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Cell Reports|December 15, 2021
The onset of circulation triggers a metabolic switch required for endothelial to hematopoietic transitionEmanuele Azzoni, Vincent Frontera, Giorgio Anselmi, et al.Nature Communications|June 9, 2021
Maternal iron deficiency perturbs embryonic cardiovascular development in miceJacinta I Kalisch-Smith, Nikita Ved, Dorota Szumska, et al.Human Molecular Genetics|December 10, 2019
Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variantsGavin Chapman, Julie L M Moreau, Eddie I P, et al.Human Molecular Genetics|December 4, 2020
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and miceElla M M A Martin, Annabelle Enriquez, Duncan B Sparrow, et al.The New England Journal of Medicine|August 10, 2017
NAD Deficiency, Congenital Malformations, and Niacin SupplementationHongjun Shi, Annabelle Enriquez, Melissa Rapadas, et al.Pageof 5