Disruption of imprinting caused by deletion of the H19 gene region in mice
about
A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical regionBirth of parthenogenetic mice that can develop to adulthoodPlacental overgrowth in mice lacking the imprinted gene IplElongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genesTranslational and structural requirements of the early nodulin gene enod40, a short-open reading frame-containing RNA, for elicitation of a cell-specific growth response in the alfalfa root cortexTissue-specific and imprinted epigenetic modifications of the human NDN geneEnod40, a short open reading frame-containing mRNA, induces cytoplasmic localization of a nuclear RNA binding protein in Medicago truncatulaDwarfism and impaired gut development in insulin-like growth factor II mRNA-binding protein 1-deficient miceImprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15The product of the imprinted H19 gene is an oncofetal RNAHigh-resolution analysis of parent-of-origin allelic expression in the mouse brainThe H19 lincRNA is a developmental reservoir of miR-675 that suppresses growth and Igf1rA maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndromeGene structure, DNA methylation, and imprinted expression of the human SNRPN geneSilencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndromeTranscriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samplesAnalysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationH19 overexpression in breast adenocarcinoma stromal cells is associated with tumor values and steroid receptor status but independent of p53 and Ki-67 expressionLoss 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 imprintingImprinting: silently crossing the boundary.Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humansLong non-coding RNA-mediated regulation of glucose homeostasis and diabetesMechanisms of long noncoding RNA function in development and diseaseGenomic imprinting effects on complex traits in domesticated animal speciesThe role of placental nutrient sensing in maternal-fetal resource allocationTranscriptome complexity in cardiac development and diseases--an expanding universe between genome and phenomeDiverse Phenotypes and Specific Transcription Patterns in Twenty Mouse Lines with Ablated LincRNAsThe role and interaction of imprinted genes in human fetal growthGlypican-3-deficient mice exhibit developmental overgrowth and some of the abnormalities typical of Simpson-Golabi-Behmel syndromeH19 RNA binds four molecules of insulin-like growth factor II mRNA-binding proteinImprinted H19 gene expression in embryogenesis and human cancer: the oncofetal connectionCTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locusFrequent loss of imprinting of IGF2 and MEST in lung adenocarcinomaTargeted knockdown of the RNA-binding protein CRD-BP promotes cell proliferation via an insulin-like growth factor II-dependent pathway in human K562 leukemia cellsThe H19 long noncoding RNA gives rise to microRNAs miR-675-3p and miR-675-5p to promote skeletal muscle differentiation and regeneration.FoxA proteins regulate H19 endoderm enhancer E1 and exhibit developmental changes in enhancer binding in vivoThe H19 locus acts in vivo as a tumor suppressorRole of CTCF binding sites in the Igf2/H19 imprinting control regionAlcohol Regulates Genes that Are Associated with Response to Endocrine Therapy and Attenuates the Actions of Tamoxifen in Breast Cancer CellsCTCF maintains differential methylation at the Igf2/H19 locus
P2860
Q22009166-405326DA-B71C-4E83-8061-D43C1D35DE03Q22122493-4EA41ED8-C04D-44A5-ADCA-BCFFE1B95F8FQ24530568-AC480E59-D8F7-4094-AB39-2DD3B13AE47CQ24546155-8294FACC-ABF5-4586-B8B2-EC881CD6394BQ24550749-434BAAE7-0C3D-4AD2-A1FD-AF5959E84054Q24564544-47631A0C-C794-43E1-8198-88C708A68850Q24564884-8B4A47E6-2911-444F-9E06-D276C5237E4DQ24567609-A85D1407-5082-412C-B339-0E75DDD3D3C0Q24568014-DF0E579B-5DEA-40A4-8A3B-97A5D798E4B9Q24609254-0EC3BDF4-6558-4692-86E6-25C9DB7246A9Q24626579-9BD1A44A-346C-48CC-957F-551293E660C4Q24633774-68AB773F-1F98-4D7A-9026-CFFC3BA84BBEQ24644175-84217AEB-F8B7-4439-9703-F01220C31381Q24676443-0D520391-7D4D-466A-BF23-516DD164FA27Q24678326-F2358788-F2C4-4204-B6AD-C7990B23D303Q24681580-A324674D-021D-45EB-9A56-EA9C181CD623Q24681734-65A838A7-35FD-4741-9B9C-7E26939B0179Q24682023-A2265E41-B324-4AE5-9E18-2A5444BF14D3Q24684284-93181719-9758-43E7-AB44-924E5886FDFFQ24804906-4DF23495-18F7-4034-94F9-8951AA554CC0Q24810018-A4BA6660-BD9C-41B6-8DA3-3B582AD0382CQ26747596-D61C8AF7-D029-47F6-8DD7-040BE5ACE275Q26752329-8031FCF7-0F53-481F-BFB8-F9B997FA227FQ26824384-3B7BB315-6CA9-4444-B25B-228973E28140Q27008068-66179530-5CE0-42FF-A1F0-BC17C0BECB5EQ27027884-AB101B76-3C7A-4105-8763-B36124F94785Q27308418-EC689958-D1A6-42BC-A5C0-D89B5B3A3F08Q28083223-851E021A-74E7-43A8-9CEA-5A50EBFB92B6Q28139404-50347325-FBB4-403F-8D4A-CADC475685FFQ28139674-5E286FBA-FA2A-466D-9F54-98094DC6D4A8Q28140949-EAE01D14-7EA7-457C-8BB5-7DB60AE0EBEEQ28145756-708734DB-08C4-4CF8-B06A-0564A4E6BC67Q28215251-BCFD93DA-7C1A-4C7D-BB31-B560B0F1CDAAQ28281008-318109EA-ADA6-4862-A37E-939A01E98464Q28505070-BFE58DFC-7FE1-4D20-9EBA-0728E147439EQ28505087-A974E62F-9FC2-4143-ACBA-D90B56B814FAQ28508794-DEE13540-BBC6-48EF-9243-534A1458718CQ28512182-E4F7246F-DB61-498C-BC1B-09378015FC23Q28551506-81724C46-9859-4324-89F3-113D2F314648Q28593901-43139299-1689-432F-A7D6-2369914EA6AD
P2860
Disruption of imprinting caused by deletion of the H19 gene region in mice
description
1995 nî lūn-bûn
@nan
1995 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Disruption of imprinting caused by deletion of the H19 gene region in mice
@ast
Disruption of imprinting caused by deletion of the H19 gene region in mice
@en
Disruption of imprinting caused by deletion of the H19 gene region in mice
@nl
type
label
Disruption of imprinting caused by deletion of the H19 gene region in mice
@ast
Disruption of imprinting caused by deletion of the H19 gene region in mice
@en
Disruption of imprinting caused by deletion of the H19 gene region in mice
@nl
prefLabel
Disruption of imprinting caused by deletion of the H19 gene region in mice
@ast
Disruption of imprinting caused by deletion of the H19 gene region in mice
@en
Disruption of imprinting caused by deletion of the H19 gene region in mice
@nl
P2093
P3181
P356
P1433
P1476
Disruption of imprinting caused by deletion of the H19 gene region in mice
@en
P2093
A Efstratiadis
J Eggenschwiler
P A Leighton
R S Ingram
S M Tilghman
P2888
P3181
P356
10.1038/375034A0
P407
P577
1995-05-04T00:00:00Z
P6179
1052910955