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The genetics and neuropathology of Alzheimer's disease
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PubMed
title
The genetics and neuropathology of Alzheimer's disease
(English)
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main subject
Alzheimer's disease
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based on heuristic
inferred from title
author name string
Gerard D. Schellenberg
series ordinal
1
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Crossref
Thomas J. Montine
series ordinal
2
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stated in
Crossref
language of work or name
English
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stated in
PubMed
publication date
September 2012
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stated in
PubMed
published in
Acta Neuropathologica
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stated in
PubMed
volume
124
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stated in
PubMed
issue
3
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stated in
PubMed
page(s)
305-23
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stated in
PubMed
exact match
https://scigraph.springernature.com/pub.10.1007/s00401-012-0996-2
0 references
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From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus
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Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
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Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease
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EphA1 interacts with integrin-linked kinase and regulates cell morphology and motility
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Assessment of Alzheimer's disease case-control associations using family-based methods
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SORL1 variants and risk of late-onset Alzheimer's disease
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GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers
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The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease
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The BAR domain proteins: molding membranes in fission, fusion, and phagy
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Interaction of the cytosolic domains of sorLA/LR11 with the amyloid precursor protein (APP) and beta-secretase beta-site APP-cleaving enzyme
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Neuronal sorting protein-related receptor sorLA/LR11 regulates processing of the amyloid precursor protein
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21 March 2017
Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease
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Amyloid plaque core protein in Alzheimer disease and Down syndrome
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21 March 2017
Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage
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21 March 2017
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
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Dense-core senile plaques in the Flemish variant of Alzheimer's disease are vasocentric
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APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy
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APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy
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A novel adaptor protein orchestrates receptor patterning and cytoskeletal polarity in T-cell contacts
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Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium
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21 March 2017
Candidate gene for the chromosome 1 familial Alzheimer's disease locus
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21 March 2017
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
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Ephrin signalling controls brain size by regulating apoptosis of neural progenitors
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21 March 2017
The carboxy terminus of the beta amyloid protein is critical for the seeding of amyloid formation: implications for the pathogenesis of Alzheimer's disease
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21 March 2017
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
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21 March 2017
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities
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21 March 2017
Genome-wide association study of Alzheimer's disease with psychotic symptoms
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Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
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Alzheimer's disease: Initial report of the purification and characterization of a novel cerebrovascular amyloid protein
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Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
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Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
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7 April 2017
Eph receptor signalling casts a wide net on cell behaviour
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7 April 2017
Secreted amyloid beta-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease
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7 April 2017
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7 April 2017
A genome-wide scan for common variants affecting the rate of age-related cognitive decline
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28 September 2017
Complement receptor 1 (CR1) and Alzheimer's disease
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28 September 2017
Association and expression analyses with single-nucleotide polymorphisms in TOMM40 in Alzheimer disease
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28 September 2017
TOMM40 poly-T repeat lengths, age of onset and psychosis risk in Alzheimer disease.
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Membrane shaping by the Bin/amphiphysin/Rvs (BAR) domain protein superfamily
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28 September 2017
APOE and Alzheimer disease: a major gene with semi-dominant inheritance
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28 September 2017
Amyloid precursor protein processing and Alzheimer's disease
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28 September 2017
CR1 is associated with amyloid plaque burden and age-related cognitive decline
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28 September 2017
Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE
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28 September 2017
Meta-analysis of the association between variants in SORL1 and Alzheimer disease
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28 September 2017
Evolution of CD33-related siglecs: regulating host immune functions and escaping pathogen exploitation?
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28 September 2017
Identification of novel loci for Alzheimer disease and replication of CLU, PICALM, and BIN1 in Caribbean Hispanic individuals
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28 September 2017
The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study
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28 September 2017
Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes
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28 September 2017
Cholesterol-related genes in Alzheimer's disease
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28 September 2017
Genome-wide analysis of genetic loci associated with Alzheimer disease
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28 September 2017
A presenilin-1 mutation identified in familial Alzheimer disease with cotton wool plaques causes a nearly complete loss of gamma-secretase activity
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28 September 2017
Genetic evidence for the involvement of lipid metabolism in Alzheimer's disease
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28 September 2017
Alzheimer's disease phenotypes and genotypes associated with mutations in presenilin 2.
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28 September 2017
gamma-secretases: from cell biology to therapeutic strategies
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28 September 2017
Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort
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28 September 2017
The pursuit of susceptibility genes for Alzheimer's disease: progress and prospects
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28 September 2017
A TOMM40 variable-length polymorphism predicts the age of late-onset Alzheimer's disease
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28 September 2017
Hidradenitis suppurativa
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28 September 2017
The role of apolipoprotein E in Alzheimer's disease
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28 September 2017
Clusterin: a forgotten player in Alzheimer's disease
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28 September 2017
Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis--a review
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28 September 2017
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28 September 2017
Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease
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Basic and clinical immunology of Siglecs
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28 September 2017
Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE.
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28 September 2017
BAR the door: cancer suppression by amphiphysin-like genes
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28 September 2017
A genome-wide association study for late-onset Alzheimer's disease using DNA pooling
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28 September 2017
Presenilins: members of the gamma-secretase quartets, but part-time soloists too.
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28 September 2017
No association of SORL1 SNPs with Alzheimer's disease.
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28 September 2017
Clinical and neuropathological features of the arctic APP gene mutation causing early-onset Alzheimer disease
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28 September 2017
Membrane traffic and muscle: lessons from human disease
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28 September 2017
Association between SORL1 and Alzheimer's disease in a genome-wide study
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28 September 2017
Enhanced accumulation of phosphorylated alpha-synuclein and elevated beta-amyloid 42/40 ratio caused by expression of the presenilin-1 deltaT440 mutant associated with familial Lewy body disease and variant Alzheimer's disease
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28 September 2017
Association between genetic variants in SORL1 and autopsy-confirmed Alzheimer disease
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28 September 2017
Role of ATP-binding cassette transporters in brain lipid transport and neurological disease
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28 September 2017
Cell-cell signaling via Eph receptors and ephrins
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28 September 2017
Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study
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28 September 2017
Endocytosis: clathrin-mediated membrane budding
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28 September 2017
A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch population
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28 September 2017
The association between genetic variants in SORL1 and Alzheimer disease in an urban, multiethnic, community-based cohort
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28 September 2017
The presenilin hypothesis of Alzheimer's disease: evidence for a loss-of-function pathogenic mechanism
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28 September 2017
Dementia and mortality in persons with Down's syndrome
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PubMed Central
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28 September 2017
Putative dual role of ephrin-Eph receptor interactions in inflammation
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28 September 2017
ABCA7 expression is regulated by cellular cholesterol through the SREBP2 pathway and associated with phagocytosis
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 September 2017
Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotype
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28 September 2017
Novel presenilin 1 mutation (S170F) causing Alzheimer disease with Lewy bodies in the third decade of life
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28 September 2017
Diverse roles of eph receptors and ephrins in the regulation of cell migration and tissue assembly
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PubMed Central
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28 September 2017
CD2AP localizes to the slit diaphragm and binds to nephrin via a novel C-terminal domain
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 September 2017
The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Abeta protofibril formation
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 September 2017
Identification of a CD20-, FcepsilonRIbeta-, and HTm4-related gene family: sixteen new MS4A family members expressed in human and mouse
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 September 2017
Amyloid angiopathy and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 September 2017
Eph receptors and ephrin ligands. essential mediators of vascular development.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 September 2017
Identification of a new multigene four-transmembrane family (MS4A) related to CD20, HTm4 and beta subunit of the high-affinity IgE receptor
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 September 2017
A pathogenic presenilin-1 deletion causes abberrant Abeta 42 production in the absence of congophilic amyloid plaques
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PubMed Central
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28 September 2017
Is epsilon4 the ancestral human apoE allele?
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 September 2017
Lewy bodies contain altered alpha-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genes
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 September 2017
Amyloid-beta-protein isoforms in brain of subjects with PS1-linked, beta APP-linked and sporadic Alzheimer disease
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 September 2017
Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): I--A review of clinical, radiologic and genetic aspects
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28 September 2017
Predominant deposition of amyloid-beta 42(43) in plaques in cases of Alzheimer's disease and hereditary cerebral hemorrhage associated with mutations in the amyloid precursor protein gene
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28 September 2017
Relative abundance of Alzheimer A beta amyloid peptide variants in Alzheimer disease and normal aging
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28 September 2017
APP717 missense mutation affects the ratio of amyloid beta protein species (A beta 1-42/43 and a beta 1-40) in familial Alzheimer's disease brain.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 September 2017
Type III hyperlipoproteinemia: a focus on lipoprotein receptor-apolipoprotein E2 interactions
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 September 2017
Neuropathological changes in scrapie and Alzheimer's disease are associated with increased expression of apolipoprotein E and cathepsin D in astrocytes
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 September 2017
Anti‐inflammatory agents as a therapeutic approach to Alzheimer's disease
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28 September 2017
Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 September 2017
Activation of EphA receptors on CD4+CD45RO+ memory cells stimulates migration
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31 May 2018
Clinical, neuropathologic, and biochemical profile of the amyloid precursor protein I716F mutation
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31 May 2018
Ephrin-B2 is differentially expressed in the intestinal epithelium in Crohn's disease and contributes to accelerated epithelial wound healing in vitro
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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31 May 2018
APOE and other loci affect age-at-onset in Alzheimer's disease families with PS2 mutation
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31 May 2018
Visualization of A beta 42(43) and A beta 40 in senile plaques with end-specific A beta monoclonals: evidence that an initially deposited species is A beta 42(43).
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31 May 2018
Occurrence of neuropathological changes and dementia of Alzheimer's disease in Down's syndrome.
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31 May 2018
Apolipoprotein E immunoreactivity in cerebral amyloid deposits and neurofibrillary tangles in Alzheimer's disease and kuru plaque amyloid in Creutzfeldt-Jakob disease.
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31 May 2018
TDP-43 pathological changes in early onset familial and sporadic Alzheimer's disease, late onset Alzheimer's disease and Down's syndrome: association with age, hippocampal sclerosis and clinical phenotype.
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28 November 2018
Expression profiling of the ephrin (EFN) and Eph receptor (EPH) family of genes in atherosclerosis-related human cells.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 November 2018
Mind the IGAP.
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28 November 2018
Endosomal clathrin drives actin accumulation at the immunological synapse.
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28 November 2018
Gamma-secretase gene mutations in familial acne inversa
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28 November 2018
Systematic Analysis of Candidate Genes for Alzheimer's Disease in a French, Genome-Wide Association Study
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28 November 2018
Identification of independent APP locus duplication in Japanese patients with early-onset Alzheimer disease.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 November 2018
SORL1 is genetically associated with Alzheimer disease in a Japanese population.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 November 2018
Novel extreme homozygote haplotypes at the human caveolin 1 gene upstream purine complex in sporadic Alzheimer's disease.
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28 November 2018
Association of SORL1 gene variants with Alzheimer's disease
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28 November 2018
Apolipoprotein E: structure determines function, from atherosclerosis to Alzheimer's disease to AIDS.
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28 November 2018
Generation and characterization of EphA1 receptor tyrosine kinase reporter knockout mice
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 November 2018
SORL1 is genetically associated with increased risk for late-onset Alzheimer disease in the Belgian population
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 November 2018
SORL1 haplotypes modulate risk of Alzheimer's disease in Chinese.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 November 2018
Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease.
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28 November 2018
A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 November 2018
Extreme cerebrospinal fluid amyloid beta levels identify family with late-onset Alzheimer's disease presenilin 1 mutation.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 November 2018
Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants
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28 November 2018
Molecular dissection of the interaction between amyloid precursor protein and its neuronal trafficking receptor SorLA/LR11.
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28 November 2018
Aberrant accentuation of neurofibrillary degeneration in the hippocampus of Alzheimer's disease with amyloid precursor protein 717 and presenilin-1 gene mutations.
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28 November 2018
A mutant PSEN1 causes dementia with Lewy bodies and variant Alzheimer's disease.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 November 2018
A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 November 2018
Apolipoprotein Eepsilon4 modifies Alzheimer's disease onset in an E280A PS1 kindred.
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28 November 2018
Two novel presenilin-1 mutations (Y256S and Q222H) are associated with early-onset Alzheimer's disease.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
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28 November 2018
Variability and heterogeneity in Alzheimer's disease with cotton wool plaques: a clinicopathological study of four autopsy cases.
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28 November 2018
Tau load is associated with apolipoprotein E genotype and the amount of amyloid beta protein, Abeta40, in sporadic and familial Alzheimer's disease.
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28 November 2018
Presenilin-1 mutation L271V results in altered exon 8 splicing and Alzheimer's disease with non-cored plaques and no neuritic dystrophy.
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28 November 2018
CD2-associated protein directly interacts with the actin cytoskeleton.
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28 November 2018
A novel mutation (G217D) in the Presenilin 1 gene ( PSEN1) in a Japanese family: presenile dementia and parkinsonism are associated with cotton wool plaques in the cortex and striatum
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28 November 2018
Dementia in hereditary cerebral hemorrhage with amyloidosis-Dutch type is associated with cerebral amyloid angiopathy but is independent of plaques and neurofibrillary tangles.
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28 November 2018
Dementia in people with Down's syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
Cotton wool plaques in non-familial late-onset Alzheimer disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
A novel presenilin mutation (M233V) causing very early onset Alzheimer's disease with Lewy bodies.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
LR11, a mosaic LDL receptor family member, mediates the uptake of ApoE-rich lipoproteins in vitro
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
Novel amyloid precursor protein mutation in an Iowa family with dementia and severe cerebral amyloid angiopathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
Variant Alzheimer disease with spastic paraparesis: neuropathological phenotype
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
Distinguishable effects of presenilin-1 and APP717 mutations on amyloid plaque deposition.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
The impact of different presenilin 1 andpresenilin 2 mutations on amyloid deposition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain: evidence for other phenotype-modifying factors.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
Presenile Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692Ala-->Gly mutation.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
Early amyloid deposition in the medial temporal lobe of young Down syndrome patients: a regional quantitative analysis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
Pathology of familial Alzheimer's disease with Lewy bodies.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
Further evidence for an association between a mutation in the APP gene and Lewy body formation.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
Amyloid (Abeta) deposition in chromosome 1-linked Alzheimer's disease: the Volga German families.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
Amyloid beta protein (Abeta) deposition in chromosome 14-linked Alzheimer's disease: predominance of Abeta42(43).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
Familial and sporadic Alzheimer's disease: neuropathology cannot exclude a final common pathway.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
Alzheimer's disease and possible gene interaction.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
Lewy bodies in the brain of two members of a family with the 717 (Val to Ile) mutation of the amyloid precursor protein gene.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3708460
retrieved
28 November 2018
Amyloid beta protein 1-42/43 (A beta 1-42/43) in cerebellar diffuse plaques: enzyme-linked immunosorbent assay and immunocytochemical study
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22618995
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The Biology of Genomes. Disease risk links to gene regulation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22618995
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The classification of cyclooxygenase inhibitors
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22618995
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22618995
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Positional effects of presenilin-1 mutations on tau phosphorylation in cortical plaques
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22618995
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1007/S00401-012-0996-2
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1741631
Dimensions Publication ID
1017401436
0 references
OpenCitations bibliographic resource ID
1741631
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1741631
PMCID
3708460
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1741631
PubMed ID
22618995
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1741631
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