Analysis of genetic variations of bone formation signaling pathways in patents of osteoarthritis.
Association of HMGA1 gene polymorphism(s) with type 2 diabetes mellitus
Association of TNF polymorphism with autoimmune diseases
Characterization of HCV infection in diabetic patients in Pakistan
Detection of Apolipoprotein E polymorphism in Coronary Heart Disease.
Epigenetic and Genetic Analysis of Cell Signaling Pathway Genes in Squamous Cell Carcinomas
Genetic Alteration(s) in Oral Submucous Fibrosis (OSF) are Associated with Oral Squamous Cell Carcinoma (OSCC): Relationship with TP53 and its Regulator Genes
Genetic analyses of FTO gene in diabetes and its complications
Genetic analysis of leishmaniasis in Pakistani population
Genetic identification of rare congenital skin disorders
Genetic mutations in diabetes and its complications e.g: hypertension and nephropathy
Genetic polymorphism in Haptoglobin gene in diabetes and nephropathy
Genetic Variation(s) in the Genes of p53 Pathway Regulators: An Association with the Susceptibility to Breast Cancer in Pakistan
Glutathione-S- Transferases (GSTM1 andGSTT1) and Cytochrome P450 (CYP1A1) gene polymorphism and acute lymphoblastic leukemia (ALL)
Identification of genetic variants of HBV and HDV in Pakistan
Inherited and acquired p53 mutation: their relationship with anti p53 antibodies patients potentially malignant and malignant patients with oral cavity cancer
Molecular epidemiology and antimicrobial resistance of Staphylococcus Aureus.
Multilocus sequence typing of methicillin resistant and sensitive Staphylococcus Aureus
Study of Antiplatelet Effect and Lipoxygenase Inhibition of Bergenin on Human Blood
Subtyping and antibiotyping of methicillin resistant Staphylococcus Aureus
Variations in genes associated with vitamin D and Their possible correlation with diabetes and its complications
Vitamin D status and its relationship to the risk and pathogenesis of cardiovascular disease in Fako division, Cameroon.
