Interruption of intrachromosomal looping by CCCTC binding factor decoy proteins abrogates genomic imprinting of human insulin-like growth factor II.
about
A polycomb group protein is retained at specific sites on chromatin in mitosisRole of CTCF protein in regulating FMR1 locus transcriptionEffects of inhibition of hedgehog signaling on cell growth and migration of uveal melanoma cells.CRISPR Cas9-guided chromatin immunoprecipitation identifies miR483 as an epigenetic modulator of IGF2 imprinting in tumors.Regulation and Role of EZH2 in CancerA novel antisense long noncoding RNA within the IGF1R gene locus is imprinted in hematopoietic malignancies.Targeted gene suppression by inducing de novo DNA methylation in the gene promoter.Loss of maternal CTCF is associated with peri-implantation lethality of Ctcf null embryos.Epigenetic repression of RARRES1 is mediated by methylation of a proximal promoter and a loss of CTCF binding.Tissue-specific regulation of Igf2r/Airn imprinting during gastrulation.Hidden among the crowd: differential DNA methylation-expression correlations in cancer occur at important oncogenic pathwaysLong non-coding RNA ROR decoys gene-specific histone methylation to promote tumorigenesis.Antitumor potential of a synthetic interferon-alpha/PLGF-2 positive charge peptide hybrid molecule in pancreatic cancer cells.Promotion of the induction of cell pluripotency through metabolic remodeling by thyroid hormone triiodothyronine-activated PI3K/AKT signal pathwayA placental growth factor-positively charged peptide potentiates the antitumor activity of interferon-gamma in human brain glioblastoma U87 cellsGenomic imprinting and epigenetic control of developmentRegulation of the Human Telomerase Gene TERT by Telomere Position Effect-Over Long Distances (TPE-OLD): Implications for Aging and Cancer.Gene therapy for colorectal cancer by an oncolytic adenovirus that targets loss of the insulin-like growth factor 2 imprinting systemPromoter cross-talk via a shared enhancer explains paternally biased expression of Nctc1 at the Igf2/H19/Nctc1 imprinted locus.Loss of imprinting of IGF2 and the epigenetic progenitor model of cancerEpigenetic suppression of the antitumor cytotoxicity of NK cells by histone deacetylase inhibitor valproic acid.Association between birth weight and DNA methylation of IGF2, glucocorticoid receptor and repetitive elements LINE-1 and Alu.Long noncoding RNA-mediated intrachromosomal interactions promote imprinting at the Kcnq1 locus.Testis-specific transcriptional regulators selectively occupy BORIS-bound CTCF target regions in mouse male germ cells.Cohesin and related coiled-coil domain-containing complexes physically and functionally connect the dots across the genome.Long-range transcriptional regulation of breast cancer genes.Novel mutations in the RB1 gene from Chinese families with a history of retinoblastoma.An intragenic long noncoding RNA interacts epigenetically with the RUNX1 promoter and enhancer chromatin DNA in hematopoietic malignancies.Epigenetic reprogramming reverses the malignant epigenotype of the MMP/TIMP axis genes in tumor cells.Promoter histone H3K27 methylation in the control of IGF2 imprinting in human tumor cell linesInduced DNA demethylation can reshape chromatin topology at the IGF2-H19 locus.Converting Skin Fibroblasts into Hepatic-like Cells by Transient Programming.Epigenomics and targeted therapy in cancer.Discovering a binary CTCF code with a little help from BORIS.Increased In Vitro Osteopotential in SHED Associated with Higher IGF2 Expression When Compared with hASCs.Simultaneous hyper- and hypomethylation at imprinted loci in a subset of patients with GNAS epimutations underlies a complex and different mechanism of multilocus methylation defect in pseudohypoparathyroidism type 1b.Graphene oxide regulates cox2 in human embryonic kidney 293T cells via epigenetic mechanisms: dynamic chromosomal interactions.Disruption of Chromosomal Architecture of cox2 Locus Sensitizes Lung Cancer Cells to RadiotherapyExtensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome
P2860
Q28484449-0755A9E7-079F-43D9-BB86-6268A0CCAC9BQ28534708-6087B038-3B1D-4B31-B64F-CD780811E586Q33631459-2B4F5B76-7E60-4460-A0D2-4060D8E9B36AQ33798311-7C99BC92-E12E-416E-9E76-78F6A9AAA8FAQ34043370-D093B20E-EF54-402A-BE4E-D681124B953AQ34115325-188B723B-6491-485C-B9DC-C3330A4935D3Q34115881-D81B47A7-3A77-4E25-AB46-39513FD086BEQ34245001-E65C9E7D-5848-4C5F-8EFC-22FAA2ED2A9FQ34277489-17628666-C0A7-4C04-86C0-4943575FAFDCQ35540610-5FDB22BC-216A-48D2-80F9-B61B9C2D59FAQ35600057-27FD4BE7-17A0-4B30-85EC-E3345CA1F118Q35844784-8ACC8DF4-B9F5-4649-932F-48D29A0E8423Q35846233-8278FD9F-876E-4CCA-8EFF-37298969B370Q35981059-F7429F6D-A5B6-4239-80E7-656BF00071D3Q36019591-E6083206-CCEE-4219-8DD7-6D8F6F919882Q36065882-7AE94465-4AB7-4A8F-90ED-E18F0A06B033Q36224732-DA800F42-BAB8-4D4C-8588-22105C1D3E9FQ36538951-48E2DF8F-58DD-4CC0-A572-7EECF3F9B73BQ36559183-52E41D65-31F1-4157-AB05-1BB9884B1F2FQ36813932-4927E630-396D-42C2-967F-4B9205C80550Q36853857-75FCCD74-A127-41CA-BEC1-B6C632ECFD13Q37209067-529F9244-0A35-4F5B-B671-33077821F6C4Q37441308-EA1F4BBA-EB9F-44AC-B683-6D0DCB2AE8B2Q37618285-6353F2E3-8B57-459C-B534-2294A8A3D9CFQ37912942-D5EE38FF-393E-46EF-8B69-956F9464A31DQ38053130-39B457BF-E456-4D89-BBA5-4CB89EB8C995Q38937782-7D21B696-2DBA-4A8B-85AA-90FA331EA62BQ39002254-20EF3213-2DB4-4383-BDA6-472A50554B5DQ39084351-4AFEBAB0-54B4-472E-94B8-A057517B5F11Q39107608-EDB810D5-4F2D-495A-8439-F987226B2F70Q39166609-E06B88E0-1779-4FA1-8646-BC31F546B096Q41030569-07048D7F-F69C-4AF9-B1DC-36CE2969DA1CQ46117582-8CC1C151-4158-47ED-B416-1BA7B3247996Q48114058-1EE30FCE-37B0-4FA4-9E16-BA54A89A1210Q50982222-C60E442E-2B8D-47DD-8D40-D2FDB58CD65CQ51014930-4D873798-19B8-486D-8C95-44378256BA05Q52394135-7790AFED-2C67-4949-9F1E-6730A59845A2Q57039796-365F03AD-4445-4F00-937E-B2B891824AC4Q57199288-8DA48FB9-31AE-421D-BA51-F582EB62BF93
P2860
Interruption of intrachromosomal looping by CCCTC binding factor decoy proteins abrogates genomic imprinting of human insulin-like growth factor II.
description
2011 nî lūn-bûn
@nan
2011 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Interruption of intrachromosom ...... insulin-like growth factor II.
@ast
Interruption of intrachromosom ...... insulin-like growth factor II.
@en
Interruption of intrachromosom ...... insulin-like growth factor II.
@nl
type
label
Interruption of intrachromosom ...... insulin-like growth factor II.
@ast
Interruption of intrachromosom ...... insulin-like growth factor II.
@en
Interruption of intrachromosom ...... insulin-like growth factor II.
@nl
prefLabel
Interruption of intrachromosom ...... insulin-like growth factor II.
@ast
Interruption of intrachromosom ...... insulin-like growth factor II.
@en
Interruption of intrachromosom ...... insulin-like growth factor II.
@nl
P2093
P2860
P356
P1476
Interruption of intrachromosom ...... insulin-like growth factor II
@en
P2093
Andrew R Hoffman
Beibei Niu
Brandon N Steelman
Guanxiang Qian
Haibo Wang
Jianqun Ling
Shengfang Ge
P2860
P304
P356
10.1083/JCB.201101021
P407
P50
P577
2011-05-01T00:00:00Z