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Neuropathology and Applied Neurobiology|July 5, 2001
Ubiquitin C-terminal hydrolase-L1 (PGP9.5) expression in human neural cell lines following induction of neuronal differentiation and exposure to cytokines, neurotrophic factors or heat stressJ I Satoh, Y Kuroda
Neuropathology and Applied Neurobiology|July 5, 2001
Mutational analysis of TSC1 and TSC2 genes in gangliogliomasA J Becker, M Löbach, H Klein, et al.
Neuropathology and Applied Neurobiology|July 31, 2003
Glycohistochemical characterization of vascular muscle cell destruction in CADASIL subjects by lectins, neoglycoconjugates and galectin-specific antibodiesP Brulin-Fardoux, C Godfrain, C-A Maurage, et al.
Neuropathology and Applied Neurobiology|February 1, 1992
Age-related ubiquitin deposits in dystrophic neurites: an immunoelectron microscopic studyA Migheli, A Attanasio, T Pezzulo, et al.
Neuropathology and Applied Neurobiology|June 6, 2003
APOE epsilon 4 influences the pathological phenotype of Alzheimer's disease by favouring cerebrovascular over parenchymal accumulation of A beta proteinK Chalmers, G K Wilcock, S Love
Neuropathology and Applied Neurobiology|June 6, 2003
Frontotemporal and motor neurone degeneration with neurofilament inclusion bodies: additional evidence for overlap between FTD and ALSE H Bigio, A M Lipton, C L White, et al.
Neuropathology and Applied Neurobiology|June 6, 2003
Alpha-synuclein-positive structures in association with diffuse neurofibrillary tangles with calcificationN Hishikawa, Y Hashizume, N Ujihira, et al.
Neuropathology and Applied Neurobiology|November 27, 2021
AKT1E17K -mutated meningioma cell lines respond to treatment with the AKT inhibitor AZD5363Peter John, Natalie Waldt, Josephine Liebich, et al.
Neuropathology and Applied Neurobiology|September 10, 2019
Neuropathological characterization of a novel TANK binding kinase (TBK1) gene loss of function mutation associated with amyotrophic lateral sclerosisM Weinreich, S R Shepheard, N Verber, et al.
Neuropathology and Applied Neurobiology|February 3, 2021
A rare case of paediatric astroblastoma with concomitant MN1-GTSE1 and EWSR1-PATZ1 gene fusions altering managementKaran R Chadda, Katherine Holland, Daniel Scoffings, et al.
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