• Creative English Writing

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  • UAE Innovation Month

  • University Forum Magazine | Issue #102 - January 2018

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  • Jobs at University of Sharjah

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  • 1st International Sharjah Spring School in Mathematics

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  • Third International Forum on Innovation and Entrepreneurship

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  • Sharjah 1st International Conference for Persons with Disabilities

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  • 1st international conference of UOS branches

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Latest 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 OF, Rebai EM, Tabebi M, Tej A, Chamkha I, Tlili A, Bouguila J, Tilouche S, Soyah N, Boughamoura L, Fakhfakh F. (2015). Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in MT-ND2 and MT-TL1 genes. Mitochondrial DNA.10:1-8. 

  • Raafat A.El-Awady, Fatema Herzi, Hala Al-Tunaiji, Ekram M. Saleh, Abdel-Hady A. Abdel-Wahab, Amer Al Homssi, Mousa Suhail, Ahmed El-Serafi and Taleb Al-Tel (2015). Epigenetics and miRNA as predictive markers and targets for lung cancer chemotherapy. Cancer Biology and Therapy 7: 1056—1070

  • Mostafa Hassan and Ahmed T. El-Serafi (2015). Personalized Treatment: The Future of Medicine. A Perspective on the Preconditioning for Stem Cell Transplantation. Editorial in MOJ Cell Science and Report 2: 00032.

  • Randa M. Mstafa, Ahmed T. El-Serafi and Ayman Shafei (2015). The Stolen Dreams, Endocrine Disrupting Chemicals and Childhood Obesity. Review article in Medico Research Chronicles. 2: 564-571.

  • Hatem Sallam, Ahmed T. El Serafi, Elisabeth Filipski, Ylva Tereliusd, Francis Lévi and Moustapha Hassan (2015). The effect of circadian rhythm on pharmacokinetics and metabolism of the Cdk inhibitor, roscovitine. International Chronobiology. 32: 608-614.

  • Shymaa Maher, Eman Kolieb, Nagwan A Sabik, Dalia Abd-Elhalim, Ahmed T El-Serafi and Yasser El-Wazir (2015). Comparison of the Osteogenic Differentiation Potential of Mesenchymal Cells Isolated from Human Bone Marrow, Umbilical Cord Blood and Placenta Derived Stem Cells. Beni-Suef University Journal of Basic and Applied Sciences 4: 80-85.

  • Tlili, A., Al Mutery, A., Kamal Eddine Ahmad Mohamed, W., Mahfood, M., & Hadj Kacem, H. (2017). 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.

  • Tlili A, Fahd Al Mutery A, Mahfood M, Kamal Eddine Ahmad Mohamed W, Bajou K. (2017). 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.

  • Olfa Alila-Fersi , Imen Chamkha , Imen Majdoub , Lamia Gargouri  , Emna Mkaouar-Rebai  , Mouna Tabebi d , Abdelaziz Tlili , Leila Keskes , Abdelmajid Mahfoudh , Faiza Fakhfakh. (2017).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.

  • Mouna Tabebi, Nadia Charfi , Fakhri Kallabi, Olfa Alila-Fersi, Afif Ben Mahmoud, Abdelaziz Tlili, Leila Keskes-Ammar, Hassen Kamoun, Mohamed Abid , Mouna Mnif, Faiza Fakhfakh.(2017).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 N G mutation. Diabetes and Its Complications. 31 (1): 253–259.

  • 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.