[HTML][HTML] Step by step: towards a better understanding of the genetic architecture of Alzheimer's disease

JC Lambert, A Ramirez, B Grenier-Boley… - Molecular …, 2023 - nature.com
Alzheimer's disease (AD) is considered to have a large genetic component. Our knowledge
of this component has progressed over the last 10 years, thanks notably to the advent of …

[HTML][HTML] The genetic architecture of Alzheimer's disease: beyond APP, PSENs and APOE

RJ Guerreiro, DR Gustafson, J Hardy - Neurobiology of aging, 2012 - Elsevier
Alzheimer's disease (AD) is a complex disorder with a clear genetic component. Three
genes have been identified as the cause of early onset familial AD (EOAD). The most …

[图书][B] Testing statistical hypotheses of equivalence

S Wellek - 2002 - taylorfrancis.com
Equivalence testing has grown significantly in importance over the last two decades,
especially as its relevance to a variety of applications has become understood. Yet …

Apolipoprotein E4 effects in Alzheimer's disease are mediated by synaptotoxic oligomeric amyloid-β

RM Koffie, T Hashimoto, HC Tai, KR Kay… - Brain, 2012 - academic.oup.com
The apolipoprotein E ε4 gene is the most important genetic risk factor for sporadic
Alzheimer's disease, but the link between this gene and neurodegeneration remains …

Causative and susceptibility genes for Alzheimer's disease: a review

A Rocchi, S Pellegrini, G Siciliano, L Murri - Brain research bulletin, 2003 - Elsevier
Alzheimer's disease (AD) is the most common type of dementia in the elderly population.
Three genes have been identified as responsible for the rare early-onset familial form of the …

Transcriptional regulation of BACE1, the β-amyloid precursor protein β-secretase, by Sp1

MA Christensen, W Zhou, H Qing… - … and cellular biology, 2004 - Taylor & Francis
Proteolytic processing of the β-amyloid precursor protein (APP) at the β site is essential to
generate Aβ. BACE1, the major β-secretase involved in cleaving APP, has been identified …

Apolipoprotein Eε4 modifies Alzheimer's disease onset in an E280A PS1 kindred

P Pastor, CM Roe, A Villegas, G Bedoya… - Annals of …, 2003 - Wiley Online Library
We previously have identified a large kindred from Colombia in which Alzheimer's disease
(AD) is caused by the E280A presenilin 1 (PS1) mutation. The objective of this study was to …

Cholinergic‐associated loss of hnRNP‐A/B in Alzheimer's disease impairs cortical splicing and cognitive function in mice

A Berson, S Barbash, G Shaltiel, Y Goll… - EMBO molecular …, 2012 - embopress.org
Genetic studies link inherited errors in RNA metabolism to familial neurodegenerative
disease. Here, we report such errors and the underlying mechanism in sporadic Alzheimer's …

Genetics of Alzheimer's disease: new evidences for an old hypothesis?

JC Lambert, P Amouyel - Current opinion in genetics & development, 2011 - Elsevier
Alzheimer's disease (AD) is the prime cause of dementia and presents a strong genetic
predisposition (60–80% of the attributable risk). In addition to APOE, a major recognized …

[HTML][HTML] Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker …

CE Yu, H Seltman, ER Peskind, N Galloway, PX Zhou… - Genomics, 2007 - Elsevier
The ε4 allele of APOE confers a two-to fourfold increased risk for late-onset Alzheimer's
disease (LOAD), but LOAD pathology does not all fit neatly around APOE. It is conceivable …