Apolipoprotein E alleles as risk factors in Alzheimer's disease

AD Roses, MD - Annual review of medicine, 1996 - annualreviews.org
▪ Abstract Alzheimer's disease (AD) is unique in medicine in that millions of people suffer
from what appears to be the same form of disease, and unlike most other late-onset …

The role of cerebral amyloid β accumulation in common forms of Alzheimer disease

S Gandy - The Journal of clinical investigation, 2005 - Am Soc Clin Investig
For approximately 80 years following Alzheimer's description of the disease that bears his
name, a gulf divided researchers who believed that extracellular deposits of the amyloid β …

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

R Sherrington, EI Rogaev, Y Liang, EA Rogaeva… - Nature, 1995 - nature.com
Some cases of Alzheimer's disease are inherited as an autosomal dominant trait. Genetic
linkage studies have mapped a locus (AD3) associated with susceptibility to a very …

Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes

G Jun, AC Naj, GW Beecham, LS Wang… - Archives of …, 2010 - jamanetwork.com
Objectives: To determine whether genotypes at CLU, PICALM, and CR1 confer risk for
Alzheimer disease (AD) and whether risk for AD associated with these genes is influenced …

A familial Alzheimer's disease locus on chromosome 1

E Levy-Lahad, EM Wijsman, E Nemens, L Anderson… - Science, 1995 - science.org
The Volga German kindreds are a group of seven related families with autosomal dominant
early-onset Alzheimer's disease (AD). Linkage to known AD-related loci on chromosomes …

Apolipoprotein E, dementia, and cortical deposition of β-amyloid protein

T Polvikoski, R Sulkava, M Haltia… - … England Journal of …, 1995 - Mass Medical Soc
Background The ε4 allele of apolipoprotein E has been associated with an increased risk of
late-onset Alzheimer's disease. In a cohort of elderly subjects we prospectively investigated …

Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant

R Sherrington, S Froelich, S Sorbi… - Human molecular …, 1996 - academic.oup.com
Missense mutations in the presenilin 2 (PS-2) gene on chromosome 1 were sought by direct
nucleotide sequence analysis of the open reading frame of 60 pedigrees with familial …

The genetics and neuropathology of Alzheimer's disease

GD Schellenberg, TJ Montine - Acta neuropathologica, 2012 - Springer
Here we review the genetic causes and risks for Alzheimer's disease (AD). Early work
identified mutations in three genes that cause AD: APP, PSEN1 and PSEN2. Although …

Behavioral and anatomical deficits in mice homozygous for a modified β-amyloid precursor protein gene

U Müller, N Cristina, ZW Li, DP Wolfer, HP Lipp… - Cell, 1994 - cell.com
The p-amyloid precursor protein (pAPP) gene of the mouse was disrupted by inserting into
exon 2 a cassette containing a neomycin resistance gene and a putative transcription …

Molecular genetics of Alzheimer's disease

PH St George-Hyslop - Biological psychiatry, 2000 - Elsevier
Application of genetic paradigms to Alzheimer's disease (AD) has led to confirmation that
genetic factors play a role in this disease. Additionally, researchers now understand that AD …