Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency.

scientific article published on January 1985

Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency. is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1004652728
P356DOI10.1007/BF00295367
P698PubMed publication ID3860470

P50authorAndrea BallabioQ28008372
P2093author name stringG Andria
P Di Natale
G Parenti
E Napolitano
P2860cites workProtein measurement with the Folin phenol reagentQ20900776
Genetic complementation studies of multiple sulfatase deficiencyQ33989276
Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblastsQ36412160
X-linked ichthyosis due to steroid-sulphatase deficiencyQ39471869
Is multiple sulphatase deficiency due to defective regulation of sulphohydrolase expression?Q39695657
Correction of I-cell defect by hybridization with lysosomal enzyme deficient human fibroblasts.Q40656691
Production of mammalian somatic cell hybrids by means of polyethylene glycol treatmentQ67429981
Steroid sulphatase deficiency. Steroid sulphatase and arylsulphatase C determination in normal and affected fibroblastsQ70499124
Enhanced breakdown of arylsulfatase A in multiple sulfatase deficiencyQ72525562
Biochemical variability of arylsulphatases‐A,‐B and‐C in cultured fibroblasts from patients with multiple sulphatase deficiencyQ72573360
Mucopolysaccharidosis III B: hybridization studies on fibroblasts from a mild case and fibroblasts from severe patientsQ72809864
P433issue4
P921main subjectX-linked ichthyosisQ3804555
P304page(s)315-317
P577publication date1985-01-01
P1433published inHuman GeneticsQ5937167
P1476titleGenetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency
P478volume70

Reverse relations

cites work (P2860)
Q24314592A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy
Q69312665A fluorimetric assay of steroid sulphatase in leukocytes: evidence for two genetically different enzymes with arylsulphatase C activity
Q41544332A high resolution deletion map of human chromosome Xp22.
Q35131653A major step on the road to understanding a unique posttranslational modification and its role in a genetic disease
Q41965319Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiency
Q34180405Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndrome
Q52192475Ichthyosis: the skin manifestation of multiple sulfatase deficiency.
Q24675965Identification of point mutations in the steroid sulfatase gene of three patients with X-linked ichthyosis
Q24605693Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis
Q36909307Multiple sulfatase deficiency: catalytically inactive sulfatases are expressed from retrovirally introduced sulfatase cDNAs
Q28646261The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases
Q59287993X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome