Multiple sulfatase deficiencies in cultured skin fibroblasts. Occurrence in patients with a variant form of metachromatic leukodystrophy.
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Lysosomal arylsulfatase deficiencies in humans: chromosome assignments for arylsulfatase A and BTissue-specific expression of human arylsulfatase-C isozymes and steroid sulfataseGenetic complementation studies of multiple sulfatase deficiency.Biochemical aspects of globoid and metachromatic leukodystrophies.Genetic heterogeneity in metachromatic leukodystrophyThe human arylsulfatase-C isoenzymes: two distinct genes that escape from X inactivation.Complementation of multiple sulfatase deficiency in somatic cell hybridsPlacental steroid deficiency: association with arylsulfatase A deficiency.Presence of arylsulfatase A (ARS A) in multiple sulfatase deficiency disorder fibroblasts.Arysulfatase A modulation with pH in multiple sulfatase deficiency disorder fibroblasts.The mucopolysaccharidoses (a review).Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts.Is multiple sulphatase deficiency due to defective regulation of sulphohydrolase expression?Hair root analysis in X-linked ichthyosis.Overexpression of N-acetylgalactosamine-4-sulphatase induces a multiple sulphatase deficiency in mucopolysaccharidosis-type-VI fibroblasts.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.Multiple sulfatase deficiency with early severe retinal degeneration.Complementation studies with clinical and biochemical characterizations of a new variant of multiple sulphatase deficiency.Chemical compositions of brain and myelin in two patients with multiple sulphatase deficiency (a variant form of metachromatic leukodystrophy).Sulfamidase deficiency in a family of Dachshunds: a canine model of mucopolysaccharidosis IIIA (Sanfilippo A).[Metachromatic leukodystrophy: report of 2 cases with histochemistry of nerves and muscles]Subcellular fractionation and subcellular localization of aminopeptidase N in the rabbit enterocytes
P2860
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P2860
Multiple sulfatase deficiencies in cultured skin fibroblasts. Occurrence in patients with a variant form of metachromatic leukodystrophy.
description
1974 nî lūn-bûn
@nan
1974年の論文
@ja
1974年学术文章
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1974年学术文章
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1974年学术文章
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1974年学术文章
@zh-my
1974年学术文章
@zh-sg
1974年學術文章
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1974年學術文章
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1974年學術文章
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name
Multiple sulfatase deficiencie ...... metachromatic leukodystrophy.
@en
Multiple sulfatase deficiencie ...... metachromatic leukodystrophy.
@nl
type
label
Multiple sulfatase deficiencie ...... metachromatic leukodystrophy.
@en
Multiple sulfatase deficiencie ...... metachromatic leukodystrophy.
@nl
prefLabel
Multiple sulfatase deficiencie ...... metachromatic leukodystrophy.
@en
Multiple sulfatase deficiencie ...... metachromatic leukodystrophy.
@nl
P2093
P1433
P1476
Multiple sulfatase deficiencie ...... metachromatic leukodystrophy.
@en
P2093
Herschkowitz NN
Wiesmann UN
P304
P356
10.1001/ARCHNEUR.1974.00490320041005
P577
1974-02-01T00:00:00Z