Multiple sulfatase deficiencies in cultured skin fibroblasts. Occurrence in patients with a variant form of metachromatic leukodystrophy

scientific article

Multiple sulfatase deficiencies in cultured skin fibroblasts. Occurrence in patients with a variant form of metachromatic leukodystrophy is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1001/ARCHNEUR.1974.00490320041005
P698PubMed publication ID4272659

P2093author name stringCarson JH
Wiesmann UN
Eto Y
Herschkowitz NN
P433issue2
P921main subjectpatientQ181600
P304page(s)153-156
P577publication date1974-02-01
P1433published inArchives of NeurologyQ15766672
P1476titleMultiple sulfatase deficiencies in cultured skin fibroblasts. Occurrence in patients with a variant form of metachromatic leukodystrophy
P478volume30

Reverse relations

cites work (P2860)
Q39242762Adult metachromatic leukodystrophy. Arylsulphatase-A values in four generations of one family and some reflections about the genetics
Q52434608Arylsulfatase A in serum from patients with cancer of various organs
Q41660126Arylsulfatases A and B in EBV-transformed lymphoid cell lines: Studies on their molecular forms in cells from patients with inborn sulfatase deficiencies. Comparative diagnostic value of enzymatic assays
Q39296525Arylsulphatase a and b in juvenile metachromatic leukodystrophy
Q35203477Arysulfatase A modulation with pH in multiple sulfatase deficiency disorder fibroblasts
Q34248650Biochemical aspects of globoid and metachromatic leukodystrophies
Q72531825Biochemical characterization of neonatal multiple sulfatase deficient (MSD) disorder cultured skin fibroblasts
Q72573360Biochemical variability of arylsulphatases‐A,‐B and‐C in cultured fibroblasts from patients with multiple sulphatase deficiency
Q69862567Biosynthesis and intracellular pool of aminopeptidase N in rabbit enterocytes
Q48351485Chemical compositions of brain and myelin in two patients with multiple sulphatase deficiency (a variant form of metachromatic leukodystrophy).
Q72514046Clinicopathological differences between juvenile and late infantile metachromatic leukodystrophy
Q36412160Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts
Q35199889Complementation of multiple sulfatase deficiency in somatic cell hybrids
Q46030873Complementation studies with clinical and biochemical characterizations of a new variant of multiple sulphatase deficiency.
Q66970619Determination of arylsulfatase C in hair follicles
Q72519127Differential assay of arylsulfatase A and B activities: A sensitive method for cultured human cells
Q39717716Enrichment of human heterokaryons by ficoll gradient for complementation analysis of iduronate sulfatase deficiency
Q43570481Enzymic 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
Q33989276Genetic complementation studies of multiple sulfatase deficiency
Q34707253Genetic heterogeneity in metachromatic leukodystrophy
Q41571680Hair root analysis in X-linked ichthyosis
Q43989400Heterogeneity of lysosomes in human fibroblasts
Q72555844Immunofluorescence staining and immunological studies of arylsulphatase a of multiple sulphatase deficiency (MSD) and metachromatic leukodystrophy (MLD) fibroblasts
Q39695657Is multiple sulphatase deficiency due to defective regulation of sulphohydrolase expression?
Q81708372Long-term follow-up of a girl with Maroteaux-Lamy syndrome after bone marrow transplantation
Q24597204Lysosomal arylsulfatase deficiencies in humans: Chromosome assignments for arylsulfatase A and B
Q71435387Multiple sulfatase deficiency (mucosulfatidosis): impaired degradation of labeled sulfated compounds in cultured skin fibroblasts in vivo
Q45222847Multiple sulfatase deficiency with early severe retinal degeneration
Q72488408Multiple sulphatase deficiency with early onset
Q72551199Neonatal multiple sulphatase deficiency disorder biochemical characterization
Q42137916Overexpression of N-acetylgalactosamine-4-sulphatase induces a multiple sulphatase deficiency in mucopolysaccharidosis-type-VI fibroblasts
Q35202242Placental steroid deficiency: association with arylsulfatase A deficiency
Q35202748Presence of arylsulfatase A (ARS A) in multiple sulfatase deficiency disorder fibroblasts
Q57042255Subcellular fractionation and subcellular localization of aminopeptidase N in the rabbit enterocytes
Q48429591Sulfamidase deficiency in a family of Dachshunds: a canine model of mucopolysaccharidosis IIIA (Sanfilippo A).
Q35197993The human arylsulfatase-C isoenzymes: two distinct genes that escape from X inactivation
Q35986296The mucopolysaccharidoses (a review).
Q71467168Thiosulfate-mediated increase of arylsulfatase activities in multiple sulfatase deficiency disorder fibroblasts
Q24676239Tissue-specific expression of human arylsulfatase-C isozymes and steroid sulfatase
Q39902084Urinary acid mucopolysaccharides in Multiple Sulfatase Deficiency (Mucosulfatidosis)
Q50942766[Metachromatic leukodystrophy: report of 2 cases with histochemistry of nerves and muscles]