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Currently used diagnostic biomarker methods, such as cerebrospinal fluid (CSF) analysis and positron emission tomography (PET) imaging, provide valuable information but are invasive, expensive and not suitable as a front-line screener 5,7

Therefore, our objective was to explore the interplay between two key players in BD disease pathophysiology: mitochondrial dysfunction and inflammation

NAD + homeostasis in health and disease

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cells were labeled with CM-H 2 DCFDA and stained with acridine orange-ethidium bromide (AO/EB) and Nuc-blue

Excitation at either maxima results in emission at 510 nm