A Type 3 Gaucher-Like Disease Due To Saposin C Deficiency in Two Emirati Families Caused by a Novel Splice Site Variant in the PSAP Gene
Mohamed, Feda E., Ali, Amanat, Al-Tenaiji, Amal, Al-Jasmi, Amina, Al-Jasmi, Fatma
Published in Journal of molecular neuroscience (01.06.2022)
Published in Journal of molecular neuroscience (01.06.2022)
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The double whammy of ER-retention and dominant-negative effects in numerous autosomal dominant diseases: significance in disease mechanisms and therapy
Gariballa, Nesrin, Mohamed, Feda, Badawi, Sally, Ali, Bassam R
Published in Journal of biomedical science (27.06.2024)
Published in Journal of biomedical science (27.06.2024)
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The Discovery of Small Allosteric and Active Site Inhibitors of the SARS-CoV-2 Main Protease via Structure-Based Virtual Screening and Biological Evaluation
Mahgoub, Radwa E, Mohamed, Feda E, Alzyoud, Lara, Ali, Bassam R, Ferreira, Juliana, Rabeh, Wael M, AlNeyadi, Shaikha S, Atatreh, Noor, Ghattas, Mohammad A
Published in Molecules (Basel, Switzerland) (01.10.2022)
Published in Molecules (Basel, Switzerland) (01.10.2022)
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Expanding the clinical spectrum of cytosolic phosphoenolpyruvate carboxykinase deficiency: novel PCK1 variants in four Arabian Gulf families
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
Published in Orphanet journal of rare diseases (03.11.2023)
Published in Orphanet journal of rare diseases (03.11.2023)
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Discovery of pyrimidoindol and benzylpyrrolyl inhibitors targeting SARS-CoV-2 main protease (M pro ) through pharmacophore modelling, covalent docking, and biological evaluation
Mahgoub, Radwa E, Mohamed, Feda E, Ali, Bassam R, Ferreira, Juliana, Rabeh, Wael M, Atatreh, Noor, Ghattas, Mohammad A
Published in Journal of molecular graphics & modelling (01.03.2024)
Published in Journal of molecular graphics & modelling (01.03.2024)
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The Discovery of Novel Small Oxindole‐Based Inhibitors Targeting the SARS‐CoV‐2 Main Protease (Mpro)
Alzyoud, Lara, Mahgoub, Radwa E., Mohamed, Feda E., Ali, Bassam R., Ferreira, Juliana, Rabeh, Wael M., Atatreh, Noor, Ghattas, Mohammad A.
Published in Chemistry & biodiversity (01.11.2023)
Published in Chemistry & biodiversity (01.11.2023)
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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 analysis
Mohamed, Feda E, Ghattas, Mohammad A, Almansoori, Taleb M, Tabouni, Mohammed, Baydoun, Ibrahim, Kizhakkedath, Praseetha, John, Anne, Alblooshi, Hiba, Shaukat, Qudsia, Al-Jasmi, Fatma
Published in Frontiers in pediatrics (12.07.2023)
Published in Frontiers in pediatrics (12.07.2023)
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