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Publications

  • Tee Jong Huat, Amir Ali Khan, Soumya Pati, Zulkifli Mustafa, Jafri Malin Abdullah, Hasnan Jaafar. .(2014). IGF-1 enhances early differentiation of Bone Marrow Mesenchymal Stem Cell into Neural lineage. BMC Neuroscience, BMC Neurosci. 15(1):91.

 

  • Tee Jong Huat, Amir Ali Khan, Jafri Malin Abdullah, Fauziah Mohamad Idris and Hasnan Jaafar. (2015). MicroRNA expression profile of neural progenitor-like cells derived from mesenchymal stem cells under the influence of IGF-1, bFGF and EGF. Stem cell research. Int. J. Mol. Sci.  16(5), 9693-9718.

 

  • Tee Jong Huat, Amir Ali Khan, Jafri Malin Abdullah, Fauziah Mohamad Idris and Hasnan Jaafar. (2015). MicroRNA expression Profile of Bone Marrow Mesenchymal Stem Cells-derived Neural Progenitor Cells by microarray under the influence of EGF, bFGF and IGF-1. Genomics Data.  5:201–205.

 

  • Alila, Olfa Fersi; Rebai, Emna Mkaouar; Tabebi, Mouna; Tej, Amel; Chamkha, Imen; Tlili, Abdelaziz; Bouguila, Jihene; Tilouche, Samia; Soyah, Nejla; Boughamoura, Lamia; Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in MT-ND2 and MT-TL1 genes Mitochondrial DNA Part A 27, 4, 2873-2880, 2016, Taylor & Francis

 

  • Kallel-Bouattour R, Belguith-Maalej S, Zouari-Bradai E, Mnif M, Abid M, Hadj Kacem H.(2017 ). Intronic variants of SLC26A4 gene enhance splicing efficiency in hybrid minigene assay. Gene.15(620):10-14. 

 

  • Tabebi, Mouna; Charfi, Nadia; Kallabi, Fakhri; Alila-Fersi, Olfa; Mahmoud, Afif Ben; Tlili, Abdelaziz; Keskes-Ammar, Leila; Kamoun, Hassen; Abid, Mohamed; Mnif, Mouna; Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m. 8241 T> G mutation Journal of Diabetes and its Complications 31, 1, 253-259, 2017, Elsevier

 

  • Alila-Fersi, Olfa; Chamkha, Imen; Majdoub, Imen; Gargouri, Lamia; Mkaouar-Rebai, Emna; Tabebi, Mouna; Tlili, Abdelaziz; Keskes, Leila; Mahfoudh, Abdelmajid; Fakhfakh, Faiza; Co segregation of the m. 1555A> G mutation in the MT-RNR1 gene and mutations in MT-ATP6 gene in a family with dilated mitochondrial cardiomyopathy and hearing loss: A whole mitochondrial genome screening Biochemical and biophysical research communications, 484, 1, 71-78, 2017, Elsevier

 

  • Tlili, Abdelaziz; Fahd Al Mutery, Abdullah; Mahfood, Mona; Kamal Eddine Ahmad Mohamed, Walaa; Bajou, Khalid; Identification of a novel frameshift mutation in the ILDR1 gene in a UAE family, mutations review and phenotype genotype correlation, PloS one, 12, 9, e0185281, 2017, Public Library of Science San Francisco, CA USA

 

  • Tlili, Abdelaziz; Al Mutery, Abdullah; Kamal Eddine Ahmad Mohamed, Walaa; Mahfood, Mona; Hadj Kacem, Hassen;Prevalence of GJB2 mutations in affected individuals from United Arab Emirates with autosomal recessive nonsyndromic hearing loss, Genetic testing and molecular biomarkers, 21, 11, 686-691, 2017, Mary Ann Liebert, Inc. 140 Huguenot Street, 3rd Floor New Rochelle, NY 10801 USA

 

  • Imtiaz, Ayesha; ……………………..; Tlili Abdelaziz et al.,CDC14A phosphatase is essential for hearing and male fertility in mouse and human, Human molecular genetics, 27, 5, 780-798, 2018, Oxford University Press

 

  • Dulon, Didier; Papal, Samantha; Patni, Pranav; Cortese, Matteo; Vincent, Philippe FY; Tertrais, Margot; Emptoz, Alice; Tlili, Abdelaziz; Bouleau, Yohan; Michel, Vincent; Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome The Journal of clinical investigation, 128, 8, 3382-3401, 2018, American Society for Clinical Investigation

 

  • Hela Gargouri and Hassen Hadj Kacem. Evaluation of alternative DNA extraction protocols for the species determination in turkey salami authentication tests. International Journal of Food Properties. 2018, VOL. 21, NO. 1, 733–745

 

  • Moalla M, Hadj Kacem F, Al-Mutery AF, Mahfood M, Mejdoub-Rekik N, Abid M, Mnif-Feki M, Hadj Kacem H. Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadism. J Assist Reprod Genet. 2019 May 9. doi: 10.1007/s10815-019-01468-z.

 

  • Mahfood, Mona; Kamal Eddine Ahmad Mohamed, Walaa; Al Mutery, Abdullah; Tlili, Abdelaziz; Clinical Exome Sequencing Identifies a Frameshift Mutation Within the STRC Gene in a United Arab Emirates Family with Profound Nonsyndromic Hearing Loss, Genetic testing and molecular biomarkers, 23, 3, 204-208, 2019, Mary Ann Liebert

 

  • Abi Zamer, Batoul; Mahfood, Mona; Saleh, Batoul; Al Mutery, Abdullah Fahd; Tlili, Abdelaziz; Novel mutation in the DSG1 gene causes autosomal‐dominant striate palmoplantar keratoderma in a large Syrian family, Annals of human genetics, 83, 6, 472-476, 2019


  • Mohamed, Walaa Kamal Eldin; Mahfood, Mona; Al Mutery, Abdullah; Abdallah, Sallam Hasan; Tlili, Abdelaziz; A Novel Nonsense Mutation (c. 414G> A; p. Trp138*) in CLDN14 Causes Hearing Loss in Yemeni Families: A Case Report, Frontiers in genetics, 10, 1087, 2019, Frontiers

 

  • Abeer Maher Fayyad,Amir Ali Khan, Sallam Hasan Abdallah, Sara Sultan Alomran, Khalid Bajou and Muhammad Nasir Khan Khattak. osiglitazone Enhances Browning Adipocytes in Association with MAPK and PI3-K Pathways During the Differentiation of Telomerase-Transformed Mesenchymal Stromal Cells into Adipocytes.(2019). Int. J. Mol. Sci. (2019), 20(7), 1618.

 

  • El-Serafi AT, Sandeep D, Abdallah S, Lozansson Y,  Hamad M, Khan AA. Paradoxical effects of the epigenetic modifiers 5-aza-deoxycytidine and suberoylanilide hydroxamic acid on adipogenesis. Differentiation. (2019). 106:1-8.

 

  • Elgamouz, A., Alsaidi, R., Alsaidi, A., Zahri, M., Almehdi, A., Bajou, K. The Effects of Storage on Quality and Nutritional Values of Ehrenberg's Snapper Muscles (Lutjanus Ehrenbergi): Evaluation of Natural Antioxidants Effect on the Denaturation of Proteins.Biomolecules 2019, 9, 442; doi:10.3390/biom9090442

 

  • Chouchen, Jihen; Tlili, Abdelaziz; Two new mutations, ESPN c. 2257T> C and ESRRB c. 10583 C> A, cause hearing loss in UAE families. Hamdan Medical Journal, 13, 2, 115, 2020, Medknow Publications

 

  • Harati, Rania; Mohammad, Mohammad G; Tlili, Abdelaziz; El-Awady, Raafat A; Hamoudi, Rifat; Loss of miR-101-3p Promotes Transmigration of Metastatic Breast Cancer Cells through the Brain Endothelium by Inducing COX-2/MMP1 Signaling. Pharmaceuticals, 13, 7, 144, 2020 Multidisciplinary Digital Publishing Institute

 

  • Mohamed, Walaa Kamal Eldin; Arnoux, Marc; Cardoso, Thyago HS; Almutery, Abdullah; Tlili, Abdelaziz; Mitochondrial mutations in non-syndromic hearing loss at UAE International Journal of Pediatric Otorhinolaryngology, 138, 110286, 2020, Elsevier

 

  • Harati, Rania; Hafezi, Shirin; Mabondzo, Aloïse; Tlili, Abdelaziz;Silencing miR-202-3p increases MMP-1 and promotes a brain invasive phenotype in metastatic breast cancer cells. PloS one, 15, 10, e0239292, 2020, Public Library of Science San Francisco, CA USA

 

  • Yousef, Zamzam; Mahfood, Mona; Chouchen, Jihen; Al Mutery, Abdullah; Tlili, Abdelaziz; Identification of a novel OXCT1 frameshift mutation by whole-exome sequencing and evidence for nonsense-mediated mRNA decay. Hamdan Medical Journal, 13, 4, 222, 2020. Medknow Publications

 

  • Mehvesh Hameed, Seema Panicker, Sallam Hasan Abdallah, Amir A Khan, Changseok Han, Mohamed Chehimi, Ahmed A Mohamed. Protein-Coated Aryl Modified Gold Nanoparticles for Cellular Uptake Study by Osteosarcoma Cancer Cells. Langamiur. 2020, 33, 11765–11775.

 

  • Elgamouz, A., Alsaidi, R., Alsaidi, A., Zahri, M., Almehdi, A., Bajou, K. Dataset in the characterization of black spot Ehrenberg snapper and its proteins' denaturation inhibition by natural antioxidants. Data Brief. 2019 Dec 5;28:104927. doi: 10.1016/j.dib.2019.104927. eCollection 2020 Feb

 

  • Elgamouz, A., Idriss, H., Nassab, C., Bihi, A., Bajou, K., Hasan, K., Abu Haija, M., Patole, S.P. Green Synthesis, Characterization, Antimicrobial, Anti-Cancer, and Optimization of Colorimetric Sensing of Hydrogen Peroxide of Algae Extract Capped Silver Nanoparticles. Nanomaterials. 2020 Sep 17;10(9):E1861. doi: 10.3390/nano10091861

 

  • Khan AA, Huat TJ, Al Mutery A, El-Serafi AT, Kacem HH, Abdallah SH, Reza MF, Abdullah JM, Jaafar H, Inayat U. Significant transcriptomic changes are associated with differentiation of bone marrow-derived mesenchymal stem cells into neural progenitor-like cells in the presence of bFGF and EGF. Cell Biosci. 2020 Oct 28;10:126. doi: 10.1186/s13578-020-00487-z. PMID: 33133516; PMCID: PMC7594431.

 

  • Muhammad Nasir Khan Khattak, Abdallah Shanableh, Muhammad Iftikhar Hussain, Amir Ali Khan, Muhammad Abdulwahab, Wameed Radeef, Mohammad Harb Samreen. Anticancer activities of selected Emirati Date (Phoenix dactylifera L.) varieties pits in human triple negative breast cancer MDA-MB-231 cells. Saudi Journal of Biological Sciences. 2020, Volume 27, Issue 12, December 2020, Pages 3390-3396

 

  • Elgamouz, A., Bajou, K., Hafez, B., Nassab, C., Behi, A., Abu Haija M., Patole Optical, S.P. Sensing of Hydrogen Peroxide Using Starch Capped Silver Nanoparticles, Synthesis, Optimization and Detection in Urine. Sensors and Actuators Reports (2020), doi: https://doi.org/10.1016/j.snr.2020.100014

 

  • Fatma Mousa AlGhalban, Amir Ali Khan, and Muhammad Nasir Khan Khattak: Comparative anticancer activities of Ficus carica and Ficus salicifolia latex in MDA-MB-231 cells. Saudi Journal of Biological Sciences, 24 February 2021

 

  • Chouchen, Jihen; Mahfood, Mona; Alobathani, Maryam; Mohamed, Walaa Kamal Eldin; Tlili, Abdelaziz. Clinical heterogeneity of the SLC26A4 gene in UAE patients with hearing loss and bioinformatics investigation of DFNB4/Pendred syndrome missense mutations. International Journal of Pediatric Otorhinolaryngology, 140, 110467, 2021, Elsevier

 

  • Souissi, Amal; ………. Tlili Abdelaziz et al.,. Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population Journal of Advanced Research. 2021, Elsevier

 

  • Bashair M. Mussa, Amir Ali Khan, Ankita Srivastava and Sallam Hasan Abdallah: Differentiated PDGFRα-Positive Cells: A Novel In-Vitro Model for Functional Studies of Neuronal Nitric Oxide Synthase. Int. J. Mol. Sci. 2021, 22(7), 3514; https://doi.org/10.3390/ijms22073514