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Now showing items 11-20 of 29
Effects of ATP, Mg2+, and redox agents on the Ca2+ dependence of RyR channels from rat brain cortex
(AMER PHYSIOLOGICAL SOC, 2007-07)
Association of Parkinson disease to PARK16 in a Chilean sample
(Elsevier, 2011-01)
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin
(WILEY-LISS, DIV JOHN WILEY & SONS, 2006-09)
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
(NATURE PUBLISHING GROUP, 2006-10)
Neuropathologic Heterogeneity in HDDD1: A Familial Frontotemporal Lobar Degeneration With Ubiquitin-positive Inclusions and Progranulin Mutation
(Lippincott Williams & Wilkins, 2007-03)