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Human Genetics|June 17, 2015
High diagnostic yield of clinical exome sequencing in Middle Eastern patients with Mendelian disordersTarunashree Yavarna, Nader Al-Dewik, Mariam Al-Mureikhi, et al.
International Journal of Molecular Sciences|September 9, 2022
Gene Expression Landscape of Chronic Myeloid Leukemia K562 Cells Overexpressing the Tumor Suppressor Gene PTPRGGiulia Lombardi, Roberta Valeria Latorre, Alessandro Mosca, et al.
Endocrine, Metabolic & Immune Disorders Drug Targets|May 1, 2019
Diabetes-induced Proteome Changes Throughout DevelopmentDina Johar, Sara M Ahmed, Samer El Hayek, et al.
Blood|October 22, 2015
Clinical and molecular response to interferon-α therapy in essential thrombocythemia patients with CALR mutationsEmmanuelle Verger, Bruno Cassinat, Aurélie Chauveau, et al.
Lifestyle Genomics|January 2, 2025
Exploring Differentially Methylated Genes among Preterm Birth and Full-Term BirthAleem Razzaq, Razan ElKahlout, Gheyath K Nasrallah, et al.
Human Mutation|November 9, 2018
In silico and in vivo models for Qatari-specific classical homocystinuria as basis for development of novel therapiesHesham M Ismail, Navaneethakrishnan Krishnamoorthy, Nader Al-Dewik, et al.
BMC Gastroenterology|June 16, 2021
The prevalence of HEV among non-A-C hepatitis in Qatar and efficiency of serological markers for the diagnosis of hepatitis EEnas S Al Absi, Duaa W Al-Sadeq, Makiyeh Khalili, et al.
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