Expression of an X-linked gene from an inactive human X chromosome in mouse-human hybrid cells: further evidence for the noninactivation of the steroid sulfatase locus in man.
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Molecular cloning of a novel splice variant of human type IVA (PDE-IVA) cyclic AMP phosphodiesterase and localization of the gene to the p13.2-q12 region of human chromosome 19 [corrected]Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studiesAssignment of the gene for human DNA polymerase alpha to the X chromosomeTissue-specific expression of human arylsulfatase-C isozymes and steroid sulfataseMolecular genetics of the human X chromosome.Extensive DNA sequence homologies between the human Y and the long arm of the X chromosome.Evidence for X-linkage of steroid sulfatase in the mouse: steroid sulfatase levels in oocytes of XX and XO mice.Identification of an autosomal locus affecting steroid sulfatase activity among inbred strains of miceVariable escape from X-chromosome inactivation: identifying factors that tip the scales towards expressionA long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes.The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy.Dosage of the Sts gene in the mouse.Complementation of multiple sulfatase deficiency in somatic cell hybridsFrequency of reactivation and variability in expression of X-linked enzyme lociThe cell surface antigen locus, MIC2X, escapes X-inactivationThe steroid sulfatase locus on structurally abnormal inactive X chromosomes is expressed.Fine mapping of the distal short arm of the human X chromosome using X/Y translocations.Steroid sulfatase gene in XX males.Placental steroid deficiency: association with arylsulfatase A deficiency.Evidence for a dosage effect at the X-linked steroid sulfatase locus in human tissues.Assignment of the functional gene for human adrenodoxin to chromosome 11q13----qter and of adrenodoxin pseudogenes to chromosome 20cen----q13.1.X chromosome inactivation of the human TIMP gene.Differential methylation of hypoxanthine phosphoribosyltransferase genes on active and inactive human X chromosomes.Cell cycle-specific reactivation of an inactive X-chromosome locus by 5-azadeoxycytidineTransformation with DNA from 5-azacytidine-reactivated X chromosomesSpecific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion.Variable numbers of pepsinogen genes are located in the centromeric region of human chromosome 11 and determine the high-frequency electrophoretic polymorphism.Schizophrenia-associated chromosome 11q21 translocation: identification of flanking markers and development of chromosome 11q fragment hybrids as cloning and mapping resources.An assay for X inactivation based on differential methylation at the fragile X locus, FMR1.The great escape.
P2860
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P2860
Expression of an X-linked gene from an inactive human X chromosome in mouse-human hybrid cells: further evidence for the noninactivation of the steroid sulfatase locus in man.
description
1980 nî lūn-bûn
@nan
1980年の論文
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1980年学术文章
@wuu
1980年学术文章
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1980年学术文章
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1980年学术文章
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1980年学术文章
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1980年學術文章
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1980年學術文章
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name
Expression of an X-linked gene ...... teroid sulfatase locus in man.
@ast
Expression of an X-linked gene ...... teroid sulfatase locus in man.
@en
type
label
Expression of an X-linked gene ...... teroid sulfatase locus in man.
@ast
Expression of an X-linked gene ...... teroid sulfatase locus in man.
@en
prefLabel
Expression of an X-linked gene ...... teroid sulfatase locus in man.
@ast
Expression of an X-linked gene ...... teroid sulfatase locus in man.
@en
P2093
P2860
P356
P1476
Expression of an X-linked gene ...... teroid sulfatase locus in man.
@en
P2093
B Hellkuhl
K H Grzeschik
L J Shapiro
R S Sparkes
T Mohandas
P2860
P304
P356
10.1073/PNAS.77.11.6759
P407
P577
1980-11-01T00:00:00Z