<p>In the model, the triangle represents the <i>Mef2c-AHF-Cre</i> lineage and the <i>Tbx1</i> expression pattern, before migrating into the heart tube at E9.5. Left panel: <i>Tbx1</i> expression is strongest in the AHF and weakest in the posterior SHF (pSHF) while <i>Wnt/β-catenin</i> expression is opposite. Left panel depicts a possible double negative feedback loop between the two genes in the SHF, required for normal cardiac outflow tract (OFT) formation. Middle panel shows increased differentiation in the AHF when <i>Tbx1</i> is inactivated or <i>β-catenin</i> is constitutively active in the AHF. This results in premature differentiation within this tissue. Right panel depicts the rescue genotype in which both alleles of <i>Tbx1</i> and...
<p>(A) Comparison of global gene expression changes in the micro-dissected AHF of <i>β-catenin GOF</...
<p>(A–D) Immunohistochemistry using an anti-cleaved Caspase 3 antibody showed no obvious difference ...
<p>Phenotypes in embryos in which one <i>β-catenin</i> loss of function allele to either <i>Mef2c-AH...
<div><p>The 22q11.2 deletion syndrome (22q11.2DS; velo-cardio-facial syndrome; DiGeorge syndrome) is...
AbstractTbx1, a T-box transcription factor, and an important gene for velo-cardio-facial syndrome/Di...
Tbx1 is required for the expansion of second heart field (SHF) cardiac progenitors destined to the o...
Tbx1 is required for the expansion of second heart field (SHF) cardiac progenitors destined to the o...
Tbx1 is required for the expansion of second heart field (SHF) cardiac progenitors destined to the o...
<div><p>Mutations of the <em>Wnt5a</em> gene, encoding a ligand of the non-canonical Wnt pathway, an...
Tbx1 is required for the expansion of second heart field (SHF) cardiac progenitors destined to the o...
Mutations of the Wnt5a gene, encoding a ligand of the non-canonical Wnt pathway, and the Ror2 gene, ...
Mutations of the Wnt5a gene, encoding a ligand of the non-canonical Wnt pathway, and the Ror2 gene, ...
Mutations of the Wnt5a gene, encoding a ligand of the non-canonical Wnt pathway, and the Ror2 gene, ...
Mutations of the Wnt5a gene, encoding a ligand of the non-canonical Wnt pathway, and the Ror2 gene, ...
International audienceRATIONALE:Cardiac progenitor cells from the second heart field (SHF) contribut...
<p>(A) Comparison of global gene expression changes in the micro-dissected AHF of <i>β-catenin GOF</...
<p>(A–D) Immunohistochemistry using an anti-cleaved Caspase 3 antibody showed no obvious difference ...
<p>Phenotypes in embryos in which one <i>β-catenin</i> loss of function allele to either <i>Mef2c-AH...
<div><p>The 22q11.2 deletion syndrome (22q11.2DS; velo-cardio-facial syndrome; DiGeorge syndrome) is...
AbstractTbx1, a T-box transcription factor, and an important gene for velo-cardio-facial syndrome/Di...
Tbx1 is required for the expansion of second heart field (SHF) cardiac progenitors destined to the o...
Tbx1 is required for the expansion of second heart field (SHF) cardiac progenitors destined to the o...
Tbx1 is required for the expansion of second heart field (SHF) cardiac progenitors destined to the o...
<div><p>Mutations of the <em>Wnt5a</em> gene, encoding a ligand of the non-canonical Wnt pathway, an...
Tbx1 is required for the expansion of second heart field (SHF) cardiac progenitors destined to the o...
Mutations of the Wnt5a gene, encoding a ligand of the non-canonical Wnt pathway, and the Ror2 gene, ...
Mutations of the Wnt5a gene, encoding a ligand of the non-canonical Wnt pathway, and the Ror2 gene, ...
Mutations of the Wnt5a gene, encoding a ligand of the non-canonical Wnt pathway, and the Ror2 gene, ...
Mutations of the Wnt5a gene, encoding a ligand of the non-canonical Wnt pathway, and the Ror2 gene, ...
International audienceRATIONALE:Cardiac progenitor cells from the second heart field (SHF) contribut...
<p>(A) Comparison of global gene expression changes in the micro-dissected AHF of <i>β-catenin GOF</...
<p>(A–D) Immunohistochemistry using an anti-cleaved Caspase 3 antibody showed no obvious difference ...
<p>Phenotypes in embryos in which one <i>β-catenin</i> loss of function allele to either <i>Mef2c-AH...