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Genetics|April 1, 2016
Penetrance of Congenital Heart Disease in a Mouse Model of Down Syndrome Depends on a Trisomic Potentiator of a Disomic ModifierHuiqing Li, Sarah Edie, Donna Klinedinst, et al.
Journal of Biomaterials Applications|May 19, 2011
Structural and cellular characterization of electrospun recombinant human tropoelastin biomaterialsKathryn A McKenna, Kenton W Gregory, Rebecca C Sarao, et al.
AIMS Genetics|October 21, 2014
Allelic Interaction between CRELD1 and VEGFA in the Pathogenesis of Cardiac Atrioventricular Septal DefectsJennifer K Redig, Gameil T Fouad, Darcie Babcock, et al.
Plos Genetics|October 4, 2018
TIMP3 and TIMP1 are risk genes for bicuspid aortic valve and aortopathy in Turner syndromeHolly Corbitt, Shaine A Morris, Claus H Gravholt, et al.
American Journal of Human Genetics|March 13, 2003
Missense mutations in CRELD1 are associated with cardiac atrioventricular septal defectsSusan W Robinson, Cynthia D Morris, Elizabeth Goldmuntz, et al.
Acta Biomaterialia|August 18, 2011
Mechanical property characterization of electrospun recombinant human tropoelastin for vascular graft biomaterialsKathryn A McKenna, Monica T Hinds, Rebecca C Sarao, et al.
Circulation. Cardiovascular Genetics|April 24, 2012
Genetic modifiers predisposing to congenital heart disease in the sensitized Down syndrome populationHuiqing Li, Sheila Cherry, Donna Klinedinst, et al.
Gene|July 26, 2002
Identification, genomic organization and mRNA expression of CRELD1, the founding member of a unique family of matricellular proteinsPaul A Rupp, Gameil T Fouad, Carley A Egelston, et al.
Human Molecular Genetics|June 25, 2016
Cilia gene mutations cause atrioventricular septal defects by multiple mechanismsOzanna Burnicka-Turek, Jeffrey D Steimle, Wenhui Huang, et al.
American Journal of Human Genetics|October 9, 2012
An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defectsChristine Ackerman, Adam E Locke, Eleanor Feingold, et al.
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