk
1976年論文
@zh-mo
1976年論文
@zh-tw
1976年论文
@wuu
1976年论文
@zh
1976年论文
@zh-cn
name
The mucopolysaccharidoses (a review).
@ast
The mucopolysaccharidoses (a review).
@en
type
label
The mucopolysaccharidoses (a review).
@ast
The mucopolysaccharidoses (a review).
@en
prefLabel
The mucopolysaccharidoses (a review).
@ast
The mucopolysaccharidoses (a review).
@en
P2860
P356
P1476
The mucopolysaccharidoses (a review).
@en
P2093
P2860
P304
P356
10.1073/PNAS.73.2.630
P407
P577
1976-02-01T00:00:00Z