about
Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndromeNKX2-5 regulates the expression of beta-catenin and GATA4 in ventricular myocytesmiR-126 regulates angiogenic signaling and vascular integrityThe functional landscape of mouse gene expressionTbx20 dose-dependently regulates transcription factor networks required for mouse heart and motoneuron developmentCooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heartCardiac T-box factor Tbx20 directly interacts with Nkx2-5, GATA4, and GATA5 in regulation of gene expression in the developing heartTbx5-dependent rheostatic control of cardiac gene expression and morphogenesisTinman/Nkx2-5 acts via miR-1 and upstream of Cdc42 to regulate heart function across speciesTbx5 is essential for forelimb bud initiation following patterning of the limb field in the mouse embryoReptilian heart development and the molecular basis of cardiac chamber evolutionThe homeodomain transcription factor Irx5 establishes the mouse cardiac ventricular repolarization gradientRegulation of retinal interneuron subtype identity by the Iroquois homeobox gene Irx6Baf60c is essential for function of BAF chromatin remodelling complexes in heart developmentLats2/Kpm is required for embryonic development, proliferation control and genomic integrityBaf60c is a nuclear Notch signaling component required for the establishment of left-right asymmetry.Chromatin remodelling complex dosage modulates transcription factor function in heart developmentIroquois homeobox gene 3 establishes fast conduction in the cardiac His-Purkinje network.A Slit/miR-218/Robo regulatory loop is required during heart tube formation in zebrafish.Extensive enteric nervous system abnormalities in mice transgenic for artificial chromosomes containing Parkinson disease-associated alpha-synuclein gene mutations precede central nervous system changes.Serum response factor, an enriched cardiac mesoderm obligatory factor, is a downstream gene target for Tbx genes.TBX5 mutations and congenital heart disease: Holt-Oram syndrome revealed.Tbx5-dependent pathway regulating diastolic function in congenital heart disease.The developmental genetics of congenital heart disease.Atrial natriuretic factor in the developing heart: a signpost for cardiac morphogenesis.Epigenetics and cardiovascular development.Iroquois homeodomain transcription factors in heart development and function.ATP-dependent chromatin remodeling during mammalian development.Mechanical and neuroendocrine regulation of the endocrine heart.Epigenetic repression of cardiac progenitor gene expression by Ezh2 is required for postnatal cardiac homeostasis.Dynamic and coordinated epigenetic regulation of developmental transitions in the cardiac lineage.Shox2 mediates Tbx5 activity by regulating Bmp4 in the pacemaker region of the developing heart.The heart's Da Vinci code: a Renaissance at Keystone.Cardiac-enriched BAF chromatin-remodeling complex subunit Baf60c regulates gene expression programs essential for heart development and function.A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome.Regulation of chamber-specific gene expression in the developing heart by Irx4.Ezh2 regulates anteroposterior axis specification and proximodistal axis elongation in the developing limb.Genome-wide analysis of mouse transcripts using exon microarrays and factor graphs.Chromatin remodeling in heart development.
P50
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P50
description
hulumtues
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onderzoeker
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հետազոտող
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Benoit G. Bruneau
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Benoit G. Bruneau
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Benoit G. Bruneau
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Benoit G. Bruneau
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Benoit G. Bruneau
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type
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Benoit G. Bruneau
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Benoit G. Bruneau
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Benoit G. Bruneau
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Benoit G. Bruneau
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Benoit G. Bruneau
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prefLabel
Benoit G. Bruneau
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Benoit G. Bruneau
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Benoit G. Bruneau
@es
Benoit G. Bruneau
@nl
Benoit G. Bruneau
@sl
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0000 0001 3846 6306
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nb2012009427
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0000-0002-0804-7597
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lccn-nb2012009427