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KCNQ1OT1
Nucleoporin 107, 62 and 153 Mediate Kcnq1ot1 Imprinted Domain Regulation in Extraembryonic Endoderm Stem Cells
Functional Classification of Long Non-Coding Rnas by K-Mer Content
Depletion of Kcnq1ot1 Non-Coding RNA Does Not Affect Imprinting Maintenance in Stem Cells Michael C
Wilms Tumour in Beckwith–Wiedemann Syndrome and Loss of Methylation at Imprinting Centre 2: Revisiting Tumour Surveillance Guidelines
Two Maternal Duplications Involving the CDKN1C Gene Are Associated
Expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 and The
The Long Noncoding RNA Kcnq1ot1 Organises a Lineage- Specific Nuclear Domain for Epigenetic Gene Silencing Lisa Redrup1, Miguel R
Identi Cation of Novel Hub Genes Through Expression Pro Les
Kcnq1ot1/Lit1 Noncoding RNA Mediates Transcriptional Silencing
Disruption of KCNQ1 Prevents Methylation of the ICR2 and Supports the Hypothesis That Its Transcription Is Necessary for Imprint Establishment
Origins of DNA Methylation Defects in Wilms Tumors
Construction and Analysis of a Lncrna‑Mirna‑Mrna Network Based on Competitive Endogenous RNA Reveals Functional Lncrnas in Diabetic Cardiomyopathy
Elongation of the Kcnq1ot1 Transcript Is Required for Genomic Imprinting of Neighboring Genes
Association Study Between KCNQ1 and KCNQ1OT1 Genetic Polymorphisms and Gastric Cancer Susceptibility and Survival in a Chinese Han Population: a Case-Control Study
View of Parkinson’S Disease
Paternal Allelic Mutation at the Kcnq1 Locus Reduces Pancreatic Β-Cell Mass by Epigenetic Modification of Cdkn1c
Beckwith-Wiedemann Syndrome
Paternal Allelic Mutation at the Kcnq1 Locus Reduces Pancreatic Β-Cell Mass by Epigenetic Modification of Cdkn1c
Top View
Growth Regulation, Imprinted Genes, and Chromosome 11P15.5
Controversies and Advances in the Management of Wilms' Tumour
Genetic Variation Affecting DNA Methylation and the Human
Pyrrole-Imidazole Polyamide-Mediated Silencing of KCNQ1OT1 Expression Induces Cell Death in Wilms' Tumor Cells
KCNQ1OT1 Gene KCNQ1 Opposite Strand/Antisense Transcript 1
The Effectiveness of Wilms Tumor Screening in Beckwith–Wiedemann Spectrum
Wiedemann Syndrome and Related Disorders
Looking for CDKN1C Enhancers
Sequence Variants Identification at the KCNQ1OT1:TSS Differentially
Characterization of Global Loss of Imprinting in Fetal Overgrowth Syndrome Induced by Assisted Reproduction
Imprinting Mechanisms—It Only Takes Two
Hypomethylation of the KCNQ1OT1 Imprinting Center of Chromosome 11 Associated to Sotos-Like Features
Human Long Noncoding RNA Interactome: Detection, Characterization and Function
Long Non-Coding RNA KCNQ1 Opposite Transcript 1 (KCNQ1OT1
Characterization of the Mouse KCNQ1OT1 Noncoding RNA
Lncrna KCNQ1OT1 Activated by C-Myc Promotes Cell Proliferation Via Interacting with FUS to Stabilize MAP3K1 in Acute Promyelocytic Leukemia
Disruption of KCNQ1 Prevents Methylation of the ICR2 and Supports the Hypothesis That Its Transcription Is Necessary for Imprint Establishment
The Biological Roles of Lncrnas and Future Prospects in Clinical Application