Inconsistencies and controversies surrounding the amyloid hypothesis of Alzheimer's disease

GP Morris, IA Clark, B Vissel - Acta neuropathologica communications, 2014 - Springer
The amyloid hypothesis has driven drug development strategies for Alzheimer's disease for
over 20 years. We review why accumulation of amyloid-beta (Aβ) oligomers is generally …

[HTML][HTML] Molecular genetics of early-onset Alzheimer's disease revisited

R Cacace, K Sleegers, C Van Broeckhoven - Alzheimer's & dementia, 2016 - Elsevier
As the discovery of the Alzheimer's disease (AD) genes, APP, PSEN1, and PSEN2, in
families with autosomal dominant early-onset AD (EOAD), gene discovery in familial EOAD …

Analysis of 138 pathogenic mutations in presenilin-1 on the in vitro production of Aβ42 and Aβ40 peptides by γ-secretase

L Sun, R Zhou, G Yang, Y Shi - Proceedings of the National …, 2017 - National Acad Sciences
A hallmark of Alzheimer's disease (AD) is the aggregation of β-amyloid peptides (Aβ) into
amyloid plaques in patient brain. Cleavage of amyloid precursor protein (APP) by the …

Tau protein hyperphosphorylation and aggregation in Alzheimer's disease and other tauopathies, and possible neuroprotective strategies

G Šimić, M Babić Leko, S Wray, C Harrington, I Delalle… - Biomolecules, 2016 - mdpi.com
Abnormal deposition of misprocessed and aggregated proteins is a common final pathway
of most neurodegenerative diseases, including Alzheimer's disease (AD). AD is …

A century of Alzheimer's disease

M Goedert, MG Spillantini - science, 2006 - science.org
One hundred years ago a small group of psychiatrists described the abnormal protein
deposits in the brain that define the most common neurodegenerative diseases. Over the …

[HTML][HTML] Twenty years of the Alzheimer's disease amyloid hypothesis: a genetic perspective

RE Tanzi, L Bertram - Cell, 2005 - cell.com
From Alois Alzheimer's description of Auguste D.'s brain in 1907 to George Glenner's
biochemical dissection of β-amyloid in 1984, the" amyloid hypothesis" of Alzheimer's …

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

M Cruts, I Gijselinck, J Van Der Zee, S Engelborghs… - Nature, 2006 - nature.com
Frontotemporal dementia (FTD) with ubiquitin-immunoreactive neuronal inclusions (both
cytoplasmic and nuclear) of unknown nature has been linked to a chromosome 17q21 …

Genetics of dementia

CT Loy, PR Schofield, AM Turner, JBJ Kwok - The Lancet, 2014 - thelancet.com
Summary 25% of all people aged 55 years and older have a family history of dementia. For
most, the family history is due to genetically complex disease, where many genetic …

Genetic insights in Alzheimer's disease

K Bettens, K Sleegers, C Van Broeckhoven - The lancet neurology, 2013 - thelancet.com
In the search for new genes in Alzheimer's disease, classic linkage-based and candidate-
gene-based association studies have been supplanted by exome sequencing, genome …

The genetic epidemiology of neurodegenerative disease

L Bertram, RE Tanzi - The Journal of clinical investigation, 2005 - Am Soc Clin Investig
Gene defects play a major role in the pathogenesis of degenerative disorders of the nervous
system. In fact, it has been the very knowledge gained from genetic studies that has allowed …