Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.
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Insulin-like growth factors promote vasculogenesis in embryonic stem cellsA family of insulin-like growth factor II mRNA-binding proteins represses translation in late developmentDisruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndromePlacental overgrowth in mice lacking the imprinted gene IplLin28a transgenic mice manifest size and puberty phenotypes identified in human genetic association studiesSilencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndromeAnalysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationLoss 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 imprintingmicroRNAs as Potential Biomarkers in Adrenocortical Cancer: Progress and ChallengesThe origin and evolution of genomic imprinting and viviparity in mammalsAnalysis of the role of Igf2 in adrenal tumour development in transgenic mouse modelsGlypican-3-deficient mice exhibit developmental overgrowth and some of the abnormalities typical of Simpson-Golabi-Behmel syndromeTargeted knockdown of the RNA-binding protein CRD-BP promotes cell proliferation via an insulin-like growth factor II-dependent pathway in human K562 leukemia cellsA domesticated transposon mediates the effects of a single-nucleotide polymorphism responsible for enhanced muscle growthGenomic imprinting: implications for human disease.Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome.Turnover of primary transcripts is a major step in the regulation of mouse H19 gene expressionMultiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster.Beckwith-Wiedemann syndrome: imprinting in clusters revisited.Imprinted genes as potential genetic and epigenetic toxicologic targetsEpigenetics and assisted reproductive technology: a call for investigation.Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor.Telomeric NAP1L4 and OSBPL5 of the KCNQ1 cluster, and the DECORIN gene are not imprinted in human trophoblast stem cells.Epigenetic regulatory mechanisms associated with infertilityRelaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes.Differential differences in methylation status of putative imprinted genes among cloned swine genomes.All in the family: the BTB/POZ, KRAB, and SCAN domainsEpigenetic silencing of beta-spectrin, a TGF-beta signaling/scaffolding protein in a human cancer stem cell disorder: Beckwith-Wiedemann syndrome.A genomic imprinting defect in mice traced to a single geneChest wall hamartoma with Wiedemann-Beckwith syndrome: clinical report and brief review of chromosome 11p15.5-related tumors.Cytosine methylation and the unequal developmental potentials of the oocyte and sperm genomesThe role of genomic imprinting in biology and disease: an expanding view.Dietary supplementation with polyunsaturated fatty acid during pregnancy modulates DNA methylation at IGF2/H19 imprinted genes and growth of infants.Relationship of folate, vitamin B12 and methylation of insulin-like growth factor-II in maternal and cord bloodDisruption of imprinted genes at chromosome region 11p15.5 in paediatric rhabdomyosarcomamTOR phosphorylates IMP2 to promote IGF2 mRNA translation by internal ribosomal entryRegulation of supply and demand for maternal nutrients in mammals by imprinted genes.Autoantibodies to tumor-associated antigens as biomarkers in cancer immunodiagnosis.Genome-wide analysis of DNA methylation in bovine placentas
P2860
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P2860
Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh
1997年學術文章
@zh-hant
name
Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.
@en
type
label
Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.
@en
prefLabel
Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.
@en
P50
P356
P1433
P1476
Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome
@en
P2093
P2888
P304
P356
10.1038/39797
P407
P577
1997-10-01T00:00:00Z
P6179
1029474313