Pages that link to "Q24684284"
Jump to navigation
Jump to search
The following pages link to 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):
Displaying 50 items.
- ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome (Q24301866) (← links)
- Induction of p57(KIP2) expression by p73beta. (Q24531472) (← links)
- In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene (Q24532045) (← links)
- Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control (Q24539092) (← links)
- The Evf-2 noncoding RNA is transcribed from the Dlx-5/6 ultraconserved region and functions as a Dlx-2 transcriptional coactivator (Q24548002) (← links)
- An antisense RNA regulates the bidirectional silencing property of the Kcnq1 imprinting control region (Q24563030) (← links)
- The non-coding RNAs as riboregulators (Q24607004) (← links)
- The Air noncoding RNA: an imprinted cis-silencing transcript (Q24610062) (← links)
- Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19 (Q24615581) (← links)
- Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects (Q24632842) (← links)
- Methylation analysis of KvDMR1 in human oocytes (Q24647913) (← links)
- The human silent information regulator (Sir)2 homologue hSIRT3 is a mitochondrial nicotinamide adenine dinucleotide-dependent deacetylase (Q24671306) (← links)
- Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome (Q24678326) (← links)
- An imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locus (Q24678820) (← links)
- Genomic imprinting and assisted reproduction (Q24793282) (← links)
- Recent Advances in Developing Small Molecules Targeting Nucleic Acid (Q26744202) (← links)
- Nuclear lncRNAs as epigenetic regulators-beyond skepticism (Q26823935) (← links)
- Long noncoding RNAs: past, present, and future (Q26991873) (← links)
- The emergence of lncRNAs in cancer biology (Q27024237) (← links)
- Glypican-3-deficient mice exhibit developmental overgrowth and some of the abnormalities typical of Simpson-Golabi-Behmel syndrome (Q28139404) (← links)
- Frequent loss of imprinting of IGF2 and MEST in lung adenocarcinoma (Q28215251) (← links)
- Allele-specific chromatin immunoprecipitation studies show genetic influence on chromatin state in human genome (Q28469213) (← links)
- Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice (Q28585784) (← links)
- Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1 (Q28589840) (← links)
- Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome (Q28592236) (← links)
- DNA methylation and human disease (Q29615417) (← links)
- Genomic imprinting: parental influence on the genome (Q29616227) (← links)
- The history of cancer epigenetics (Q29617273) (← links)
- Impact of the genome on the epigenome is manifested in DNA methylation patterns of imprinted regions in monozygotic and dizygotic twins (Q31032416) (← links)
- An 11p15 imprinting centre region 2 deletion in a family with Beckwith Wiedemann syndrome provides insights into imprinting control at CDKN1C. (Q31044124) (← links)
- Genome‐Wide Analysis of Epigenetics in Cancer (Q33186874) (← links)
- Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome). (Q33419813) (← links)
- Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects (Q33780868) (← links)
- The Missing lnc(RNA) between the pancreatic β-cell and diabetes (Q33828371) (← links)
- Beckwith-Wiedemann syndrome: imprinting in clusters revisited (Q33838090) (← links)
- The impact of genomic imprinting for neurobehavioral and developmental disorders (Q33843172) (← links)
- Differential methylation persists at the mouse Rasgrf1 DMR in tissues displaying monoallelic and biallelic expression (Q33861237) (← links)
- The uniqueness of the imprinting mechanism (Q33885040) (← links)
- Discordance between genetic and epigenetic defects in pseudohypoparathyroidism type 1b revealed by inconsistent loss of maternal imprinting at GNAS1 (Q33905190) (← links)
- 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) (← links)
- Epigenetics and assisted reproductive technology: a call for investigation (Q33909693) (← links)
- Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome (Q33910416) (← links)
- Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome (Q33927299) (← links)
- RNA-directed DNA methylation. (Q34041209) (← links)
- Addition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yield. (Q34084829) (← links)
- Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes (Q34145399) (← links)
- Molecular genetics of Rett syndrome (Q34180570) (← links)
- Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer (Q34303935) (← links)
- Culture of oocytes and risk of imprinting defects. (Q34305206) (← links)
- KCNQ potassium channels: physiology, pathophysiology, and pharmacology (Q34305841) (← links)