Cloning and expression of steroid sulfatase cDNA and the frequent occurrence of deletions in STS deficiency: implications for X-Y interchange
about
Studying early lethality of 45,XO (Turner's syndrome) embryos using human embryonic stem cellsCharacterization of point mutations in patients with X-linked ichthyosis. Effects on the structure and function of the steroid sulfatase proteinSulfatases and sulfatase modifying factors: an exclusive and promiscuous relationshipAnalysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinismBiochemical characterization of arylsulfatase E and functional analysis of mutations found in patients with X-linked chondrodysplasia punctataHunter syndrome: isolation of an iduronate-2-sulfatase cDNA clone and analysis of patient DNASelection of a subset of mRNAs from combinatorial 3' untranslated region libraries using neuronal RNA-binding protein Hel-N1Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosomeThe molecular biology, biochemistry, and physiology of human steroidogenesis and its disordersCloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosisDeletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplificationAbsence of methylation of a CpG-rich region at the 5' end of the MIC2 gene on the active X, the inactive X, and the Y chromosomeAdrenoleukodystrophy: a complex chromosomal rearrangement in the Xq28 red/green-color-pigment gene region indicates two possible gene localizationsIdentification of point mutations in the steroid sulfatase gene of three patients with X-linked ichthyosisAn Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometrySUMF1 enhances sulfatase activities in vivo in five sulfatase deficienciesAndrogen biosynthesis in castration-resistant prostate cancerPurification and characterization of the arylsulfatase synthesized by Pseudomonas aeruginosa PAO during growth in sulfate-free medium and cloning of the arylsulfatase gene (atsA)Cloning of the rat steroid sulfatase gene (Sts), a non-pseudoautosomal X-linked gene that undergoes X inactivationA cDNA clone for human glucosamine-6-sulphatase reveals differences between arylsulphatases and non-arylsulphatasesThe evolutionary conservation of a novel protein modification, the conversion of cysteine to serinesemialdehyde in arylsulfatase from Volvox carteriTwo site-directed mutations abrogate enzyme activity but have different effects on the conformation and cellular content of the N-acetylgalactosamine 4-sulphatase proteinX/Y translocations resulting from recombination between homologous sequences on Xp and Yq.Gene therapy and dermatology: more than just skin deep.X-linked ichthyosis: an update.Exchange of terminal portions of X- and Y-chromosomal short arms in human XY femalesThe human Y chromosome, in the light of evolution.Molecular studies of deletions at the human steroid sulfatase locus.A model of corrective gene transfer in X-linked ichthyosis.Linkage of the murine steroid sulfatase locus, Sts, to sex reversed, Sxr: a genetic and molecular analysis.A short pseudoautosomal region in laboratory mice.Characterization of a low copy repetitive element S232 involved in the generation of frequent deletions of the distal short arm of the human X chromosomeA multipoint linkage map of the distal short arm of the human X chromosome.The human arylsulfatase-C isoenzymes: two distinct genes that escape from X inactivation.Steroid sulfatase gene in XX males.Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivation.Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutA long range restriction map of the distal human X chromosome short arm around the steroid sulfatase locus.An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome.Matching the Diversity of Sulfated Biomolecules: Creation of a Classification Database for Sulfatases Reflecting Their Substrate Specificity.
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P2860
Cloning and expression of steroid sulfatase cDNA and the frequent occurrence of deletions in STS deficiency: implications for X-Y interchange
description
1987 nî lūn-bûn
@nan
1987 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
Cloning and expression of ster ...... plications for X-Y interchange
@ast
Cloning and expression of ster ...... plications for X-Y interchange
@en
Cloning and expression of ster ...... plications for X-Y interchange
@nl
type
label
Cloning and expression of ster ...... plications for X-Y interchange
@ast
Cloning and expression of ster ...... plications for X-Y interchange
@en
Cloning and expression of ster ...... plications for X-Y interchange
@nl
prefLabel
Cloning and expression of ster ...... plications for X-Y interchange
@ast
Cloning and expression of ster ...... plications for X-Y interchange
@en
Cloning and expression of ster ...... plications for X-Y interchange
@nl
P2093
P3181
P1433
P1476
Cloning and expression of ster ...... plications for X-Y interchange
@en
P2093
L J Shapiro
R T Taggart
T Mohandas
P304
P3181
P356
10.1016/0092-8674(87)90447-8
P407
P577
1987-05-22T00:00:00Z