scholarly article | Q13442814 |
P819 | ADS bibcode | 1980PNAS...77.6166C |
P356 | DOI | 10.1073/PNAS.77.10.6166 |
P8608 | Fatcat ID | release_a4nin66hx5cnfojvrdrwdcfbje |
P953 | full work available at URL | https://europepmc.org/articles/PMC350235 |
https://europepmc.org/articles/PMC350235?pdf=render | ||
https://pnas.org/doi/pdf/10.1073/pnas.77.10.6166 | ||
P932 | PMC publication ID | 350235 |
P698 | PubMed publication ID | 6108562 |
P5875 | ResearchGate publication ID | 17076873 |
P2093 | author name string | P. L. Chang | |
R. G. Davidson | |||
P2860 | cites work | Protein measurement with the Folin phenol reagent | Q20900776 |
Interallelic Complementation in Hybrid Cells Derived from Human Diploid Strains Deficient in Galactose-1-Phosphate Uridyl Transferase Activity | Q33707240 | ||
Genetic complementation studies of multiple sulfatase deficiency | Q33989276 | ||
Xeroderma pigmentosum: biochemical and genetic characteristics | Q34087613 | ||
Protein Complementation | Q35010244 | ||
Genetic complementation in heterokaryons of human fibroblasts defective in cobalamin metabolism | Q35086355 | ||
Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosis | Q35201166 | ||
Arysulfatase A modulation with pH in multiple sulfatase deficiency disorder fibroblasts | Q35203477 | ||
Electrophoresis of arylsulfatase from normal individuals and patients with metachromatic leukodystrophy | Q35569992 | ||
A sensitive fluorescence assay for the simultaneous and separate determination of arylsulphatases A and B | Q39159008 | ||
Immunologic Studies of Arylsulfatase A in Normal and Metachromatic Leukodystrophy Liver | Q39189371 | ||
An improved method for arylsulfatase a detection on polyacrylamide slab gels | Q39522809 | ||
Intergenic complementation after fusion of fibroblasts from different patients with β-galactosidase deficiency | Q39638605 | ||
Is multiple sulphatase deficiency due to defective regulation of sulphohydrolase expression? | Q39695657 | ||
Complementation at the molecular level of enzyme interaction | Q40026618 | ||
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 | Q43570481 | ||
Beta-galactosidase deficient-type mucolipidosis: A complementation study of neuraminidase in somatic cell hybrids | Q44007899 | ||
Studies in metachromatic leukodystrophy. XII. Multiple sulfatase deficiency | Q44101329 | ||
Multiple sulfatase deficiencies in cultured skin fibroblasts. Occurrence in patients with a variant form of metachromatic leukodystrophy | Q44962658 | ||
Polyethylene glycol-induced mammalian cell hybridization: effect of polyethylene glycol molecular weight and concentration | Q45350313 | ||
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 sedimentation | Q59074490 | ||
Multiple Deficiency of Mucopolysaccharide Sulfatases in Mucosulfatidosis | Q66982275 | ||
Enzyme electrophoresis on cellulose acetate gel. II. Zymogram patterns in man-Chinese hamster somatic cell hybrids | Q68707231 | ||
Comparative heat stability of blood catalase | Q72330483 | ||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | metachromatic leukodystrophy | Q1120682 |
P304 | page(s) | 6166-6170 | |
P577 | publication date | 1980-10-01 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts | |
P478 | volume | 77 |
Q70937066 | A sensitive and dependable assay for distinguishing hamster and human X-linked steroid sulfatase activity in somatic cell hybrids |
Q34248650 | Biochemical aspects of globoid and metachromatic leukodystrophies |
Q72573360 | Biochemical variability of arylsulphatases‐A,‐B and‐C in cultured fibroblasts from patients with multiple sulphatase deficiency |
Q35199889 | Complementation of multiple sulfatase deficiency in somatic cell hybrids |
Q41483368 | Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency. |
Q34707253 | Genetic heterogeneity in metachromatic leukodystrophy |
Q72555844 | Immunofluorescence staining and immunological studies of arylsulphatase a of multiple sulphatase deficiency (MSD) and metachromatic leukodystrophy (MLD) fibroblasts |
Q36909307 | Multiple sulfatase deficiency: catalytically inactive sulfatases are expressed from retrovirally introduced sulfatase cDNAs |
Q37509878 | Pseudo arylsulfatase-A deficiency in healthy individuals: genetic and biochemical relationship to metachromatic leukodystrophy |
Q70601017 | Somatic cell hybridization studies on the genetic regulation and allelic mutations in metachromatic leukodystrophy |
Q28646261 | The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases |