(Q36854788)

English

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

scientific article published on 28 December 2010

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scholarly article

1 reference

Europe PubMed Central

16 August 2017

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 (English)

1 reference

Europe PubMed Central

16 August 2017

prion protein family

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1 reference

based on heuristic

inferred from title

object named as

James Lowe

10

0 references

object named as

Martin Rossor

11

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3

object named as

Rita Guerreiro

1 reference

Europe PubMed Central

16 August 2017

John Anthony Hardy

8

object named as

John Hardy

1 reference

Europe PubMed Central

16 August 2017

12

object named as

John Collinge

1 reference

Europe PubMed Central

16 August 2017

author name string

Daniel McNaughton

1

1 reference

Europe PubMed Central

16 August 2017

William Knight

2

1 reference

Europe PubMed Central

16 August 2017

Natalie Ryan

4

1 reference

Europe PubMed Central

16 August 2017

Jessica Lowe

5

1 reference

Europe PubMed Central

16 August 2017

Mark Poulter

6

1 reference

Europe PubMed Central

16 August 2017

David J Nicholl

7

1 reference

Europe PubMed Central

16 August 2017

Tamas Revesz

9

1 reference

Europe PubMed Central

16 August 2017

Simon Mead

13

1 reference

Europe PubMed Central

16 August 2017

publication date

28 December 2010

1 reference

Europe PubMed Central

16 August 2017

Neurobiology of Aging

1 reference

Europe PubMed Central

16 August 2017

33

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Europe PubMed Central

16 August 2017

2

1 reference

Europe PubMed Central

16 August 2017

426.e13-21

1 reference

Europe PubMed Central

16 August 2017

A phase 2 multiple ascending dose trial of bapineuzumab in mild to moderate Alzheimer disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

29 September 2017

Preventing prion pathogenicity by targeting the cellular prion protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

29 September 2017

Copy-number variation and association studies of human disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

29 September 2017

The genetics of neurodegenerative diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

29 September 2017

Down syndrome, Alzheimer's disease and seizures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

29 September 2017

Prion diseases of humans and animals: their causes and molecular basis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

29 September 2017

Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

29 September 2017

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

29 September 2017

Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

27 June 2018

No evidence for prion protein gene locus multiplication in Creutzfeldt-Jakob disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

4 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

4 September 2018

Intrafamilial diversity of phenotype associated with app duplication.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

4 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

4 September 2018

Phenotype associated with APP duplication in five families.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

4 September 2018

CSF biomarkers for Alzheimer's Disease: levels of beta-amyloid, tau, phosphorylated tau relate to clinical symptoms and survival

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

4 September 2018

Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

4 September 2018

Hereditary dementia with intracerebral hemorrhages and cerebral amyloid angiopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3657692

4 September 2018

Identifiers

10.1016/J.NEUROBIOLAGING.2010.10.010

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

16 August 2017

ResearchGate publication ID

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