GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling
about
Of mice and men: molecular genetics of congenital heart diseaseThe neural crest in cardiac congenital anomaliesThe emerging role of GATA transcription factors in development and diseaseBrg1 governs distinct pathways to direct multiple aspects of mammalian neural crest cell developmentEfficient Software for Multi-marker, Region-Based Analysis of GWAS Data.The High Mobility Group A1 (HMGA1) Transcriptome in Cancer and Development.GATA6 haploinsufficiency causes pancreatic agenesis in humans.A novel mutation in GATA6 causes pancreatic agenesisNovel and functional DNA sequence variants within the GATA6 gene promoter in ventricular septal defects.Identification of GATA6 sequence variants in patients with congenital heart defects.Genome-wide expression analysis in fibroblast cell lines from probands with Pallister Killian syndromeRare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathwaysSOX4 transcriptionally regulates multiple SEMA3/plexin family members and promotes tumor growth in pancreatic cancerMFAP5 loss-of-function mutations underscore the involvement of matrix alteration in the pathogenesis of familial thoracic aortic aneurysms and dissectionsSema3C promotes the survival and tumorigenicity of glioma stem cells through Rac1 activation.Loss of Gata5 in mice leads to bicuspid aortic valve.The Unc-5 Receptor Is Directly Regulated by Tinman in the Developing Drosophila Dorsal Vessel.Exome analysis of a family with pleiotropic congenital heart disease.Neuropilin-2/Semaphorin-3F-mediated repulsion promotes inner hair cell innervation by spiral ganglion neurons.New Genetic Insights into Congenital Heart Disease.Partitioning the heart: mechanisms of cardiac septation and valve developmentHuman gene copy number spectra analysis in congenital heart malformationsNovel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of fallotImpact of Mendelian inheritance in cardiovascular disease.GATA5 loss-of-function mutations underlie tetralogy of fallot.GATA6 mutations cause a broad phenotypic spectrum of diabetes from pancreatic agenesis to adult-onset diabetes without exocrine insufficiencyRac1 Signaling Is Required for Anterior Second Heart Field Cellular Organization and Cardiac Outflow Tract Development.iPSC-derived cardiomyocytes reveal abnormal TGF-β signalling in left ventricular non-compaction cardiomyopathy.Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation.Tbx1, subpulmonary myocardium and conotruncal congenital heart defects.Transcription factor pathways and congenital heart disease.Plexin structures are coming: opportunities for multilevel investigations of semaphorin guidance receptors, their cell signaling mechanisms, and functions.Family-based studies to identify genetic variants that cause congenital heart defects.Cardiac outflow tract anomalies.Morphogenesis and molecular considerations on congenital cardiac septal defects.Congenital diseases and semaphorin signaling: overview to date of the evidence linking them.Pallister-Killian syndrome.GATA-dependent transcriptional and epigenetic control of cardiac lineage specification and differentiation.Unique functions of Gata4 in mouse liver induction and heart developmentTrans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
P2860
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P2860
GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling
description
2009 nî lūn-bûn
@nan
2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
GATA6 mutations cause human ca ...... ng semaphorin-plexin signaling
@ast
GATA6 mutations cause human ca ...... ng semaphorin-plexin signaling
@en
GATA6 mutations cause human ca ...... ng semaphorin-plexin signaling
@en-gb
GATA6 mutations cause human ca ...... ng semaphorin-plexin signaling
@nl
type
label
GATA6 mutations cause human ca ...... ng semaphorin-plexin signaling
@ast
GATA6 mutations cause human ca ...... ng semaphorin-plexin signaling
@en
GATA6 mutations cause human ca ...... ng semaphorin-plexin signaling
@en-gb
GATA6 mutations cause human ca ...... ng semaphorin-plexin signaling
@nl
prefLabel
GATA6 mutations cause human ca ...... ng semaphorin-plexin signaling
@ast
GATA6 mutations cause human ca ...... ng semaphorin-plexin signaling
@en
GATA6 mutations cause human ca ...... ng semaphorin-plexin signaling
@en-gb
GATA6 mutations cause human ca ...... ng semaphorin-plexin signaling
@nl
P2093
P2860
P921
P356
P1476
GATA6 mutations cause human ca ...... ng semaphorin-plexin signaling
@en
P2093
Eiji Yamamura
Hiroyuki Yamagishi
Kazuki Kodo
Kunitaka Joo
Michiko Furutani
Rumiko Matsuoka
Shoichi Arai
Takao Takahashi
Tsutomu Nishizawa
P2860
P304
P356
10.1073/PNAS.0904744106
P407
P577
2009-08-18T00:00:00Z