Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes - Wikidata - awgldk - TriplyDB

Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes

Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes

http://www.wikidata.org/entity/Q35197831

about

Periconceptional maternal folic acid use of 400 microg per day is related to increased methylation of the IGF2 gene in the very young child A family of insulin-like growth factor II mRNA-binding proteins represses translation in late development Interchromosomal associations between alternatively expressed loci Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome Placental overgrowth in mice lacking the imprinted gene Ipl Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome Analysis of the role of Igf2 in adrenal tumour development in transgenic mouse models Glypican-3-deficient mice exhibit developmental overgrowth and some of the abnormalities typical of Simpson-Golabi-Behmel syndrome H19 RNA binds four molecules of insulin-like growth factor II mRNA-binding protein IMP3 is a novel biomarker for adenocarcinoma in situ of the uterine cervix: an immunohistochemical study in comparison with p16(INK4a) expression Hectd1 is required for development of the junctional zone of the placenta Effects of mutations in the insulin-like growth factor signaling system on embryonic pancreas development and beta-cell compensation to insulin resistance A 14-kDa cathepsin L-derived carboxyl IGFBP-2 fragment is sequestered by cultured rat ileal crypt cells Genes responsive to low-intensity pulsed ultrasound in MC3T3-E1 preosteoblast cells.Neurodevelopmental effects of insulin-like growth factor signaling.In silico regulatory analysis for exploring human disease progression.Proline-rich tyrosine kinase 2 (Pyk2) regulates IGF-I-induced cell motility and invasion of urothelial carcinoma cells.Assisted Reproductive Technology affects developmental kinetics, H19 Imprinting Control Region methylation and H19 gene expression in individual mouse embryos.Postnatal survival of mice with maternal duplication of distal chromosome 7 induced by a Igf2/H19 imprinting control region lacking insulator function Decorin differentially modulates the activity of insulin receptor isoform A ligands.Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster.Genetic analysis of Hedgehog signaling in ventral body wall development and the onset of omphalocele formation.Beckwith-Wiedemann syndrome: imprinting in clusters revisited.Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways.The insulin-like growth factor receptor I promotes motility and invasion of bladder cancer cells through Akt- and mitogen-activated protein kinase-dependent activation of paxillin.Analysis of the dynamics of limb transcriptomes during mouse development.Monotreme IGF2 expression and ancestral origin of genomic imprinting.Relaxation 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.Adaptation of nutrient supply to fetal demand in the mouse involves interaction between the Igf2 gene and placental transporter systems.Epigenetic 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 gene Glypicans: proteoglycans with a surprise.Cloning in reproductive medicine.Large offspring syndrome and other consequences of ruminant embryo culture in vitro: relevance to blastocyst culture in human ART.Genetic disorders of human growth.Ligand-mediated endocytosis and trafficking of the insulin-like growth factor receptor I and insulin receptor modulate receptor function.IGF signaling directs ventricular cardiomyocyte proliferation during embryonic heart development.Activin induces x-zone apoptosis that inhibits luteinizing hormone-dependent adrenocortical tumor formation in inhibin-deficient mice.Regulation of supply and demand for maternal nutrients in mammals by imprinted genes.Autoantibodies to tumor-associated antigens as biomarkers in cancer immunodiagnosis.

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Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes

http://www.wikidata.org/entity/Q35197831

description

1997 nî lūn-bûn

@nan

1997 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1997 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

1997年の論文

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1997年論文

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1997年論文

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1997年論文

@zh-hk

1997年論文

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1997年論文

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1997年论文

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name

Mouse mutant embryos overexpre ...... impson-Golabi-Behmel syndromes

@ast

Mouse mutant embryos overexpre ...... impson-Golabi-Behmel syndromes

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type

label

Mouse mutant embryos overexpre ...... impson-Golabi-Behmel syndromes

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Mouse mutant embryos overexpre ...... impson-Golabi-Behmel syndromes

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prefLabel

Mouse mutant embryos overexpre ...... impson-Golabi-Behmel syndromes

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Mouse mutant embryos overexpre ...... impson-Golabi-Behmel syndromes

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Genes & Development

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Mouse mutant embryos overexpre ...... impson-Golabi-Behmel syndromes

@en

P2093

A Efstratiadis

http://www.w3.org/2001/XMLSchema#string

J Eggenschwiler

http://www.w3.org/2001/XMLSchema#string

P A Leighton

http://www.w3.org/2001/XMLSchema#string

P Fisher

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S M Tilghman

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T Ludwig

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P2860

Parental imprinting of the mouse H19 gene

Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

Embryology of Exomphalos and Allied Malformations

Monoallelic expression of the human H19 gene

Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature

Disruption of imprinting caused by deletion of the H19 gene region in mice

Molecular and cellular aspects of the insulin-like growth factor I receptor

An enhancer deletion affects both H19 and Igf2 expression

An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

Disruption of the Hoxd-13 gene induces localized heterochrony leading to mice with neotenic limbs

P304

3128-3142

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scholarly article

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10.1101/GAD.11.23.3128

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23

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11

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13839720

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9389646

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316748

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