Intracellular fluorescent tracers are useful tools to identify adoptively transferred T cells.

Injections of fluorescent tracers and BDA into particular temporal areas were made in eleven dogs.

Microscopic analysis of the pathological inclusions revealed that the fluorescent tracers preferentially bind to premature tau aggregates.

In order to define the projections of the particular areas, injections of fluorescent tracers were made in three monkeys.

Utilizing retrograding lumafluor fluorescent tracers and electrophysiology techniques, we performed cell type- and circuit-specific measures of neuronal firing rates.

In three additional animals, combined injections of fluorescent tracers along the HM representation in V1 yielded two projection sites at the anterior border of V2.