Characterization of ACE2 naturally occurring missense variants: impact on subcellular localization and trafficking

por Badawi, Sally, Mohamed, Feda E., Alkhofash, Nesreen R., John, Anne, Ali, Amanat, Ali, Bassam R.
Publicado 2022

Novel compound heterozygous variants (c.971delA/c.542C > T) in SLC1A4 causes spastic tetraplegia, thin corpus callosum, and progressive microcephaly: a case report and mutational a...

por Mohamed, Feda E., Ghattas, Mohammad A., Almansoori, Taleb M., Tabouni, Mohammed, Baydoun, Ibrahim, Kizhakkedath, Praseetha, John, Anne, Alblooshi, Hiba, Shaukat, Qudsia, Al-Jasmi, Fatma
Publicado 2023

The Discovery of Small Allosteric and Active Site Inhibitors of the SARS-CoV-2 Main Protease via Structure-Based Virtual Screening and Biological Evaluation

por Mahgoub, Radwa E., Mohamed, Feda E., Alzyoud, Lara, Ali, Bassam R., Ferreira, Juliana, Rabeh, Wael M., AlNeyadi, Shaikha S., Atatreh, Noor, Ghattas, Mohammad A.
Publicado 2022

Expanding the clinical spectrum of cytosolic phosphoenolpyruvate carboxykinase deficiency: novel PCK1 variants in four Arabian Gulf families

por Al Busaidi, Marwa, Mohamed, Feda E., Al-Ajmi, Eiman, Al Hashmi, Nadia, Al-Thihli, Khalid, Al Futaisi, Amna, Al Mamari, Watfa, Al-Murshedi, Fathiya, Al-Jasmi, Fatma
Publicado 2023