Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD).
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Human SP-A1 (SFTPA1) variant-specific 3' UTRs and poly(A) tail differentially affect the in vitro translation of a reporter geneChromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic herniaEffect of Structural Changes in Proteins Derived from GATA4 Nonsynonymous Single Nucleotide Polymorphisms in Congenital Heart Disease.POEM, A 3-dimensional exon taxonomy and patterns in untranslated exons.Role of 5'- and 3'-untranslated regions of mRNAs in human diseases.Wnt signaling pathway pharmacogenetics in non-small cell lung cancerIdentification of functional mutations in GATA4 in patients with congenital heart diseaseA GATA4-regulated tumor suppressor network represses formation of malignant human astrocytomas.c.620C>T mutation in GATA4 is associated with congenital heart disease in South India.GATA4 expression is primarily regulated via a miR-26b-dependent post-transcriptional mechanism during cardiac hypertrophyDifferences in Copy Number Variation between Discordant Monozygotic Twins as a Model for Exploring Chromosomal Mosaicism in Congenital Heart Defects.A Rapid, High-Quality, Cost-Effective, Comprehensive and Expandable Targeted Next-Generation Sequencing Assay for Inherited Heart Diseases.Identification of MEF2B and TRHDE Gene Polymorphisms Related to Growth Traits in a New Ujumqin Sheep Population.Single nucleotide polymorphism of NKX2-5 gene with sporadic congenital heart disease in Chinese Bai population.Mutational screening of affected cardiac tissues and peripheral blood cells identified novel somatic mutations in GATA4 in patients with ventricular septal defectA gain-of-function ACTC1 3'UTR mutation that introduces a miR-139-5p target site may be associated with a dominant familial atrial septal defect.Investigation of somatic NKX2-5 mutations in congenital heart diseaseA study of the role of GATA4 polymorphism in cardiovascular metabolic disorders.The oligodeoxynucleotide probes for the site-specific modification of RNA.Transcription factor pathways and congenital heart disease.Impaired pre-mRNA processing and altered architecture of 3' untranslated regions contribute to the development of human disorders.Congenital heart diseases and their association with the variant distribution features on susceptibility genes.Congenital heart disease: the crossroads of genetics, epigenetics and environment.Associations of GATA4 genetic mutations with the risk of congenital heart disease: A meta-analysis.Muscle connective tissue controls development of the diaphragm and is a source of congenital diaphragmatic hernias.Functional characterization of CDK5 and CDK5R1 mutations identified in patients with non-syndromic intellectual disability.Expression and functional analysis of NUCLEAR FACTOR-Y, subunit B genes in barley.GATA4 is a regulator of astrocyte cell proliferation and apoptosis in the human and murine central nervous system.Analysis of the microRNA signature in left atrium from patients with valvular heart disease reveals their implications in atrial fibrillation.Investigating ANKH and ENPP1 in Slovakian families with chondrocalcinosis
P2860
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P2860
Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD).
description
2007 nî lūn-bûn
@nan
2007 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Mutations in the 3'-untranslat ...... ongenital heart disease (CHD).
@ast
Mutations in the 3'-untranslat ...... ongenital heart disease (CHD).
@en
Mutations in the 3'-untranslat ...... s for congenital heart disease
@nl
type
label
Mutations in the 3'-untranslat ...... ongenital heart disease (CHD).
@ast
Mutations in the 3'-untranslat ...... ongenital heart disease (CHD).
@en
Mutations in the 3'-untranslat ...... s for congenital heart disease
@nl
prefLabel
Mutations in the 3'-untranslat ...... ongenital heart disease (CHD).
@ast
Mutations in the 3'-untranslat ...... ongenital heart disease (CHD).
@en
Mutations in the 3'-untranslat ...... s for congenital heart disease
@nl
P2093
P2860
P356
P1433
P1476
Mutations in the 3'-untranslat ...... ongenital heart disease (CHD).
@en
P2093
Juergen Borlak
Si-Hyen Cho
Stella Marie Reamon-Buettner
P2860
P2888
P356
10.1186/1471-2350-8-38
P577
2007-06-25T00:00:00Z
P5875
P6179
1033231091