About: Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans

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About: Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans Goto Sponge NotDistinct Permalink

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description	artículu científicu espublizáu en 1997 (ast) vědecký článek publikovaný v roce 1997 (cs) 1997 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована у вересні 1997 (uk) 1997 թվականի սեպտեմբերին հրատարակված գիտական հոդված (hy) 1997年學術文章 (zh) wetenschappelijk artikel (gepubliceerd op 1997/09/16) (nl) vedecký článok (publikovaný 1997/09/16) (sk) مقالة علمية (نشرت في 16-9-1997) (ar) article publié dans les Proceedings of the National Academy of Sciences of the United States of America (fr) scientific journal article (en) im September 1997 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28594559-ECBC697B-D1DD-411A-964D-622B5854798E
publication date	1997-09-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28594559-7C1DC0F5-E9F7-47C8-BA34-6BB49F32836E
language of work or name	English
cites work	wds:Q28594559-07BEA1C0-A96B-4288-AF43-9A8748208AF8 wds:Q28594559-0E72001A-3771-40EA-84F3-D7E140291FDC wds:Q28594559-11B0CC6D-CC68-47A1-ADEB-E49D4D58082B wds:Q28594559-15D9A461-B6BC-4ABA-8193-899E6B899952 wds:Q28594559-29567038-3523-484C-B3CE-BA81C8B7A4DD wds:Q28594559-2B1791B6-4C8D-4704-BECE-6211394E6F99 wds:Q28594559-2B260D2A-96BF-4AD2-A235-9C3811EC6962 wds:Q28594559-2CF94D56-A1F9-4A93-A50D-3A7174DF9D8C wds:Q28594559-2EE22617-D87E-4B1F-BF59-8B09A54C71BC wds:Q28594559-33543DF7-5EC0-4106-A8EA-963595B6A460 wds:Q28594559-48A32DB6-5108-41D6-A50A-CF4EF20412DE wds:Q28594559-4EB2FC06-22F4-48E2-85E1-3E462FE91262 wds:Q28594559-55233598-D034-4E99-8D9F-2BCCC5BC25FD wds:Q28594559-5C9E8DDB-9ECE-4094-BC5C-64061A7CC772 wds:Q28594559-5E08D7C6-7747-41C1-940C-87D7AB1A4116 wds:Q28594559-6563BC01-7F82-4E44-A5F2-5E72E0985CD9 wds:Q28594559-684A8E52-FC41-4636-AF2C-859BEDF1F6E6 wds:Q28594559-74203EE2-5D15-42E0-A01B-B09C12396F47 wds:Q28594559-930F2E66-BC87-42D8-8529-AAFFEA96A159 wds:Q28594559-9C279CE3-9766-42A0-9716-C6E1DFB219F8 wds:Q28594559-A59830D5-4005-4FFC-941D-20F53119146D wds:Q28594559-A7856C86-42B2-4011-8EAA-AE68C5B31FDC wds:Q28594559-B5708BD3-7F12-4695-9ECA-C6870D7BE1CB wds:Q28594559-BE50B283-8CF6-40EA-B4A4-9CB054EE96E9 wds:Q28594559-C40FB677-7AC8-48D6-832C-6E20AE8C2F14 wds:Q28594559-C4594D8E-483B-4E39-9101-65D7B9C7E7BC wds:Q28594559-C78C9DF5-4F82-4F08-9951-93036C929698 wds:Q28594559-CCD164D0-B74F-4A8E-9F45-1A78D36BF808 wds:Q28594559-D0793DA7-A6E6-4A61-A147-7AFD2821BBEB wds:Q28594559-D2F69E9B-6454-43A9-9A2E-83269FE5D00A wds:Q28594559-D9612B81-2060-4248-A343-74AD00C5BDFB wds:Q28594559-D9D28B11-CA81-41F4-8D05-D25225C21919 wds:Q28594559-EDE8B456-C2A3-4D1C-8923-D4F0B73D58C7 wds:Q28594559-FEFC5EAD-4849-47F7-9557-B4F4A348C08C
cites work	Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element A paternal-specific methylation imprint marks the alleles of the mouse H19 gene. A 5' differentially methylated sequence and the 3'-flanking region are necessary for H19 transgene imprinting Homologous association of oppositely imprinted chromosomal domains Parental imprinting of the mouse insulin-like growth factor II gene. Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain. Xist has properties of the X-chromosome inactivation centre The double-strand-break repair model for recombination Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis Completion of mouse embryogenesis requires both the maternal and paternal genomes Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour Epigenetic lesions at the H19 locus in Wilms' tumour patients Creation of genomic methylation patterns A modified and improved method for bisulphite based cytosine methylation analysis Gametic imprinting in mammals DNA demethylation in vitro: involvement of RNA. Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal. Interchromosomal Transfer of Epigenetic States in Ascobolus: Transfer of DNA Methylation Is Mechanistically Related to Homologous Recombination Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome Role for DNA methylation in genomic imprinting De novo DNA cytosine methyltransferase activities in mouse embryonic stem cells Disruption of imprinting caused by deletion of the H19 gene region in mice The inheritance of epigenetic defects The ontogeny of allele-specific methylation associated with imprinted genes in the mouse. The structural H19 gene is required for transgene imprinting Parental imprinting and human disease Evidence for intrachromosomal gene conversion in cultured mouse cells. Epigenetic mechanisms underlying the imprinting of the mouse H19 gene An enhancer deletion affects both H19 and Igf2 expression Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes. Multiple roles for DNA methylation in gametic imprinting Interchromosomal recombination is suppressed in mammalian somatic cells. Dynamic methylation adjustment and counting as part of imprinting mechanisms High-frequency germ line gene conversion in transgenic mice
author name string	wds:Q28594559-3690B95A-BF27-4A3F-B3DA-22CA2159A597 wds:Q28594559-978817FF-A434-41CE-854D-A7A008CD793A wds:Q28594559-9DFA5A6B-B60A-4A4E-9464-1FE8098DCE10 wds:Q28594559-AA875AC7-CF89-4B51-8D57-F4AD6FBD62E9 wds:Q28594559-ABF9D8F9-4C94-4EA6-990C-5D57DA6F8629 wds:Q28594559-DF5FFBD1-E304-47C7-BB64-FB34C0A2873D wds:Q28594559-E977B625-AB1B-4396-8488-9EF1110721B0
OpenCitations bibliographic resource ID	wds:Q28594559-7FB0FF22-4136-45CD-BEA6-E34F64C079B5
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/439179
author name string	T Forné S M Tilghman J Walter B Bailleul J Oswald L Dandolo

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