Lamiae Elkhattabi

Casablanca, Morocco

Last Updated: 09/26/2026

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Found 13 publications

Structure-based virtual screening to identify hypocholesterolemic phytochemicals as potent inhibitors of squalene synthase a potential target for hypercholesterolemia.

Structure-based virtual screening to identify hypocholesterolemic phytochemicals as potent inhibitors of squalene synthase a potential target for hypercholesterolemia.

Journal: Journal of biomolecular structure & dynamics

Published: December 03, 2024

Insights from the SNP analysis of TYMP gene linking MNGIE.

Insights from the SNP analysis of TYMP gene linking MNGIE.

Journal: Bioinformation

Published: March 01, 2024

Molecular docking analysis of PPARγ with phytochemicals from Moroccan medicinal plants.

Molecular docking analysis of PPARγ with phytochemicals from Moroccan medicinal plants.

Journal: Bioinformation

Published: July 01, 2023

Computational screening of potential drugs against COVID-19 disease: the Neuropilin-1 receptor as molecular target.

Computational screening of potential drugs against COVID-19 disease: the Neuropilin-1 receptor as molecular target.

Journal: Virusdisease

Published: April 24, 2021

Potential inhibitors of SARS-cov-2 RNA dependent RNA polymerase protein: molecular docking, molecular dynamics simulations and MM-PBSA analyses.

Potential inhibitors of SARS-cov-2 RNA dependent RNA polymerase protein: molecular docking, molecular dynamics simulations and MM-PBSA analyses.

Journal: Journal of biomolecular structure & dynamics

Published: September 03, 2020

Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family.

Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family.

Journal: Human heredity

Published: August 30, 2020

Omenn syndrome caused by a novel homozygous mutation in recombination activating gene 1.

Omenn syndrome caused by a novel homozygous mutation in recombination activating gene 1.

Journal: Immunobiology

Published: July 21, 2020

Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness.

Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness.

Journal: Human heredity

Published: July 02, 2019

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.

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.

Journal: Cardiology research and practice

Published: June 25, 2019

Computational Analysis of nsSNPs of ADA Gene in Severe Combined Immunodeficiency Using Molecular Modeling and Dynamics Simulation.

Computational Analysis of nsSNPs of ADA Gene in Severe Combined Immunodeficiency Using Molecular Modeling and Dynamics Simulation.

Journal: Journal of immunology research

Published: May 23, 2019

Chromosomal Abnormalities in Patients with Intellectual Disability: A 21-Year Retrospective Study.

Chromosomal Abnormalities in Patients with Intellectual Disability: A 21-Year Retrospective Study.

Journal: Human heredity

Published: October 29, 2018

In Silico Analysis of Coding/Noncoding SNPs of Human RETN Gene and Characterization of Their Impact on Resistin Stability and Structure.

In Silico Analysis of Coding/Noncoding SNPs of Human RETN Gene and Characterization of Their Impact on Resistin Stability and Structure.

Journal: Journal of diabetes research

Published: October 26, 2018

Showing 1-12 of 13

Last Updated: 09/26/2026