X-chromosome inactivation: molecular mechanisms and genetic consequences.
about
Mammalian homologues of the Polycomb-group gene Enhancer of zeste mediate gene silencing in Drosophila heterochromatin and at S. cerevisiae telomeresSynergism of Xist RNA, DNA methylation, and histone hypoacetylation in maintaining X chromosome inactivationFaithful chromosome transmission requires Spt4p, a putative regulator of chromatin structure in Saccharomyces cerevisiae.An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndromeA cre-transgenic mouse strain for the ubiquitous deletion of loxP-flanked gene segments including deletion in germ cellsThe X chromosome is organized into a gene-rich outer rim and an internal core containing silenced nongenic sequencesAntisense transcription through the Xist locus mediates Tsix function in embryonic stem cells.The dominance theory of Haldane's ruleX chromosome-linked IRAK-1 polymorphism is a strong predictor of multiple organ failure and mortality postinjury.Baculovirus-mediated expression and characterization of the full-length murine DNA methyltransferase.Induction of XIST expression from the human active X chromosome in mouse/human somatic cell hybrids by DNA demethylationA DNA insulator prevents repression of a targeted X-linked transgene but not its random or imprinted X inactivation.Functional interaction between PARP-1 and PARP-2 in chromosome stability and embryonic development in mouseStructural adaptations in the interaction of EcoRI endonuclease with methylated GAATTC sites.The beta-globin locus control region enhances transcription of but does not confer position-independent expression onto the lacZ gene in transgenic mice.Racial disparities and sex-based outcomes differences after severe injury.Sir2 deacetylates histone H3 lysine 56 to regulate telomeric heterochromatin structure in yeast.Evaluation of X-Chromosome Inactivation Patterns in Patients with Acute Myeloid Leukemia during RemissionThe Igf2/H19 imprinting control region exhibits sequence-specific and cell-type-dependent DNA methylation-mediated repression.Non-random X chromosome inactivation in Aicardi syndrome.Skewing of X chromosome inactivation in autoimmunity.Dynamic methylation adjustment and counting as part of imprinting mechanisms.Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse.Connexin 32 mutations from X-linked Charcot-Marie-Tooth disease patients: functional defects and dominant negative effects.DNA of Drosophila melanogaster contains 5-methylcytosine.Genomic structure of the human DNA methyltransferase gene.Rates of evolution of hybrid inviability in birds and mammals.Genome-wide oxidative bisulfite sequencing identifies sex-specific methylation differences in the human placenta.Lyonization effects of the t(X;16) translocation on the phenotypic expression in a rare female with Menkes disease.Developmentally-regulated changes of Xist RNA levels in single preimplantation mouse embryos, as revealed by quantitative real-time PCR.Genome evolution. Global methylation in eutherian hybrids.On the Substrate Specificity of DNA Methyltransferases
P2860
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P2860
X-chromosome inactivation: molecular mechanisms and genetic consequences.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
X-chromosome inactivation: molecular mechanisms and genetic consequences.
@en
type
label
X-chromosome inactivation: molecular mechanisms and genetic consequences.
@en
prefLabel
X-chromosome inactivation: molecular mechanisms and genetic consequences.
@en
P1433
P1476
X-chromosome inactivation: molecular mechanisms and genetic consequences.
@en
P2093
P304
P356
10.1016/0168-9525(94)90169-4
P577
1994-07-01T00:00:00Z