Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts

scientific article published on October 1, 1980

Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts is …
instance of (P31):
scholarly articleQ13442814

External links are
P819ADS bibcode1980PNAS...77.6166C
P356DOI10.1073/PNAS.77.10.6166
P8608Fatcat IDrelease_a4nin66hx5cnfojvrdrwdcfbje
P953full work available at URLhttps://europepmc.org/articles/PMC350235
https://europepmc.org/articles/PMC350235?pdf=render
https://pnas.org/doi/pdf/10.1073/pnas.77.10.6166
P932PMC publication ID350235
P698PubMed publication ID6108562
P5875ResearchGate publication ID17076873

P2093author name stringP. L. Chang
R. G. Davidson
P2860cites workProtein measurement with the Folin phenol reagentQ20900776
Interallelic Complementation in Hybrid Cells Derived from Human Diploid Strains Deficient in Galactose-1-Phosphate Uridyl Transferase ActivityQ33707240
Genetic complementation studies of multiple sulfatase deficiencyQ33989276
Xeroderma pigmentosum: biochemical and genetic characteristicsQ34087613
Protein ComplementationQ35010244
Genetic complementation in heterokaryons of human fibroblasts defective in cobalamin metabolismQ35086355
Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosisQ35201166
Arysulfatase A modulation with pH in multiple sulfatase deficiency disorder fibroblastsQ35203477
Electrophoresis of arylsulfatase from normal individuals and patients with metachromatic leukodystrophyQ35569992
A sensitive fluorescence assay for the simultaneous and separate determination of arylsulphatases A and BQ39159008
Immunologic Studies of Arylsulfatase A in Normal and Metachromatic Leukodystrophy LiverQ39189371
An improved method for arylsulfatase a detection on polyacrylamide slab gelsQ39522809
Intergenic complementation after fusion of fibroblasts from different patients with β-galactosidase deficiencyQ39638605
Is multiple sulphatase deficiency due to defective regulation of sulphohydrolase expression?Q39695657
Complementation at the molecular level of enzyme interactionQ40026618
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 sulphatasesQ43570481
Beta-galactosidase deficient-type mucolipidosis: A complementation study of neuraminidase in somatic cell hybridsQ44007899
Studies in metachromatic leukodystrophy. XII. Multiple sulfatase deficiencyQ44101329
Multiple sulfatase deficiencies in cultured skin fibroblasts. Occurrence in patients with a variant form of metachromatic leukodystrophyQ44962658
Polyethylene glycol-induced mammalian cell hybridization: effect of polyethylene glycol molecular weight and concentrationQ45350313
Enzyme electrophoresis on cellulose acetate gel: zymogram patterns in mgh-mouse and man--Chinese hamster somatic cell hybrids.Q53994380
Genetic complementation after fusion of Tay-Sachs and Sandhoff cells.Q54129199
Tay-Sachs and Sandhoff's disease: intergenic complementation after somatic cell hybridization.Q54565642
Non-selective isolation of human somatic cell hybrids by unit-gravity sedimentationQ59074490
Multiple Deficiency of Mucopolysaccharide Sulfatases in MucosulfatidosisQ66982275
Enzyme electrophoresis on cellulose acetate gel. II. Zymogram patterns in man-Chinese hamster somatic cell hybridsQ68707231
Comparative heat stability of blood catalaseQ72330483
P433issue10
P407language of work or nameEnglishQ1860
P921main subjectmetachromatic leukodystrophyQ1120682
P304page(s)6166-6170
P577publication date1980-10-01
P1433published inProceedings of the National Academy of Sciences of the United States of AmericaQ1146531
P1476titleComplementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts
P478volume77

Reverse relations

cites work (P2860)
Q70937066A sensitive and dependable assay for distinguishing hamster and human X-linked steroid sulfatase activity in somatic cell hybrids
Q34248650Biochemical aspects of globoid and metachromatic leukodystrophies
Q72573360Biochemical variability of arylsulphatases‐A,‐B and‐C in cultured fibroblasts from patients with multiple sulphatase deficiency
Q35199889Complementation of multiple sulfatase deficiency in somatic cell hybrids
Q41483368Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency.
Q34707253Genetic heterogeneity in metachromatic leukodystrophy
Q72555844Immunofluorescence staining and immunological studies of arylsulphatase a of multiple sulphatase deficiency (MSD) and metachromatic leukodystrophy (MLD) fibroblasts
Q36909307Multiple sulfatase deficiency: catalytically inactive sulfatases are expressed from retrovirally introduced sulfatase cDNAs
Q37509878Pseudo arylsulfatase-A deficiency in healthy individuals: genetic and biochemical relationship to metachromatic leukodystrophy
Q70601017Somatic cell hybridization studies on the genetic regulation and allelic mutations in metachromatic leukodystrophy
Q28646261The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases