| scholarly article | Q13442814 |
| P2093 | author name string | Chandrasekhar Kanduri | |
| Rolf Ohlsson | |||
| Anita Göndör | |||
| Helene Thomassin | |||
| Meena Kanduri | |||
| Noopur Thakur | |||
| Radha Raman Pandey | |||
| Thierry Grange | |||
| Vijay Kumar Tiwari | |||
| P2860 | cites work | Bidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genes | Q24600595 |
| RNAi-mediated targeting of heterochromatin by the RITS complex | Q24623437 | ||
| A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome | Q24644175 | ||
| Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome | Q24678326 | ||
| Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting | Q24684284 | ||
| Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse | Q28142099 | ||
| CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus | Q28145756 | ||
| Regulation of heterochromatic silencing and histone H3 lysine-9 methylation by RNAi | Q28218870 | ||
| Two classes of short interfering RNA in RNA silencing | Q28219196 | ||
| The non-coding Air RNA is required for silencing autosomal imprinted genes | Q28504980 | ||
| Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain | Q28510861 | ||
| Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1 | Q28589840 | ||
| Tsix, a gene antisense to Xist at the X-inactivation centre | Q33857857 | ||
| LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids | Q33864988 | ||
| Loss of CpG methylation is strongly correlated with loss of histone H3 lysine 9 methylation at DMR-LIT1 in patients with Beckwith-Wiedemann syndrome. | Q33906102 | ||
| Chromosomal silencing and localization are mediated by different domains of Xist RNA. | Q34108304 | ||
| Heterochromatic silencing and HP1 localization in Drosophila are dependent on the RNAi machinery | Q34293738 | ||
| Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. | Q35211749 | ||
| In vivo footprinting of the interaction of proteins with DNA and RNA. | Q38349080 | ||
| Insulator and silencer sequences in the imprinted region of human chromosome 11p15.5. | Q38352362 | ||
| A differentially methylated imprinting control region within the Kcnq1 locus harbors a methylation-sensitive chromatin insulator | Q40747050 | ||
| Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome | Q40859099 | ||
| The 5' flank of mouse H19 in an unusual chromatin conformation unidirectionally blocks enhancer-promoter communication | Q40881417 | ||
| Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function. | Q47590866 | ||
| A differentially methylated region within the gene Kcnq1 functions as an imprinted promoter and silencer | Q48262708 | ||
| Primary non-random X inactivation associated with disruption of Xist promoter regulation. | Q52542452 | ||
| The imprinted antisense RNA at the Igf2r locus overlaps but does not imprint Mas1 | Q73765902 | ||
| Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive | Q74014247 | ||
| Bidirectional silencing and DNA methylation-sensitive methylation-spreading properties of the Kcnq1 imprinting control region map to the same regions | Q78744801 | ||
| P433 | issue | 18 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | cell biology | Q7141 |
| Potassium voltage-gated channel, subfamily Q, member 1 | Q14865158 | ||
| CCCTC-binding factor | Q14908017 | ||
| P304 | page(s) | 7855-62 | |
| P577 | publication date | 2004-09-01 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | An antisense RNA regulates the bidirectional silencing property of the Kcnq1 imprinting control region | |
| P478 | volume | 24 |
| Q28066790 | A lncRNA Perspective into (Re)Building the Heart |
| Q36949891 | A novel H19 antisense RNA overexpressed in breast cancer contributes to paternal IGF2 expression |
| Q34115325 | A novel antisense long noncoding RNA within the IGF1R gene locus is imprinted in hematopoietic malignancies |
| Q35856728 | Allele-specific binding of CTCF to the multipartite imprinting control region KvDMR1 |
| Q40189832 | Alternately spliced WT1 antisense transcripts interact with WT1 sense RNA and show epigenetic and splicing defects in cancer |
| Q42140813 | Alternative mechanisms associated with silencing of CDKN1C in Beckwith-Wiedemann syndrome |
| Q39002254 | An intragenic long noncoding RNA interacts epigenetically with the RUNX1 promoter and enhancer chromatin DNA in hematopoietic malignancies |
| Q37962020 | Antisense RNAs and epigenetic regulation |
| Q35942449 | Bsr, a nuclear-retained RNA with monoallelic expression |
| Q35764211 | Chromatin-Mediated Reversible Silencing of Sense-Antisense Gene Pairs in Embryonic Stem Cells Is Consolidated upon Differentiation |
| Q29615417 | DNA methylation and human disease |
| Q63352567 | Differential methylation of the type 2 diabetes susceptibility locus KCNQ1 is associated with insulin sensitivity and is predicted by CpG site specific genetic variation |
| Q34320111 | Differentiation-driven nucleolar association of the mouse imprinted Kcnq1 locus |
| Q36527441 | Dosage compensation, the origin and the afterlife of sex chromosomes |
| Q24546155 | Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes |
| Q35097959 | Enhancers compete with a long non-coding RNA for regulation of the Kcnq1 domain |
| Q37789745 | Epigenetic aspects of fertilization and preimplantation development in mammals: lessons from the mouse. |
| Q33338682 | Evolution of the CDKN1C-KCNQ1 imprinted domain |
| Q34565169 | Expression profile of LIT1/KCNQ1OT1 and epigenetic status at the KvDMR1 in colorectal cancers. |
| Q55440696 | Genome-wide analysis of long non-coding RNAs affecting roots development at an early stage in the rice response to cadmium stress. |
| Q35898187 | Genome-wide analysis of long non-coding RNAs at early stage of skin pigmentation in goats (Capra hircus). |
| Q35630476 | Genome-wide natural antisense transcription: coupling its regulation to its different regulatory mechanisms |
| Q21184167 | Genome-wide prediction and identification of cis-natural antisense transcripts in Arabidopsis thaliana |
| Q30698865 | Grabbing the genome by the NADs |
| Q37683453 | H2A.B facilitates transcription elongation at methylated CpG loci |
| Q81515696 | Highly expressed genes are associated with inverse antisense transcription in mouse |
| Q41678364 | How do lncRNAs regulate transcription? |
| Q34507207 | Imprinting disruption of the CDKN1C/KCNQ1OT1 domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer. |
| Q36635375 | Insights into the molecular mechanism for type 2 diabetes susceptibility at the KCNQ1 locus from temporal changes in imprinting status in human islets. |
| Q24641815 | Kcnq1ot1/Lit1 noncoding RNA mediates transcriptional silencing by targeting to the perinucleolar region |
| Q35025042 | Limited evolutionary conservation of imprinting in the human placenta |
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| Q37441308 | Long noncoding RNA-mediated intrachromosomal interactions promote imprinting at the Kcnq1 locus. |
| Q38824250 | Long noncoding RNAs in kidney and cardiovascular diseases |
| Q24655701 | Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation |
| Q37365817 | Loss of imprinting of insulin-like growth factor 2 is associated with increased risk of lymph node metastasis and gastric corpus cancer |
| Q46067277 | Making sense of Dlx1 antisense RNA. |
| Q37831991 | Molecular mechanisms of genomic imprinting and clinical implications for cancer |
| Q37401175 | Monoallelic gene expression in mammals. |
| Q40508899 | NF-Y regulates the antisense promoter, bidirectional silencing, and differential epigenetic marks of the Kcnq1 imprinting control region |
| Q47118105 | Natural Antisense Transcripts at the Interface between Host Genome and Mobile Genetic Elements |
| Q50006887 | Natural antisense transcripts in diseases: From modes of action to targeted therapies. |
| Q36288741 | Natural antisense transcripts: sound or silence? |
| Q28732315 | Non coding RNAs and viruses in the framework of the phylogeny of the genes, epigenesis and heredity |
| Q34749691 | Non-coding RNAs in imprinted gene clusters |
| Q101464954 | Non-coding RNAs: The key detectors and regulators in cardiovascular disease |
| Q35139414 | Nonallelic transcriptional roles of CTCF and cohesins at imprinted loci. |
| Q34014009 | Noncoding RNA in development |
| Q38816280 | Noncoding RNAs in smooth muscle cell homeostasis: implications in phenotypic switch and vascular disorders |
| Q40355171 | PEG3 domain gene expression in maternal and foetal placenta in intrauterine growth restricted bovine foetuses |
| Q35781651 | Painting of fourth and chromosome-wide regulation of the 4th chromosome in Drosophila melanogaster |
| Q27000736 | Perspectives on the mechanism of transcriptional regulation by long non-coding RNAs |
| Q46643638 | Processing of naturally occurring sense/antisense transcripts of the vertebrate Slc34a gene into short RNAs |
| Q35077134 | Regulated antisense transcription controls expression of cell-type-specific genes in yeast |
| Q46090697 | Regulation of antisense RNA expression during cardiac MHC gene switching in response to pressure overload |
| Q35098964 | Role of genomic architecture in the expression dynamics of long noncoding RNAs during differentiation of human neuroblastoma cells |
| Q34028303 | Shaping the Genome with Non-Coding RNAs |
| Q30481382 | Small RNAs and the regulation of cis-natural antisense transcripts in Arabidopsis. |
| Q36491208 | Spatial Organization of Epigenomes |
| Q24648944 | Specific expression of long noncoding RNAs in the mouse brain |
| Q37873983 | The central role of RNA in human development and cognition |
| Q21092463 | The genetic signatures of noncoding RNAs |
| Q53001244 | The imprinted mouse Igf2r/Air cluster--a model maternal imprinting system. |
| Q36088917 | The influence of non-coding RNAs on allele-specific gene expression in mammals |
| Q40289583 | The length of the transcript encoded from the Kcnq1ot1 antisense promoter determines the degree of silencing |
| Q26997073 | The research strategies for probing the function of long noncoding RNAs |
| Q22121998 | The rise of regulatory RNA |
| Q34079400 | The role of long non-coding RNAs in neurodevelopment, brain function and neurological disease |
| Q35113579 | The silence RNA keeps: cis mechanisms of RNA mediated epigenetic silencing in mammals |
| Q58134238 | The two-domain hypothesis in Beckwith–Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster |
| Q36392021 | Two distinct mechanisms of silencing by the KvDMR1 imprinting control region |
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