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Genetics and Molecular Biology|April 2, 2014
Genetic diversity and prevalence of CCR2-CCR5 gene polymorphisms in the Omani populationSamira H Al-Mahruqi, Fahad Zadjali, Albano Beja-Pereira, et al.Hormone Molecular Biology and Clinical Investigation|May 12, 2015
Liver X receptor agonist downregulates growth hormone signaling in the liverFahad Zadjali, Ruyman Santana-Farre, Mercedes Mirecki-Garrido, et al.International Journal of Molecular Sciences|March 7, 2020
Tuberous Sclerosis Complex Axis Controls Renal Extracellular Vesicle Production and Protein ContentFahad Zadjali, Prashant Kumar, Ying Yao, et al.Current Pharmaceutical Biotechnology|April 2, 2016
Nutraceuticals as Lipid-Lowering Treatment in Pregnancy and Their Effects on the Metabolic SyndromeTamima Al-Dughaishi, Dragana Nikolic, Fahad Zadjali, et al.Oncotarget|October 28, 2016
Stimulation of prolactin receptor induces STAT-5 phosphorylation and cellular invasion in glioblastoma multiformeAmira Alkharusi, Shengze Yu, Natalia Landázuri, et al.Human Biology|December 14, 2007
N-acetyltransferase polymorphism among northern SudaneseSaid Al-Yahyaee, Uzma Gaffar, Maryam M Al-Ameri, et al.Human Mutation|July 18, 2018
Homozygosity for FARSB mutation leads to Phe-tRNA synthetase-related disease of growth restriction, brain calcification, and interstitial lung diseaseFahad Zadjali, Aida Al-Yahyaee, Maryam Al-Nabhani, et al.Sultan Qaboos University Medical Journal|June 8, 2022
Socio-Demographic and Clinical Profiles of Adult Attention Deficit Hyperactivity Disorder Patients in a University Hospital in OmanHassan Mirza, Salim Al-Huseini, Shamsa Al-Jamoodi, et al.Movement Disorders Clinical Practice|November 12, 2021
Biallelic <i>PTRHD1</i> Frameshift Variants Associated with Intellectual Disability, Spasticity, and ParkinsonismGhalia Al-Kasbi, Abeer Al-Saegh, Ahmed Al-Qassabi, et al.Genes & Diseases|January 10, 2022
<i>Tsc2</i> mutation induces renal tubular cell nonautonomous diseasePrashant Kumar, Fahad Zadjali, Ying Yao, et al.Pageof 6