Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency. - Wikidata - wikimedia - TriplyDB

Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency.

Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency.

http://www.wikidata.org/entity/Q36802947

about

Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome The cardiac transcription network modulated by Gata4, Mef2a, Nkx2.5, Srf, histone modifications, and microRNAs A novel role for transcription factor Lmo4 in thymus development through genetic interaction with Cited2 Maternal high-fat diet interacts with embryonic Cited2 genotype to reduce Pitx2c expression and enhance penetrance of left-right patterning defects.TCreERT2, a transgenic mouse line for temporal control of Cre-mediated recombination in lineages emerging from the primitive streak or tail bud.Mice carrying a hypomorphic Evi1 allele are embryonic viable but exhibit severe congenital heart defects Acute loss of Cited2 impairs Nanog expression and decreases self-renewal of mouse embryonic stem cells Cited2 gene controls pluripotency and cardiomyocyte differentiation of murine embryonic stem cells through Oct4 gene High-throughput analysis of mouse embryos by magnetic resonance imaging A cell-autonomous role of Cited2 in controlling myocardial and coronary vascular development.CITED2 Cooperates with ISL1 and Promotes Cardiac Differentiation of Mouse Embryonic Stem Cells.CITED2 mutation and methylation in children with congenital heart disease Mechanism responsible for D-transposition of the great arteries: Is this part of the spectrum of right isomerism?Cited2 is an essential regulator of adult hematopoietic stem cells Left Right Patterning, Evolution and Cardiac Development.

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P2860

Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency.

http://www.wikidata.org/entity/Q36802947

description

2008 nî lūn-bûn

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2008年の論文

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2008年論文

@yue

2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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2008年论文

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2008年论文

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name

Epiblastic Cited2 deficiency r ...... hanism for haploinsufficiency.

@ast

Epiblastic Cited2 deficiency r ...... hanism for haploinsufficiency.

@en

type

label

Epiblastic Cited2 deficiency r ...... hanism for haploinsufficiency.

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Epiblastic Cited2 deficiency r ...... hanism for haploinsufficiency.

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prefLabel

Epiblastic Cited2 deficiency r ...... hanism for haploinsufficiency.

@ast

Epiblastic Cited2 deficiency r ...... hanism for haploinsufficiency.

@en

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P1433

Cardiovascular Research

P1476

Epiblastic Cited2 deficiency r ...... hanism for haploinsufficiency.

@en

P2093

Angela Franklyn

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

Carol Broadbent

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Cassandra R Farthing

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

Jürgen E Schneider

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

Mark Lewandoski

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

Yumiko Saga

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

P2860

Functional role of p35srj, a novel p300/CBP binding protein, during transactivation by HIF-1

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects

Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator

Physical and functional interactions among AP-2 transcription factors, p300/CREB-binding protein, and CITED2

Identification and functional analysis of CITED2 mutations in patients with congenital heart defects

Identification of the CREB-binding protein/p300-interacting protein CITED2 as a peroxisome proliferator-activated receptor alpha coregulator

X-linked situs abnormalities result from mutations in ZIC3

Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects.

Identification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging technique

P304

448-457

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scholarly article

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10.1093/CVR/CVN101

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3

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P478

79

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P50

Simon T. MacDonald

Simon D Bamforth

Shoumo Bhattacharya

Chiann-Mun Chen

P577

2008-04-25T00:00:00Z

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P5875

5411392

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18440989

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P921

haploinsufficiency

P932

2492730

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