VPS35 and frontotemporal dementia: Mice that selectively depleted Vps35 gene in embryonic (by Neurod6-Cre) pyramidal neurons display FTD-like neuropathology, including progressive reduction of cortical thickness, elevation of cortical neuronal death, accumulations of P62, LC3-II, Tdp43, and ubiquitin-conjugated protein levels, impairments in lysosomal morphology and acidification, and reactive gliosis.