Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymes.
about
Sanfilippo A disease in the fetus.Mucopolysaccharidoses and mucolipidoses.Secondary storage of dermatan sulfate in Sanfilippo disease.Neurobiology and cellular pathogenesis of glycolipid storage diseases.Secondary lipid accumulation in lysosomal disease.Immunological studies of beta galactosidase in normal human liver and in GM1 gangliosidosisMorphologic and biochemical studies of canine mucopolysaccharidosis I.Endothelium modifies the altered metabolism of the injured aortic wall.Enhancement of cholesterol and cholesteryl ester accumulation in re-endothelialized aorta.The pathology of the feline model of mucopolysaccharidosis VI.Biochemical and histopathological studies on patients with mucopolysaccharidoses, two of whom had been treated by fibroblast transplantationGloboid cell leukodystrophy: deficiency of lactosyl ceramide beta-galactosidase.Inhibition of leucocytic lysosomal enzymes by glycosaminoglycans in vitro.Neurochemistry of the mucopolysaccharidoses: brain lipids and lysosomal enzymes in patients with four types of mucopolysaccharidosis and in normal controls.Neurochemical abnormality in I-cell disease: chemical analysis and a possible importance of beta-galactosidase deficiency.Neurochemistry of the mucopolysaccharidoses: brain glycosaminoglycans in normals and four types of mucopolysaccharidoses.Linkage of genetic determinants for mouse beta-galactosidase electrophoresis and activity.The inhibition of glucosylceramide beta-glucosidase and other acid hydrolases by nucleic acids.The influence of the type of sulphate bond and degree of sulphation of glycosaminoglycans on their interaction with lysosomal enzymes.A quantitative study of pinocytosis and lysosome function in experimentally induced lysosomal storage.Numerous transcriptional alterations in liver persist after short-term enzyme-replacement therapy in a murine model of mucopolysaccharidosis type VII.Enzymic studies of sulphatases in tissues of the normal human and in metachromatic leukodystrophy with multiple sulphatase deficiencies: arylsulphatases A, B and C, cerebroside sulphatase, psychosine sulphatase and steroid sulphatases.Brain sphingolipids in I cell disease (mucolipidosis II).
P2860
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P2860
Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymes.
description
1973 nî lūn-bûn
@nan
1973年の論文
@ja
1973年学术文章
@wuu
1973年学术文章
@zh
1973年学术文章
@zh-cn
1973年学术文章
@zh-hans
1973年学术文章
@zh-my
1973年学术文章
@zh-sg
1973年學術文章
@yue
1973年學術文章
@zh-hant
name
Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymes.
@en
Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymes.
@nl
type
label
Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymes.
@en
Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymes.
@nl
prefLabel
Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymes.
@en
Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymes.
@nl
P2093
P1433
P1476
Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymes.
@en
P2093
P304
P356
10.1126/SCIENCE.181.4097.352
P407
P577
1973-07-01T00:00:00Z