Patterns and severity of vascular amyloid in Alzheimer's disease associated with duplications and missense mutations in APP gene, Down syndrome and sporadic Alzheimer's disease (Q60721200)

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English	Patterns and severity of vascular amyloid in Alzheimer's disease associated with duplications and missense mutations in APP gene, Down syndrome and sporadic Alzheimer's disease	article

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26 March 2020

Patterns and severity of vascular amyloid in Alzheimer's disease associated with duplications and missense mutations in APP gene, Down syndrome and sporadic Alzheimer's disease (English)

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26 March 2020

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Alzheimer's disease

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1

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26 March 2020

Andrew Robinson

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26 March 2020

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26 March 2020

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26 March 2020

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Yvonne S Davidson

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26 March 2020

Nancy Allen

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26 March 2020

Tadafumi Hashimoto

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26 March 2020

Anna Richardson

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26 March 2020

Matthew Jones

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26 March 2020

Julie S Snowden

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26 March 2020

Marie-Claude Potier

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26 March 2020

Annie Laquerrière

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26 March 2020

Vee Prasher

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26 March 2020

Takeshi Iwatsubo

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26 March 2020

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16 May 2018

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26 March 2020

Acta Neuropathologica

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26 March 2020

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26 March 2020

4

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26 March 2020

569-587

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26 March 2020

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Creative Commons Attribution 4.0 International

16 May 2018

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April 2022 Public Data File from Crossref

copyright status

0 references

Apolipoprotein E genotyping by one-stage PCR

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuropathological stageing of Alzheimer-related changes

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part II. Standardization of the neuropathologic assessment of Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The site of the earliest lesions of Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amyloid beta protein (A beta) deposition: A beta 42(43) precedes A beta 40 in Down syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amyloid-associated proteins α1-antichymotrypsin and apolipoprotein E promote assembly of Alzheimer β-protein into filaments

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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).

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High tissue content of soluble beta 1-40 is linked to cerebral amyloid angiopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abeta-peptide length and apolipoprotein E genotype in Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The apolipoprotein E epsilon 4 allele is associated with increased neuritic plaques and cerebral amyloid angiopathy in Alzheimer's disease and Lewy body variant

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preferential deposition of amyloid beta protein (Abeta) in the form Abeta40 in Alzheimer's disease is associated with a gene dosage effect of the apolipoprotein E E4 allele.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular mapping of Alzheimer-type dementia in Down's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amyloid angiopathy and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cases of Alzheimer's disease due to deletion of exon 9 of the presenilin-1 gene show an unusual but characteristic beta-amyloid pathology known as 'cotton wool' plaques.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phases of A beta-deposition in the human brain and its relevance for the development of AD.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alzheimer disease and Down syndrome: factors in pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Qualitative neuropsychological performance characteristics in frontotemporal dementia and Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotype associated with APP duplication in five families

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low prevalence of APP duplications in Swedish and Finnish patients with early-onset Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intrafamilial diversity of phenotype associated with app duplication.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microvasculature changes and cerebral amyloid angiopathy in Alzheimer's disease and their potential impact on therapy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of independent APP locus duplication in Japanese patients with early-onset Alzheimer disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Capillary cerebral amyloid angiopathy identifies a distinct APOE epsilon4-associated subtype of sporadic Alzheimer's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK series

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No evidence of APP point mutation and locus duplication in individuals with cerebral amyloid angiopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human apoE isoforms differentially regulate brain amyloid-β peptide clearance

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical diagnosis of early-onset dementias: diagnostic accuracy and clinicopathological relationships.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation screening of patients with Alzheimer disease identifies APP locus duplication in a Swedish patient

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

National Institute on Aging-Alzheimer's Association guidelines for the neuropathologic assessment of Alzheimer's disease: a practical approach

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

National Institute on Aging-Alzheimer's Association guidelines for the neuropathologic assessment of Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy for synaptojanin1 in Down syndrome is functionally linked to the enlargement of early endosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patterns of cerebral amyloid angiopathy define histopathological phenotypes in Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Large APP locus duplication in a sporadic case of cerebral haemorrhage

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brain distribution of dipeptide repeat proteins in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in the 3'untranslated region of APP as a genetic determinant of cerebral amyloid angiopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence that the rab5 effector APPL1 mediates APP-βCTF-induced dysfunction of endosomes in Down syndrome and Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Morbidity and medication in a large population of individuals with Down syndrome compared to the general population

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk of Major Cardiovascular Events in People with Down Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impact of sex and APOE4 on cerebral amyloid angiopathy in Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Down Syndrome, Partial Trisomy 21, and Absence of Alzheimer's Disease: The Role of APP.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical aspects and biomarkers of Alzheimer's disease in Down syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dysfunction of autophagy and endosomal-lysosomal pathways: Roles in pathogenesis of Down syndrome and Alzheimer's Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebrovascular pathology in Down syndrome and Alzheimer disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/29770843

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00401-018-1866-3

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29770843 AND SRC:MED&resulttype=core&format=json

26 March 2020

PMC publication ID

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29770843 AND SRC:MED&resulttype=core&format=json

26 March 2020

PubMed publication ID

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29770843 AND SRC:MED&resulttype=core&format=json

26 March 2020

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