Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder.
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Determination of genetic predisposition to patent ductus arteriosus in preterm infantsMyocardin regulates expression of contractile genes in smooth muscle cells and is required for closure of the ductus arteriosus in miceA heart-hand syndrome gene: Tfap2b plays a critical role in the development and remodeling of mouse ductus arteriosus and limb patterningTfAP-2 is required for night sleep in Drosophila.MicroRNAs in the Myocyte Enhancer Factor 2 (MEF2)-regulated Gtl2-Dio3 Noncoding RNA Locus Promote Cardiomyocyte Proliferation by Targeting the Transcriptional Coactivator Cited2.Genetic basis of congenital cardiovascular malformationsPatterns of gene expression in the ductus arteriosus are related to environmental and genetic risk factors for persistent ductus patency.Mutations of TFAP2B in congenital heart disease patients in Mysore, South India.Characterization of transcription factor AP-2 β mutations involved in familial isolated patent ductus arteriosus suggests haploinsufficiency.A Conserved GEF for Rho-Family GTPases Acts in an EGF Signaling Pathway to Promote Sleep-like Quiescence in Caenorhabditis elegans.Sleep-active neuron specification and sleep induction require FLP-11 neuropeptides to systemically induce sleep.Mutations in the Histone Modifier PRDM6 Are Associated with Isolated Nonsyndromic Patent Ductus ArteriosusAnalysis of TFAP2A mutations in Branchio-Oculo-Facial Syndrome indicates functional complexity within the AP-2α DNA-binding domainBicuspid aortic valve: clinical approach and scientific review of a common clinical entity.Conditional deletion of AP-2β in mouse cranial neural crest results in anterior segment dysgenesis and early-onset glaucoma.Frontal nasal prominence expression driven by Tcfap2a relies on a conserved binding site for STAT proteins.Transcription factor pathways and congenital heart disease.TFAP2B mutation and dental anomalies.Patent ductus arteriosus and pulmonary valve stenosis in a patient with 18p deletion syndrome.Gene expression profiling of human primary astrocytes exposed to manganese chloride indicates selective effects on several functions of the cells.Familial nonsyndromic patent ductus arteriosus caused by mutations in TFAP2B.Sleep-Active Neurons: Conserved Motors of Sleep.The Changing Landscape in the Genetic Etiology of Human Tooth Agenesis.Single nucleotide polymorphisms inAGTR1,TFAP2B, andTRAF1are not associated with the incidence of patent ductus arteriosus in Japanese preterm infants
P2860
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P2860
Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder.
description
2005 nî lūn-bûn
@nan
2005 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Syndromic patent ductus arteri ...... on of a linked sleep disorder.
@ast
Syndromic patent ductus arteri ...... on of a linked sleep disorder.
@en
type
label
Syndromic patent ductus arteri ...... on of a linked sleep disorder.
@ast
Syndromic patent ductus arteri ...... on of a linked sleep disorder.
@en
prefLabel
Syndromic patent ductus arteri ...... on of a linked sleep disorder.
@ast
Syndromic patent ductus arteri ...... on of a linked sleep disorder.
@en
P2093
P2860
P356
P1476
Syndromic patent ductus arteri ...... on of a linked sleep disorder.
@en
P2093
Anita Farhi
Barbara Pober
Carol Nelson-Williams
Carole A Warnes
Jayaram Radhakrishnan
Khary S Carew
Matthew W State
Richard P Lifton
Ronald W Day
P2860
P304
P356
10.1073/PNAS.0409852102
P407
P577
2005-01-31T00:00:00Z