Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans
about
A family of human zinc finger proteins that bind methylated DNA and repress transcriptionMaternal disruption of Ube3a leads to increased expression of Ube3a-ATS in trans.Long noncoding RNAs as novel predictors of survival in human cancer: a systematic review and meta-analysisNoncoding RNAs, Emerging Regulators of Skeletal Muscle Development and DiseasesPairing of homologous regions in the mouse genome is associated with transcription but not imprinting statusA non-coding RNA within the Rasgrf1 locus in mouse is imprinted and regulated by its homologous chromosome in transTransvection effects involving DNA methylation during meiosis in the mouse.Closely related proteins MBD2 and MBD3 play distinctive but interacting roles in mouse developmentAn upstream repressor element plays a role in Igf2 imprintingA point mutation in bioactive RNA results in the failure of mutant heart correction in Mexican axolotls.Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7.Evf2 (Dlx6as) lncRNA regulates ultraconserved enhancer methylation and the differential transcriptional control of adjacent genes.An intragenic methylated region in the imprinted Igf2 gene augments transcription.H19 lncRNA controls gene expression of the Imprinted Gene Network by recruiting MBD1.Analysis of sequence upstream of the endogenous H19 gene reveals elements both essential and dispensable for imprintingDNA methylation and mammalian epigenetics.Different epigenetic alterations are associated with abnormal IGF2/Igf2 upregulation in neural tube defects.An analysis of transvection at the yellow locus of Drosophila melanogaster.Genomic imprinting controls matrix attachment regions in the Igf2 geneLong-range chromatin interactions at the mouse Igf2/H19 locus reveal a novel paternally expressed long non-coding RNA.Igf2 imprinting does not require its own DNA methylation or H19 RNA.Stem cell activation in skeletal muscle regeneration.Clonal heterogeneity at allelic methylation sites diagnostic for Prader-Willi and Angelman syndromes.The nucleotides responsible for the direct physical contact between the chromatin insulator protein CTCF and the H19 imprinting control region manifest parent of origin-specific long-distance insulation and methylation-free domainsChromosome loops, insulators, and histone methylation: new insights into regulation of imprinting in clusters.Enhancer competition between H19 and Igf2 does not mediate their imprinting.Mapping Human Pluripotent-to-Cardiomyocyte Differentiation: Methylomes, Transcriptomes, and Exon DNA Methylation "Memories".Transvection mediated by the translocated cyclin D1 locus in mantle cell lymphoma.A novel H19 antisense RNA overexpressed in breast cancer contributes to paternal IGF2 expressionTrans allele methylation and paramutation-like effects in mice.Widespread recovery of methylation at gametic imprints in hypomethylated mouse stem cells following rescue with DNMT3A2.ESR1 gene promoter region methylation in free circulating DNA and its correlation with estrogen receptor protein expression in tumor tissue in breast cancer patients.Long noncoding RNAs, emerging players in muscle differentiation and disease.Evolution of the Beckwith-Wiedemann syndrome region in vertebrates.Loss of Igf2 imprinting in monoclonal mouse hepatic tumor cells is not associated with abnormal methylation patterns for the H19, Igf2, and Kvlqt1 differentially methylated regions.Exposure of mouse preimplantation embryos to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) alters the methylation status of imprinted genes H19 and Igf2.Role of Non-Coding RNAs in the Etiology of Bladder Cancer.Chromatin-associated noncoding RNAs in development and inheritance.Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human.Deletion of the ANKRD15 gene at 9p24.3 causes parent-of-origin-dependent inheritance of familial cerebral palsy.
P2860
Q24298802-4BA716FB-EE8C-45A0-92A1-62C18131DAD9Q24531844-53C3359A-4CB7-4E5E-AAC7-187F6A3D6B9BQ26746258-EFB1B44A-383D-4EF5-842E-5E73A6AE90F2Q26799919-C60CF2E9-4AF2-4476-87E2-401E44964C3FQ27301083-0F77C7F8-45BC-414D-9B03-36AD846B5E80Q27317100-6FC23F2C-FF8A-46FE-915B-445A6F5A9FD2Q28217139-5B8E0EDA-ED96-480E-92B7-A724159E7C81Q28584750-6F75421D-51B5-43A0-BB24-6E9BFE6E9F90Q30684867-0D04BF42-369B-4E74-BFD9-636C9E9A135AQ30921996-73A70230-F3A3-41D3-9324-03ED8850E80DQ33285306-2B1826EE-2C11-40D2-BEE4-6F33521E4F8CQ33557441-C006C8BB-8C35-4350-AE72-A94067CC3736Q33757992-1A4C58E6-E131-4CBA-9E4F-61BCAB67296AQ34039202-6840D2DF-84EF-4463-B7C6-847D04FD5F6BQ34277546-5FCF9CC2-EC7B-4008-AFF1-7FDCEFCA804EQ34375355-B002B456-8288-47C6-AD78-67D3BF5E2657Q34572114-5A6C8C2D-599B-4CA2-9F8C-4093ED894BA9Q34606309-35C5287D-B66C-4521-89FC-22D8F20E4F42Q34986939-ADEE23A7-85D5-4A31-87E5-C14F35C90E55Q35153510-AC3F74FF-C7C3-4F29-BC89-A1DE0B45C601Q35205921-AF7EA7A8-C0B1-4494-81D7-165BA8A25DCEQ35547307-85EB852A-F02C-4CA5-98D2-A6FC0430A3B4Q35881189-C8950137-3B12-474B-9837-8DF402DE0735Q35964289-9947AB7F-1820-42C1-88DC-A4D5C8D821FDQ36238491-C7B388AA-5A5D-482A-97EC-04961AE7BBB7Q36430736-D18A86CF-274B-494A-A25D-1EA408176DB6Q36645680-F60966EE-B169-4BC4-892F-61470312FD97Q36851904-FA455AB8-DF8C-4BF1-93C2-FFDF3A6F9436Q36949891-90CA9A59-9A1B-4A25-A10D-87A530C242F3Q37347022-4969CDC6-ECD7-44BD-8017-0BC181386302Q37428393-A4CBD1FC-F6ED-42C7-ACAA-00646E9C48E5Q37580662-25B794BF-31BE-4977-BC13-AF5CEC867F12Q37680875-B7B72719-500E-407A-9F73-0216EC7B3B65Q40774859-06F359D3-AF45-467F-A134-B90392368469Q44244884-E718042F-2884-49CA-A33D-E3A1BF0E103FQ44762564-0CB23808-7B04-4BAB-A12D-10CDBFBC9072Q46236214-0770EDDD-39E4-4476-B111-EDF6C6DF2640Q46316443-63EE6CC1-E584-4418-8A59-E811C3C6D67CQ48096674-4266B087-763D-4ACD-8372-DD1BF8887428Q51831412-4FC52A05-A1CB-48E1-9FB1-FFA0ACE8BEF7
P2860
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans
description
1997 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
article publié dans les Procee ...... f the United States of America
@fr
artículu científicu espublizáu en 1997
@ast
im September 1997 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1997/09/16)
@sk
vědecký článek publikovaný v roce 1997
@cs
wetenschappelijk artikel (gepubliceerd op 1997/09/16)
@nl
наукова стаття, опублікована у вересні 1997
@uk
name
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans
@ast
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans
@en
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans
@nl
type
label
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans
@ast
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans
@en
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans
@nl
prefLabel
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans
@ast
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans
@en
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans
@nl
P2093
P2860
P3181
P356
P1476
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans
@en
P2093
B Bailleul
S M Tilghman
P2860
P304
10243-10248
P3181
P356
10.1073/PNAS.94.19.10243
P407
P577
1997-09-01T00:00:00Z