Common variation in ISL1 confers genetic susceptibility for human congenital heart disease.

por Kristen N Stevens, Hakon Hakonarson, Cecilia E Kim, Pieter A Doevendans, Bobby P C Koeleman, Seema Mital, Jennifer Raue, Joseph T Glessner, John G Coles, Victor Moreno, Anne Granger, Stephen B Gruber, Peter J Gruber
Publicado 2010

Amnion signals are essential for mesoderm formation in primates

por Ran Yang, Alexander Goedel, Yu Kang, Chenyang Si, Chu Chu, Yi Zheng, Zhenzhen Chen, Peter J. Gruber, Yao Xiao, Chikai Zhou, Nevin Witman, Elif Eroglu, Chuen-Yan Leung, Yongchang Chen, Jianping Fu, Weizhi Ji, Fredrik Lanner, Yuyu Niu, Kenneth R. Chien
Publicado 2021

Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

por Cristina E. Trevino, Aaron M. Holleman, Holly Corbitt, Cheryl L. Maslen, Tracie C. Rosser, David J. Cutler, H. Richard Johnston, Benjamin L. Rambo-Martin, Jai Oberoi, Kenneth J. Dooley, George T. Capone, Roger H. Reeves, Heather J. Cordell, Bernard D. Keavney, A. J. Agopian, Elizabeth Goldmuntz, Peter J. Gruber, James E. O’Brien, Douglas C. Bittel, Lalita Wadhwa, Clifford L. Cua, Ivan P. Moskowitz, Jennifer G. Mulle, Michael P. Epstein, Stephanie L. Sherman, Michael E. Zwick
Publicado 2021