Tetralogy of Fallot and Other Congenital Heart Defects in Hey2 Mutant Mice

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Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

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Mutations in the human Jagged1 gene are responsible for Alagille syndrome

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Gridlock signalling pathway fashions the first embryonic artery

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A mouse model of Alagille syndrome:Notch2as a genetic modifier ofJag1haploinsufficiency

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gridlock , an HLH Gene Required for Assembly of the Aorta in Zebrafish

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HLH proteins, fly neurogenesis, and vertebrate myogenesis

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Vertebrate hairy and Enhancer of split related proteins: transcriptional repressors regulating cellular differentiation and embryonic patterning

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gridlock, a localized heritable vascular patterning defect in the zebrafish

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Familial Tetralogy of Fallot caused by mutation in the jagged1 gene

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Congenital Heart Disease: Incidence and Inheritance

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HRT1, HRT2, and HRT3: A New Subclass of bHLH Transcription Factors Marking Specific Cardiac, Somitic, and Pharyngeal Arch Segments

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Hey genes: a novel subfamily of hairy - and Enhancer of split related genes specifically expressed during mouse embryogenesis

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Comparative Analysis of the Human and Mouse Hey1 Promoter: Hey Genes Are New Notch Target Genes

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Members of the HRT family of basic helix–loop–helix proteins act as transcriptional repressors downstream of Notch signaling

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HERP, a Novel Heterodimer Partner of HES/E(spl) in Notch Signaling

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HERP, a New Primary Target of Notch Regulated by Ligand Binding

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Epidemiology of cardiovascular malformations: Prevalence and risk factors

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Oscillating Expression of c-Hey2 in the Presomitic Mesoderm Suggests That the Segmentation Clock May Use Combinatorial Signaling through Multiple Interacting bHLH Factors

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Jagged1 mutations in patients ascertained with isolated congenital heart defects

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Cardiovascular Basic Helix Loop Helix Factor 1, a Novel Transcriptional Repressor Expressed Preferentially in the Developing and Adult Cardiovascular System

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The Basic Helix-Loop-Helix Transcription Factor HESR1 Regulates Endothelial Cell Tube Formation

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Identification and Expression of a Novel Family of bHLH cDNAs Related to Drosophila Hairy and Enhancer of Split

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Outcome of congenital heart defects - a population-based study

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HERP1 Is a Cell Type-specific Primary Target of Notch

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Genetic basis of syndromes associated with congenital heart disease

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