Domaine de Maîtrise :
Biopathologie et Recherche Biomédicale

Domaine d’intérêt :
Épidémiologie et Santé Publique, Biopathologie et Recherche Biomédicale**

Les publications :
1. Najar, M., et al., Empowering the immune fate of bone marrow mesenchymal stromal cells: gene and protein changes. Inflammation research, 2019. 68(2): p. 167-176. 2. Najar, M., et al., Mesenchymal Stromal Cell-Based Therapy: New Perspectives and Challenges. 2019, Multidisciplinary Digital Publishing Institute. 3. Bouhtit, F., et al., The biological response of mesenchymal stromal cells to thymol and carvacrol in comparison to their essential oil: An innovative new study. Food and Chemical Toxicology, 2019: p. 110844. 4. Hardi, H., et al., Significant association between ERCC2 and MTHR polymorphisms and breast cancer susceptibility in Moroccan population: genotype and haplotype analysis in a case-control study. BMC cancer, 2018. 18(1): p. 292. 5. Garchon, H.J., et al., CYP1B1 mutations in French patients with early–onset primary open–angle glaucoma. Investigative Ophthalmology & Visual Science, 2004. 45(13): p. 4624-4624. 6. El Akil, S., R. Melki, and A. Belmouden, Genetic heterogeneity in Moroccan primary congenital glaucoma patients. Life Sci J, 2014. 11(11): p. 890-898. 7. Melki, R., et al., The M98K variant of the OPTINEURIN (OPTN) gene modifies initial intraocular pressure in patients with primary open angle glaucoma. Journal of medical genetics, 2003. 40(11): p. 842-844. 8. Melki, R., et al., Myocilin analysis by DHPLC in French POAG patients: increased prevalence of Q368X mutation. Human mutation, 2003. 22(2): p. 179-179. 9. Melki, R., et al., CYP1B1 mutations in French patients with early-onset primary open-angle glaucoma. Journal of medical genetics, 2004. 41(9): p. 647-651. 10. Melki, R., et al., Functional analysis of the MHC-linked Idd16 locus for type 1 diabetes in non-obese diabetic (NOD) mice. Tissue Antigens, 2006. 67(6). 11. Melki, R., et al., Mutational analysis of the Myocilin gene in patients with primary open-angle glaucoma in Morocco. Ophthalmic genetics, 2003. 24(3): p. 153-160. 12. Melki, R., et al., Association of a common coding polymorphism (N453S) of the cytochrome P450 1B1 (CYP1B1) gene with optic disc cupping and visual field alteration in French patients with primary open-angle glaucoma. Mol Vis, 2005. 11: p. 1012-7. 13. Boudouaya, H., et al., Prevalence of Legionella species in hot water of Moorish baths “Hammams” and domestic bathrooms in Oujda city, Morocco. 2017. 14. Belmouden, A., et al., A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco. Clinical genetics, 2002. 62(4): p. 334-339. 15. Rocha-Campos, A.-C., et al., Genetic and functional analysis of the Nkt1 locus using congenic NOD mice: improved Vα14-NKT cell performance but failure to protect against type 1 diabetes. Diabetes, 2006. 55(4): p. 1163-1170.