Pages that link to "Q35986296"
Jump to navigation
Jump to search
The following pages link to The mucopolysaccharidoses (a review). (Q35986296):
Displaying 50 items.
- Sanfilippo syndrome type C: deficiency of acetyl-CoA:alpha-glucosaminide N-acetyltransferase in skin fibroblasts (Q24616088) (← links)
- Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency (Q24626591) (← links)
- High performance liquid chromatographic strategy for the analysis of exopolysaccharides extracted from pathogenic bacteria (Q31094395) (← links)
- A new type of bacterial sulfatase reveals a novel maturation pathway in prokaryotes (Q33246408) (← links)
- Oxidative depolymerization of polysaccharides by reactive oxygen/nitrogen species (Q34661527) (← links)
- Heritable Disorders of Connective Tissue: Ehlers-Danlos Syndrome (Q34690884) (← links)
- Arterial pathology in canine mucopolysaccharidosis-I and response to therapy (Q34883690) (← links)
- Glycosaminoglycans in the human cornea: age-related changes (Q35027316) (← links)
- Morphologic and biochemical studies of canine mucopolysaccharidosis I (Q35858094) (← links)
- The pathology of the feline model of mucopolysaccharidosis VI. (Q35863589) (← links)
- Animal model of human disease: Mucopolysaccharidosis VI Maroteaux-Lamy syndrome, Arylsulfatase B-deficient mucopolysaccharidosis in the Siamese cat (Q35864243) (← links)
- Canine alpha-L-iduronidase deficiency. A model of mucopolysaccharidosis I (Q35885212) (← links)
- The pathology of the feline model of mucopolysaccharidosis I (Q35885815) (← links)
- Suramin-induced storage disease. Mucopolysaccharidosis. (Q35885982) (← links)
- Experimental animal model for mucopolysaccharidosis: suramin-induced glycosaminoglycan and sphingolipid accumulation in the rat. (Q36395296) (← links)
- The Synthesis of Glycosaminoglycans by Cultures of Corneal Stromal Cells from Patients with Keratoconus (Q37036937) (← links)
- Spondyloepiphyseal dysplasias and bilateral legg-calvé-perthes disease: diagnostic considerations for mucopolysaccharidoses (Q37127617) (← links)
- Purine receptor antagonist modulates serology and affective behaviors in lupus-prone mice: evidence of autoimmune-induced pain? (Q37440064) (← links)
- Liver-Directed Human Amniotic Epithelial Cell Transplantation Improves Systemic Disease Phenotype in Hurler Syndrome Mouse Model (Q38741428) (← links)
- Prenatal Diagnosis of Inborn Errors of Metabolism (Q39144558) (← links)
- Biochemical and genetic factors in the heat inactivation of murine ?-glucuronidase (Q39171362) (← links)
- Purification and properties of N-acetylgalactosamine 6-sulphate sulphatase from human placenta (Q39273264) (← links)
- On the possible hydrolysis of the α-L-iduronide linkage by β-D-glucuronidase (EC 3.2.1.31) (Q39274870) (← links)
- Neurochemistry of the mucopolysaccharidoses: brain lipids and lysosomal enzymes in patients with four types of mucopolysaccharidosis and in normal controls (Q39601610) (← links)
- Characterization of proteins structurally related to human N-acetyl-β-d-glucosaminidase (Q39617289) (← links)
- α-l-Iduronidase, β-d-glucuronidase, and 2-sulfo-l-iduronate 2-sulfutase: preparation and characterization of radioactive substrates from heparin (Q39654390) (← links)
- Clinical and metabolic aspects of sulfohydrolases in man. (Q39668163) (← links)
- The catabolism of intravenously injected heparan N-[35S]sulphate in the rat (Q39840526) (← links)
- A New Biochemical Subtype of the Sanfilippo Syndrome: Characterization of the Storage Material in Cultured Fibroblasts of Sanfilippo C Patients (Q39874305) (← links)
- Animal models of dwarfism (Q40207883) (← links)
- Influence of glycosaminoglycan synthesis of cultured cornea stroma cells by variation of culture condition (Q40725081) (← links)
- Hepatic storage of glycosaminoglycans in feline and canine models of mucopolysaccharidoses I, VI, and VII. (Q41121360) (← links)
- Mucopolysaccharidosis type I, II, IIIA and V. Pathological and biochemical abnormalities in the neural and mesenchymal elements of the brain (Q41306673) (← links)
- A new variety of spondyloepiphyseal dysplasia characterized by punctate corneal dystrophy and abnormal dermal collagen fibrils (Q41366538) (← links)
- 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 skin (Q41837519) (← links)
- Design and synthesis of substrates for newborn screening of Maroteaux-Lamy and Morquio A syndromes (Q42422146) (← links)
- Protein Complexation and pH Dependent Release Using Boronic Acid Containing PEG-Polypeptide Copolymers (Q44805646) (← links)
- Dermatan sulfate is the major glycosaminoglycan synthesized by cultured guinea pig skin fibroblasts (Q46503567) (← links)
- Taiwan National Newborn Screening Program by Tandem Mass Spectrometry for Mucopolysaccharidoses Types I, II, and VI (Q58607725) (← links)
- Proton conductivity of glycosaminoglycans (Q64117752) (← links)
- Intercellular transfer of β-glucuronidase in chimeric mice (Q66993823) (← links)
- Selective depolymerisation of heparin to produce radio-labelled substrates for sulfamidase, 2-acetamido-2-deoxy-alpha-D-glucosidase, acetyl-CoA:2-amino-2-deoxy-alpha-D-glucoside N-acetyltransferase, and 2-acetamido-2-deoxy-D-glucose 6-sulfate sulfat (Q70159079) (← links)
- Methods for analysis of urinary glycosaminoglycans (Q70236583) (← links)
- The mucopolysaccharidoses: biochemistry and clinical symptoms (Q70554694) (← links)
- Caprine beta-mannosidosis. Inherited deficiency of beta-D-mannosidase (Q70764611) (← links)
- Growth plate pathology in feline mucopolysaccharidosis VI (Q70934305) (← links)
- Electron microscopy: a method for the diagnosis of inherited metabolic storage diseases. Electron microscopy in diagnosis (Q71530432) (← links)
- Separation of reduced disaccharides derived from glycosaminoglycans by high-performance liquid chromatography (Q71563329) (← links)
- Dwarfism in the Alaskan Malamute: ultrastructural features of dwarf growth plate chondrocytes (Q71732796) (← links)
- Characterization of cyclic AMP-resistant Chinese hamster ovary cell mutants lacking type I protein kinase (Q72876008) (← links)