A Rare Case of the Digenic Inheritance of Long QT Syndrome Type 2 and Type 6

por Heida, Annejet, van der Does, Lisette J. M. E., Ragab, Ahmed A. Y., de Groot, Natasja M. S.
Publicado 2019

The Genetic Puzzle of Familial Atrial Fibrillation

por Ragab, Ahmed A. Y., Sitorus, Gustaf D. S., Brundel, Bianca B. J. J. M., de Groot, Natasja M. S.
Publicado 2020

MD-2 is required for disulfide HMGB1–dependent TLR4 signaling

por Yang, Huan, Wang, Haichao, Ju, Zhongliang, Ragab, Ahmed A., Lundbäck, Peter, Long, Wei, Valdes-Ferrer, Sergio I., He, Mingzhu, Pribis, John P., Li, Jianhua, Lu, Ben, Gero, Domokos, Szabo, Csaba, Antoine, Daniel J., Harris, Helena E., Golenbock, Doug T., Meng, Jianmin, Roth, Jesse, Chavan, Sangeeta S., Andersson, Ulf, Billiar, Timothy R., Tracey, Kevin J., Al-Abed, Yousef
Publicado 2015