Data insights from a Moroccan phytochemical database (MPDB) derived from aromatic & medicinal plants by Lamiae, Elkhattabi, Salwa, Zouhdi, Fairouz, Mousstead, Mohtadi, Karima, Fougrach, Hassan, Badri, Wadi, Taki, Hassan, Kettani, Anass, Talbi, Mohammed, Saile, Rachid

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Computational Analysis of nsSNPs of ADA Gene in Severe Combined Immunodeficiency Using Molecular Modeling and Dynamics Simulation by Barakat, Abdelhamid, Abdelghaffar, Houria, Amalou, Ghita, Zouhair, Elkarhat, Elkhattabi, Lamiae, Mehdi Krami, AL, Essadssi, Soukaina, Rouba, Hassan

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In Silico Analysis of Coding/Noncoding SNPs of Human RETN Gene and Characterization of Their Impact on Resistin Stability and Structure by Barakat, Abdelhamid, Rouba, Hassan, Zouhair, Elkarhat, Bouafi, Hind, Amghar, Soumaya, Charoute, Hicham, Morjane, Imane, Elkhattabi, Lamiae, Saile, Rachid

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Association of c.56C > G (rs3135506) Apolipoprotein A5 Gene Polymorphism with Coronary Artery Disease in Moroccan Subjects: A Case-Control Study and an Updated Meta-Analysis by Barakat, Abdelhamid, Saile, Rachid, Benrahma, Houda, Elkhattabi, Lamiae, Ouatou, Sanaa, Charoute, Hicham, Morjane, Imane, Rouba, Hassan

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Potential inhibitors of SARS-cov-2 RNA dependent RNA polymerase protein: molecular docking, molecular dynamics simulations and MM-PBSA analyses by Elkarhat, Zouhair, Charoute, Hicham, Elkhattabi, Lamiae, Barakat, Abdelhamid, Rouba, Hassan

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Structure-based virtual screening to identify hypocholesterolemic phytochemicals as potent inhibitors of squalene synthase a potential target for hypercholesterolemia by Zouhdi, Salwa, Elkhattabi, Lamiae, Moussetad, Fairouz, El Khalfi, Bouchra, Soukri, Abdelaziz, Kettani, Anass, Saile, Rachid

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Omenn syndrome caused by a novel homozygous mutation in recombination activating gene 1 by Benhsaien, Ibtihal, Essadssi, Soukaina, Elkhattabi, Lamiae, Bakhchane, Amina, Abdelghaffar, Houria, Bousfiha, Ahmed Aziz, Badou, Abdallah, Barakat, Abdelhamid

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Computational screening of potential drugs against COVID-19 disease: the Neuropilin-1 receptor as molecular target by Charoute, Hicham, Elkarhat, Zouhair, Elkhattabi, Lamiae, El Fahime, Elmostafa, Oukkache, Naoual, Rouba, Hassan, Barakat, Abdelhamid

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Molecular docking analysis of PPARγ with phytochemicals from Moroccan medicinal plants by Elkhattabi, Lamiae, Zouhdi, Salwa, Moussetad, Fairouz, Kettani, Anass, Barakat, Abdelhamid, Saile, Rachid

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Chromosomal Abnormalities in Patients with Intellectual Disability: A 21-Year Retrospective Study by Belkady, Boutaina, Elkhattabi, Lamiae, Elkarhat, Zouhair, Zarouf, Latifa, Razoki, Lunda, Aboulfaraj, Jamila, Nassereddine, Sanaa, Cadi, Rachida, Rouba, Hassan, Barakat, Abdelhamid

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Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family by Elrharchi, Soukaina, Riahi, Zied, Salime, Sara, Charoute, Hicham, Elkhattabi, Lamiae, Boulouiz, Redouane, Kabine, Mostafa, Bonnet, Crystel, Petit, Christine, Barakat, Abdelhamid

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A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family by Salime, Sara, Riahi, Zied, Elrharchi, Soukaina, Elkhattabi, Lamiae, Charoute, Hicham, Nahili, Halima, Rouba, Hassan, Kabine, Mostafa, Bonnet, Crystel, Petit, Christine, Barakat, Abdelhamid

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Association of c.56C G by Elkhattabi, Lamiae, Charoute, Hicham, Ouatou, Sanaa, Benrahma, Houda, Saile, Rachid, Barakat, Abdelhamid, Morjane, Imane, Rouba, Hassan

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Insights from the SNP analysis of TYMP gene linking MNGIE by Sifeddine, Najat, Elkhattabi, Lamiae, Ait El Cadi, Chaimaa, Krami, Al Mehdi, Mounaji, Khadija, El Khalfi, Bouchra, Barakat, Abdelhamid

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Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness by Bousfiha, Amale, Riahi, Zied, Elkhattabi, Lamiae, Bakhchane, Amina, Charoute, Hicham, Snoussi, Khalid, Bonnet, Crystel, Petit, Christine, Barakat, Abdelhamid

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Involvement of Non-synonymous Polymorphisms of the HNF1A Gene in Susceptibility to Metabolic Syndrome: Association Study and Molecular Dynamics by Elkhattabi, Lamiae E., Morjane, Imane, Charoute, Hicham, Kettani, Anas, Saile, Rachid, Barakat, Abdelhamid

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