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               <mods:identifier type="citation">J Cardiovasc Dev Dis. 2024 Jul 15;11(7):223.</mods:identifier>
               <mods:identifier type="journal">Journal of Cardiovascular Development and Disease</mods:identifier>
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               <mods:abstract>Genome-wide association studies and experimental mouse models implicate the  and  genes in congenital heart disease (CHD). Their close physical proximity and conserved synteny suggest that these two genes might be involved in analogous cardiac developmental processes. Heterozygous  loss-of-function mutations alone or humanized  mutations in a NOTCH1-sensitized genetic background cause bicuspid aortic valve (BAV) and a membranous ventricular septal defect (VSD), consistent with MIB1 and NOTCH1 functioning in the same pathway. To determine if MIB1-NOTCH and GATA6 interact in valvular and septal development, we generated compound heterozygote mice carrying different Mib1  ( and ) or  () mutations with the  heterozygous null mutation. Combining  or  with  does not affect  single mutant phenotypes. In contrast, combining  with  decreases the incidence of BAV and VSD by 50%, suggesting a suppressive effect of  on . Transcriptomic and functional analyses revealed that while the EMT pathway term is depleted in the  mutant, introducing the  variant robustly enriches this term, consistent with the  phenotypic suppression of . Interestingly, combined  and  insufficiency led to a nearly fully penetrant VSD but did not affect the BAV phenotype, underscoring the complex functional relationship between MIB1, NOTCH, and GATA6 in valvular and septal development.</mods:abstract>
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                  <mods:topic>BAV</mods:topic>
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                  <mods:title>Intricate MIB1-NOTCH-GATA6 Interactions in Cardiac Valvular and Septal Development.</mods:title>
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