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Tissue sections were blocked with 3% goat serum for 60 minutes at room temperature, stained with an antibody cocktail solution (containing 750 g/mL of each antibody) at 4C for 15 hours, washed with 0.2 % Triton X-100 in PBS for 8 minutes, and then stained with nuclear Intercalator-Ir (Fluidigm) at 300 L/section

[599] underscore the need for large-scale targeted mechanistic studies, such as longitudinal gut-microbiome profiling, in vivo models of -synuclein propagation, and integrated immunemetabolite analyses, to elucidate pathways along the gutbrain axis

Common genetic variation in CYP1B1 is associated with concentrations of T, FT and FT in the sera of polycystic ovary syndrome patients

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Neurotrophic effects of taurine on spiral ganglion neurons in vitro