GENE XRCC1ARG399GLN POLYMORPHISM AND ITS GENOTYPE VARIATIONS: CLINICAL ASSOCIATIONS IN EGYPTIAN SYSTEMIC LUPUS ERYTHEMATOSUS PATIENTS

Gene XRCC1Arg399Gln polymorphism and its genotype variations: clinical associations in Egyptian systemic lupus erythematosus patients

Abstract Background joint care Impaired deoxyribonucleic acid (DNA) repair may induce an autoimmune response in susceptible individuals.The association between DNA repair gene XRCC1 Arg399Gln gene polymorphism and susceptibility of systemic lupus erythematosus (SLE) is controversial.This study aimed to detect the association of XRCC1 Arg399Gln gene

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Subgraph Query for Building Service-Based Systems

Given the broad applications of service-oriented architecture (SOA) in service-oriented software engineering, service-based systems (SBSs) built from existing Web services are becoming Calendula increasingly popular.As a result, the selection of the appropriate component services to include in SBSs has become a crucial step in the SBS-engineering p

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Multimodal imaging features of a spontaneously resolved unilateral congenital macrovessel-related macular edema in a 13-year-old boy

Purpose: Congenital retinal macrovessels (CRM) are large aberrant blood vessels that cross the Ski de fond - Equipement - Skis - Pieces de rechange horizontal raphe.Visual acuity may be negatively affected in cases afflicted with CRM due to macular serous detachment, hemorrhage, exudation, foveolar cyst formation and retinal artery occlusion.Even t

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