| scholarly article | Q13442814 |
| P2093 | author name string | Jill A Rosenfeld | |
| Valerie K Jordan | |||
| Seema R Lalani | |||
| Daryl A Scott | |||
| P2860 | cites work | Cardiovascular basic helix loop helix factor 1, a novel transcriptional repressor expressed preferentially in the developing and adult cardiovascular system | Q22253240 |
| Tetralogy of fallot and other congenital heart defects in Hey2 mutant mice | Q24310111 | ||
| CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila | Q24315560 | ||
| GATA4 loss-of-function mutations underlie familial tetralogy of fallot | Q24321906 | ||
| Hey basic helix-loop-helix transcription factors are repressors of GATA4 and GATA6 and restrict expression of the GATA target gene ANF in fetal hearts | Q24337426 | ||
| Identification and expression of a novel family of bHLH cDNAs related to Drosophila hairy and enhancer of split | Q28139474 | ||
| Hey genes: a novel subfamily of hairy- and Enhancer of split related genes specifically expressed during mouse embryogenesis | Q28140345 | ||
| Phenotypic variability in Hey2 -/- mice and absence of HEY2 mutations in patients with congenital heart defects or Alagille syndrome | Q28283975 | ||
| Oscillating expression of c-Hey2 in the presomitic mesoderm suggests that the segmentation clock may use combinatorial signaling through multiple interacting bHLH factors | Q28510928 | ||
| HRT1, HRT2, and HRT3: a new subclass of bHLH transcription factors marking specific cardiac, somitic, and pharyngeal arch segments | Q28587806 | ||
| Integrated detection and population-genetic analysis of SNPs and copy number variation | Q29614584 | ||
| High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications. | Q33480832 | ||
| Ventricular septal defect and cardiomyopathy in mice lacking the transcription factor CHF1/Hey2. | Q34415806 | ||
| High resolution discovery and confirmation of copy number variants in 90 Yoruba Nigerians | Q34964608 | ||
| Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions. | Q36403958 | ||
| Population analysis of large copy number variants and hotspots of human genetic disease | Q37156109 | ||
| Hey bHLH transcription factors | Q38253508 | ||
| SgD-CNV, a database for common and rare copy number variants in three Asian populations | Q44620603 | ||
| The basic helix-loop-helix genes Hesr1/Hey1 and Hesr2/Hey2 regulate maintenance of neural precursor cells in the brain | Q44831571 | ||
| Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development | Q48318063 | ||
| A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot. | Q50946634 | ||
| Mouse gridlock | Q58298447 | ||
| Genome-wide oligonucleotide-based array comparative genome hybridization analysis of non-isolated congenital diaphragmatic hernia | Q79518248 | ||
| The spectrum of cardiovascular anomalies in CHF1/Hey2 deficient mice reveals roles in endocardial cushion, myocardial and vascular maturation | Q81387718 | ||
| HEY2 mutations in malformed hearts | Q81576274 | ||
| Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters | Q85028767 | ||
| Investigation of NRXN1 deletions: clinical and molecular characterization | Q86393147 | ||
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 2145-2149 | |
| P577 | publication date | 2015-04-01 | |
| P1433 | published in | American Journal of Medical Genetics | Q4744254 |
| P1476 | title | Duplication of HEY2 in cardiac and neurologic development. | |
| P478 | volume | 167A |
| Q49893514 | Notch signaling regulates Hey2 expression in a spatiotemporal dependent manner during cardiac morphogenesis and trabecular specification. |
| Q47676203 | Perivascular neurotransmitters: Regulation of cerebral blood flow and role in primary headaches. |
| Q90735529 | Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot |
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