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International Journal of Environmental Research and Public Health|April 21, 2017
Evaluation of the Effects of Airborne Particulate Matter on Bone Marrow-Mesenchymal Stem Cells (BM-MSCs): Cellular, Molecular and Systems Biological ApproachesMuhammad Abu-Elmagd, Mansour A Alghamdi, Magdy Shamy, et al.
BMC Cancer|February 25, 2015
pecific nutrient combination effects on tax, NF- κB and MMP-9 in human T-cell lymphotropic virus -1 positive malignant T-lymphocytesSteve Harakeh, Rania Azar, Esam Azhar, et al.
BMC Medical Genetics|October 22, 2016
Identification of novel genetic variations affecting osteoarthritis patientsMamdooh Abdullah Gari, Mohammed AlKaff, Haneen S Alsehli, et al.
Frontiers in Molecular Biosciences|March 3, 2022
The Prognostic Value of the Developmental Gene FZD6 in Young Saudi Breast Cancer Patients: A Biomarkers Discovery and Cancer Inducers OncoScreen ApproachMourad Assidi, Abdelbaset Buhmeida, Maryam H Al-Zahrani, et al.
Genes|April 23, 2022
Utility of Circulating Cell-Free DNA in Assessing Microsatellite Instability and Loss of Heterozygosity in Breast Cancer Using Human Identification ApproachNorah A Al Sharhan, Safia A Messaoudi, Saranya R Babu, et al.
BMC Medical Genetics|October 22, 2016
Associations of recurrent miscarriages with chromosomal abnormalities, thrombophilia allelic polymorphisms and/or consanguinity in Saudi ArabiaRola F Turki, Mourad Assidi, Huda A Banni, et al.
The Libyan Journal of Medicine|November 1, 2021
Prognostic value of E-Cadherin and its tumor suppressor role in Saudi women with advanced epithelial ovarian cancerMourad Assidi, Mohammad Alam Jafri, Muhammad Abu-Elmagd, et al.
BMC Genomics|October 22, 2016
The Third International Genomic Medicine Conference (3rd IGMC, 2015): overall activities and outcome highlightsMuhammad Abu-Elmagd, Mourad Assidi, Ashraf Dallol, et al.
Arthritis and Rheumatism|December 7, 2011
The expression and function of microRNAs in chondrogenesis and osteoarthritisTracey E Swingler, Guy Wheeler, Virginia Carmont, et al.
BMC Genomics|April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M SyndromeChristian R Marshall, Sandra A Farrell, Donna Cushing, et al.
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