about
Large-scale identification of human genes implicated in epidermal barrier functionTumor transcriptome sequencing reveals allelic expression imbalances associated with copy number alterationsDifferential gene expression in tumorigenic and nontumorigenic HeLa x normal human fibroblast hybrid cellsMaternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndromeThe imprinted H19 gene is a marker of early recurrence in human bladder carcinoma.The product of the imprinted H19 gene is an oncofetal RNAGenomic imprinting disorders in humans: a mini-reviewH19 overexpression in breast adenocarcinoma stromal cells is associated with tumor values and steroid receptor status but independent of p53 and Ki-67 expressionComputational and experimental identification of novel human imprinted genesLong Non-coding RNAs in the CytoplasmLncRNAs in Stem CellsThe origin and evolution of genomic imprinting and viviparity in mammalsCurrent Status of Long Non-Coding RNAs in Human Breast CancerTwo novel genes in the center of the 11p15 imprinted domain escape genomic imprintingImprinted H19 gene expression in embryogenesis and human cancer: the oncofetal connectionParental imprinting of the human H19 geneThioredoxin post-transcriptional regulation by H19 provides a new function to mRNA-like non-coding RNASmall nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical regionThe expression of the imprinted H19 and IGF-2 genes in human bladder carcinomaThe H19 long noncoding RNA gives rise to microRNAs miR-675-3p and miR-675-5p to promote skeletal muscle differentiation and regeneration.Gtx: a novel murine homeobox-containing gene, expressed specifically in glial cells of the brain and germ cells of testis, has a transcriptional repressor activity in vitro for a serum-inducible promoterPhysical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2.Genomic imprinting: implications for human disease.Mapping allele-specific DNA methylation: a new tool for maximizing information from GWAS.The French Wilms' tumour study: no clear evidence for cancer prone families.Parental origin of transcription from the human GNAS1 gene.Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndromeLncRNA H19 promotes the differentiation of bovine skeletal muscle satellite cells by suppressing Sirt1/FoxO1.Imprinted genes as potential genetic and epigenetic toxicologic targetsGenetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways.Inter- and intra-individual variation in allele-specific DNA methylation and gene expression in children conceived using assisted reproductive technology.Wilms tumor genetics.The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblasts.Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor.Lentivirus-mediated RNA interference targeting the H19 gene inhibits cell proliferation and apoptosis in human choriocarcinoma cell line JARDisruption of imprinted genes at chromosome region 11p15.5 in paediatric rhabdomyosarcomaAltered DNA methylation patterns of the H19 differentially methylated region and the DAZL gene promoter are associated with defective human sperm.Assessment of genomic imprinting of SLC38A4, NNAT, NAP1L5, and H19 in cattleA radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci
P2860
Q21092869-43D98BA7-475D-45A7-AA49-E35285413E4AQ21562666-4E266DD4-B146-46F6-9527-2BEABBD427DFQ22010820-62C80082-7760-4D21-8E14-A53240B0A98BQ24305283-1B55BDF1-3BBB-40F7-A929-4DD1CA4E86B5Q24535316-43275FBC-AC9A-4FE8-BD95-F3A7115AAF09Q24609254-4A2349D2-E20D-4094-A2C6-A090BBD28D36Q24646016-C4BCA2ED-2209-4676-BDCA-F2350D7BC3FFQ24682023-A79F23BE-028B-4CCF-8AD3-9A92CBA43F26Q24684684-0166144D-FB4D-49D0-BA88-8DDD69CD6A43Q26750883-C2368F9C-459D-46D0-B4D6-B4E485BDC3A7Q26765910-D667359C-7CBB-478C-9581-821336E27587Q27007861-3A9914AF-79D1-47A1-92B6-F9482A7797E8Q28079880-0041325C-0EA0-4DB5-A336-53526832F7C3Q28138506-0424FF6B-C410-4CB2-8667-ED80A8116A8CQ28140949-2F753C4E-A2B7-4DCF-B3A3-75B42F00E87AQ28187996-9FCD2026-2FBF-411A-961A-F400D7F91E31Q28207541-5A92A7BA-FDEE-42B8-A1DD-D6AF8D15691EQ28208127-9B7E52A0-4F45-4CEC-90E6-5B0FD2928D25Q28291512-4F8FDC92-3D50-4E8F-83D9-EC94D874B343Q28505070-A9FAE5CA-6E1F-4380-A93D-326DAA1FF7E5Q28505457-F0482895-B32F-40C9-A00D-AF5B71193D83Q31158518-701E8EA8-5B4E-4588-B11D-66E4F862B142Q33541538-487E7BC7-2A0A-4C95-8467-D6B7BAF69B7BQ33645971-103DA50E-E410-42C1-BDF6-2D0AAEC46DFFQ33674308-AF55B9A9-8CFE-4785-AB73-640677B34320Q33674736-885D4EE6-DE2F-4B29-A489-410B119A4A52Q33675226-18F66CCD-AEAE-4BDB-820C-8C687375FAF7Q33679562-8914F696-2383-4C8E-AEF1-8738B20B4C63Q33827281-A8B38E52-490D-4852-93F6-8AA9B9017F6EQ33852775-18864991-AB50-45DA-AB26-0D5A1A207EB5Q33875930-6BA5C0B7-3237-454B-AC51-F2BCF4BFC746Q34014319-AF40C7C3-5D59-40BA-875D-9DABCB14FB39Q34067724-82AC899E-578D-43C7-888B-D09E51CE7F60Q34428055-76E359C0-38FB-4415-B497-6D515ADA4CDDQ34572727-F729612B-0C6E-4EE4-B6F5-E1300D36630CQ34742149-52BB5D11-0B53-4D18-BBEE-78B27039C756Q34786119-93BAB1D5-95E5-487E-8BB7-3230FE6B3CE9Q34981288-23D75760-EBAC-40DD-B300-6D2393C9D974Q35118908-F29EBF11-839E-4734-870A-A9F6A4FD4298Q35194082-3D0CD8D0-5F4C-4A32-A23A-665FCADEA238
P2860
description
1992 nî lūn-bûn
@nan
1992 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Monoallelic expression of the human H19 gene
@ast
Monoallelic expression of the human H19 gene
@en
Monoallelic expression of the human H19 gene
@nl
type
label
Monoallelic expression of the human H19 gene
@ast
Monoallelic expression of the human H19 gene
@en
Monoallelic expression of the human H19 gene
@nl
prefLabel
Monoallelic expression of the human H19 gene
@ast
Monoallelic expression of the human H19 gene
@en
Monoallelic expression of the human H19 gene
@nl
P2860
P3181
P356
P1433
P1476
Monoallelic expression of the human H19 gene
@en
P2860
P2888
P3181
P356
10.1038/NG0492-40
P407
P577
1992-04-01T00:00:00Z