Variable predicted pathogenic mechanisms for novel MECP2 variants in RTT patients

por Sharaf-Eldin, Wessam E., Issa, Mahmoud Y., Zaki, Maha S., Kilany, Ayman, Fayez, Alaaeldin G.
Publicado 2022

A Novel Loss-of-Sclerostin Function Mutation in a First Egyptian Family with Sclerosteosis

por Fayez, Alaaeldin, Aglan, Mona, Esmaiel, Nora, El Zanaty, Taher, Abdel Kader, Mohamed, El Ruby, Mona
Publicado 2015

Independent of DAZL-T54A variant and AZF microdeletion in a sample of Egyptian patients with idiopathic non-obstructed azoospermia

por Shafae, Mohammed M El, Sabry, Jehan H, Behiry, Eman G, Sabry, Hanan H, Salim, Mona A, Fayez, Alaaeldin G
Publicado 2018

miR-454-3p and miR-194-5p targeting cardiac sarcolemma ion exchange transcripts are potential noninvasive diagnostic biomarkers for childhood dilated cardiomyopathy in Egyptian pat...

por Fayez, Alaaeldin G., Esmaiel, Nora N., Salem, Sohair M., Ashaat, Engy A., El-Saiedi, Sonia A., El Ruby, Mona O.
Publicado 2022

New drug-like small molecule antagonizes phosphatidylinositol (3,4,5)-trisphosphate (PIP3) in patients with conotruncal heart defects

por Fayez, Alaaeldin G., Esmaiel, Nora N., Ashaat, Engy A., Refeat, Miral M., Lotfy, Randa S., Raouf, Haiam Abdel, El Ruby, Mona O.
Publicado 2023

Dynamic disequilibrium-based pathogenicity model in mutated pyrin’s B30.2 domain—Casp1/p20 complex

por Fayez, Alaaeldin G., Eldeen, Ghada Nour, Zarouk, Waheba A., Hamed, Khaled, Ramadan, Abeer, Foda, Bardees M., Kobesiy, Maha M., Zekrie, Mai E., Lotfy, Randa S., Sokkar, Mona F., El-Bassyouni, Hala T.
Publicado 2022

DALIA- a comprehensive resource of Disease Alleles in Arab population

por Vatsyayan, Aastha, Sharma, Parul, Gupta, Shrey, Sandhu, Sumiti, Venu, Seetha Lakshmi, Sharma, Vandana, Badaoui, Bouabid, Azedine, Kaidi, Youssef, Serti, Rajab, Anna, Fayez, Alaaeldin, Madinur, Seema, Ranawat, Anop, Pandhare, Kavita, Ramachandran, Srinivasan, Sivasubbu, Sridhar, Scaria, Vinod
Publicado 2021