about
Steroid receptor RNA activator protein binds to and counteracts SRA RNA-mediated activation of MyoD and muscle differentiationDnmt3b Prefers Germ Line Genes and Centromeric Regions: Lessons from the ICF Syndrome and Cancer and Implications for DiseasesWhen one is better than two: RNA with dual functionsGermline genes hypomethylation and expression define a molecular signature in peripheral blood of ICF patients: implications for diagnosis and etiology.Dnmt3b recruitment through E2F6 transcriptional repressor mediates germ-line gene silencing in murine somatic tissuesNuclear relocation of a transactivator subunit precedes target gene activation.Identification of potentially new bifunctional RNA based on genome-wide data-mining of alternative splicing events.Long-distance control of origin choice and replication timing in the human beta-globin locus are independent of the locus control region.MafG sumoylation is required for active transcriptional repression.Accumulation of small murine minor satellite transcripts leads to impaired centromeric architecture and function.Mammalian introns: when the junk generates molecular diversity.Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndromeTelomeres in ICF syndrome cells are vulnerable to DNA damage due to elevated DNA:RNA hybridsThree novel ZBTB24 mutations identified in Japanese and Cape Verdean type 2 ICF syndrome patients.Preferential association of irreversibly silenced E2F-target genes with pericentromeric heterochromatin in differentiated muscle cells.Non-coding murine centromeric transcripts associate with and potentiate Aurora B kinaseDynamic changes in transcription factor complexes during erythroid differentiation revealed by quantitative proteomics.Genetic, Cellular and Clinical Features of ICF Syndrome: a French National Survey.Identification of a dinucleotide signature that discriminates coding from non-coding long RNAs.Corrigendum: Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndromeShort intron-derived ncRNAsCENP-A chromatin disassembly in stressed and senescent murine cells.Chromatin modifications in hematopoietic multipotent and committed progenitors are independent of gene subnuclear positioning relative to repressive compartments.A functional enhancer suppresses silencing of a transgene and prevents its localization close to centrometric heterochromatin.Maintenance of DNA methylation: Dnmt3b joins the dance.[Heterochromatin compartments and gene silencing: human hematopoietic differentiation as a model study].Coding or non-coding: Need they be exclusive?Genetics meets DNA methylation in rare diseasesMultiple information carried by RNAs: total eclipse or a light at the end of the tunnel?
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description
hulumtuese
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հետազոտող
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Claire Francastel
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Claire Francastel
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Claire Francastel
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Claire Francastel
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Claire Francastel
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Claire Francastel
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Claire Francastel
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Claire Francastel
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Claire Francastel
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Claire Francastel
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Claire Francastel
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Claire Francastel
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Claire Francastel
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Claire Francastel
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Claire Francastel
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P106
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6603149524
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0000-0002-6353-4320