Mechanisms of T-box gene function in the developing heart. - Test2 - elhamkhani - TriplyDB

Mechanisms of T-box gene function in the developing heart.

Mechanisms of T-box gene function in the developing heart.

http://www.wikidata.org/entity/Q37865969

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Of mice and men: molecular genetics of congenital heart disease The T-box gene family: emerging roles in development, stem cells and cancer The cardiac-restricted protein ADP-ribosylhydrolase-like 1 is essential for heart chamber outgrowth and acts on muscle actin filament assembly Evolution and development of ventricular septation in the amniote heart Functional cardiomyocytes derived from Isl1 cardiac progenitors via Bmp4 stimulation Histone deacetylase 3 modulates Tbx5 activity to regulate early cardiogenesis Lack of genetic interaction between Tbx20 and Tbx3 in early mouse heart development Mitochondrial DNA Hypomethylation Is a Biomarker Associated with Induced Senescence in Human Fetal Heart Mesenchymal Stem Cells.TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus Novel TBX1 loss-of-function mutation causes isolated conotruncal heart defects in Chinese patients without 22q11.2 deletion.Disruption of myocardial Gata4 and Tbx5 results in defects in cardiomyocyte proliferation and atrioventricular septation.Heart fields and cardiac morphogenesis Human breast progenitor cell numbers are regulated by WNT and TBX3.Using potential master regulator sites and paralogous expansion to construct tissue-specific transcriptional networks.Bone Metastasis of Prostate Cancer Can Be Therapeutically Targeted at the TBX2-WNT Signaling Axis.DiGeorge syndrome gene tbx1 functions through wnt11r to regulate heart looping and differentiation The orthologous Tbx transcription factors Omb and TBX2 induce epithelial cell migration and extrusion in vivo without involvement of matrix metalloproteinases Gene expression changes controlling distinct adaptations in the heart and skeletal muscle of a hibernating mammal The inferred cardiogenic gene regulatory network in the mammalian heart.Directed differentiation of patient-specific induced pluripotent stem cells identifies the transcriptional repression and epigenetic modification of NKX2-5, HAND1, and NOTCH1 in hypoplastic left heart syndrome.Tbx20 transcription factor is a downstream mediator for bone morphogenetic protein-10 in regulating cardiac ventricular wall development and function Association between NKX2-5 rs29784 and infantile hypertrophic pyloric stenosis in Chinese Han population.Regulation of skin aging and heart development by TAp63.The drosophila T-box transcription factor midline functions within Insulin/Akt and c-Jun-N terminal kinase stress-reactive signaling pathways to regulate interommatial bristle formation and cell survival.The ulnar-mammary syndrome gene, Tbx3, is a direct target of the retinoic acid signaling pathway, which regulates its expression during mouse limb development Lack of Genetic Interaction between Tbx18 and Tbx2/Tbx20 in Mouse Epicardial Development.Common Variants in the TBX5 Gene Associated with Atrial Fibrillation in a Chinese Han Population.How insights from cardiovascular developmental biology have impacted the care of infants and children with congenital heart disease.Partitioning the heart: mechanisms of cardiac septation and valve development Epigenetic regulation of cardiac development and function by polycomb group and trithorax group proteins Prevalence and Spectrum of TBX5 Mutation in Patients with Lone Atrial Fibrillation.Overexpression of Tbx20 in Adult Cardiomyocytes Promotes Proliferation and Improves Cardiac Function After Myocardial Infarction.Mild decrease in TBX20 promoter activity is a potentially protective factor against congenital heart defects in the Han Chinese population.Early de novo DNA methylation and prolonged demethylation in the muscle lineage.Hypoxia induced the differentiation of Tbx18-positive epicardial cells to CoSMCs Tbx20 acts upstream of Wnt signaling to regulate endocardial cushion formation and valve remodeling during mouse cardiogenesis.T-box family of transcription factor-TBX5, insights in development and disease.Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation.Transcription factor pathways and congenital heart disease.Epicardial progenitor cells in cardiac development and regeneration.

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Mechanisms of T-box gene function in the developing heart.

http://www.wikidata.org/entity/Q37865969

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 14 April 2011

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Mechanisms of T-box gene function in the developing heart.

@en

Mechanisms of T-box gene function in the developing heart.

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type

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Mechanisms of T-box gene function in the developing heart.

@en

Mechanisms of T-box gene function in the developing heart.

@nl

prefLabel

Mechanisms of T-box gene function in the developing heart.

@en

Mechanisms of T-box gene function in the developing heart.

@nl

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Cardiovascular Research

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Mechanisms of T-box gene function in the developing heart.

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Andreas Kispert

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Carsten Rudat

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Franziska Greulich

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P2860

Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation

Hesr1 and Hesr2 regulate atrioventricular boundary formation in the developing heart through the repression of Tbx2

TBX5 nuclear localization is mediated by dual cooperative intramolecular signals

A WW domain protein TAZ is a critical coactivator for TBX5, a transcription factor implicated in Holt-Oram syndrome

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

Characterization of TBX20 in human hearts and its regulation by TFAP2

Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome

T-box transcription factor TBX20 mutations in Chinese patients with congenital heart disease

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scholarly article

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10.1093/CVR/CVR112

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2

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91

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2011-04-14T00:00:00Z

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21498422

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