Elkhattabi L - Search Results

1

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

Elkhattabi L, Morjane I, Charoute H, Amghar S, Bouafi H, Elkarhat Z, Saile R, Rouba H, Barakat A. Elkhattabi L, et al. J Diabetes Res. 2019 May 20;2019:4951627. doi: 10.1155/2019/4951627. eCollection 2019. J Diabetes Res. 2019. PMID: 31236417 Free PMC article.

2

A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family.

Salime S, Riahi Z, Elrharchi S, Elkhattabi L, Charoute H, Nahili H, Rouba H, Kabine M, Bonnet C, Petit C, Barakat A. Salime S, et al. Among authors: elkhattabi l. Gene. 2018 Jun 15;659:89-92. doi: 10.1016/j.gene.2018.03.042. Epub 2018 Mar 15. Gene. 2018. PMID: 29551497

3

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

Belkady B, Elkhattabi L, Elkarhat Z, Zarouf L, Razoki L, Aboulfaraj J, Nassereddine S, Cadi R, Rouba H, Barakat A. Belkady B, et al. Among authors: elkhattabi l. Hum Hered. 2018;83(5):274-282. doi: 10.1159/000499710. Epub 2019 May 7. Hum Hered. 2018. PMID: 31064002

4

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

Essadssi S, Krami AM, Elkhattabi L, Elkarhat Z, Amalou G, Abdelghaffar H, Rouba H, Barakat A. Essadssi S, et al. Among authors: elkhattabi l. J Immunol Res. 2019 Nov 3;2019:5902391. doi: 10.1155/2019/5902391. eCollection 2019. J Immunol Res. 2019. PMID: 31781678 Free PMC article.

5

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

Bousfiha A, Riahi Z, Elkhattabi L, Bakhchane A, Charoute H, Snoussi K, Bonnet C, Petit C, Barakat A. Bousfiha A, et al. Among authors: elkhattabi l. Hum Hered. 2019;84(3):109-116. doi: 10.1159/000503450. Epub 2019 Dec 4. Hum Hered. 2019. PMID: 31801140

6

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.

Morjane I, Charoute H, Ouatou S, Elkhattabi L, Benrahma H, Saile R, Rouba H, Barakat A. Morjane I, et al. Among authors: elkhattabi l. Cardiol Res Pract. 2020 Aug 4;2020:5981971. doi: 10.1155/2020/5981971. eCollection 2020. Cardiol Res Pract. 2020. PMID: 32832146 Free PMC article.

7

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

Elkarhat Z, Charoute H, Elkhattabi L, Barakat A, Rouba H. Elkarhat Z, et al. Among authors: elkhattabi l. J Biomol Struct Dyn. 2022 Jan;40(1):361-374. doi: 10.1080/07391102.2020.1813628. Epub 2020 Sep 2. J Biomol Struct Dyn. 2022. PMID: 32873176

8

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

Elrharchi S, Riahi Z, Salime S, Charoute H, Elkhattabi L, Boulouiz R, Kabine M, Bonnet C, Petit C, Barakat A. Elrharchi S, et al. Among authors: elkhattabi l. Hum Hered. 2020;85(1):35-39. doi: 10.1159/000512712. Epub 2021 Jan 22. Hum Hered. 2020. PMID: 33486474

9

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

Benhsaien I, Essadssi S, Elkhattabi L, Bakhchane A, Abdelghaffar H, Bousfiha AA, Badou A, Barakat A. Benhsaien I, et al. Among authors: elkhattabi l. Immunobiology. 2021 May;226(3):152090. doi: 10.1016/j.imbio.2021.152090. Epub 2021 Apr 28. Immunobiology. 2021. PMID: 33964732

10

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

Charoute H, Elkarhat Z, Elkhattabi L, El Fahime E, Oukkache N, Rouba H, Barakat A. Charoute H, et al. Among authors: elkhattabi l. Virusdisease. 2022 Mar;33(1):23-31. doi: 10.1007/s13337-021-00751-x. Epub 2022 Jan 21. Virusdisease. 2022. PMID: 35079600 Free PMC article.

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