Publications by authors named "Ghazi Alghanim"

Article Synopsis
  • * A total of 1,025 individuals vaccinated with BNT162b2 or ChAdOx1 were analyzed, revealing that those with prior infections had significantly higher antibody levels compared to those without.
  • * The findings suggest that prior infections contribute to more durable antibody responses following vaccination, indicating the need for focused vaccination efforts, especially for individuals without previous infections amidst global vaccine shortages.
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The family of angiopoietin-like proteins (ANGPTLs) is composed of eight ANGPTLs members that are involved in regulating various metabolic processes and have been implicated in type 2 diabetes (T2D) and obesity. ANGPTL5 is an understudied member of this family that has been suggested to regulate triglyceride metabolism with a potential role in obesity. This study was designed to investigate the expression levels of ANGPTL5 protein in the circulation of subjects with obesity and T2D.

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Article Synopsis
  • The article DOI: 10.3389/fgene.2018.00689 has been updated or corrected to address previous inaccuracies.
  • This correction ensures the integrity and accuracy of the research published in that article.
  • Readers should refer to the corrected version for the most reliable information.
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Caveolin-1 () variants have been suggested to be associated with obesity and related metabolic disorders, but information based on human studies is limited. In the present study, we aimed to investigate the potential association between the rs1997623 C/A variant and metabolic syndrome (MetS) in Kuwaiti children. DNA from saliva samples collected from 1313 Kuwaiti children (mean age: 12 years) were genotyped using the TaqMan SNP genotyping assay.

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Background: Leber's hereditary optic neuropathy (LHON) is a condition characterised by a rapid bilateral central vision loss due to death of the retinal ganglion cells, leading to visual impairment commonly occurring during young adulthood. The disease manifests itself more in male patients than female patients. The mtDNA mutations m.

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