(Q46925196)

English

Familial cases presenting very early onset autosomal dominant Alzheimer's disease with I143T in presenilin-1 gene: implication for genotype-phenotype correlation

scientific article published on 30 October 2007

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scholarly article

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Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

Familial cases presenting very early onset autosomal dominant Alzheimer's disease with I143T in presenilin-1 gene: implication for genotype-phenotype correlation (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

Alzheimer's disease

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author name string

Noritoshi Arai

1

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

Atsushi Kishino

2

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

Yuji Takahashi

3

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

Daiji Morita

4

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

Koichiro Nakamura

5

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

Takahiro Yokoyama

6

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

Tomoji Watanabe

7

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

Masayoshi Ida

8

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

Jun Goto

9

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

Shoji Tsuji

10

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

publication date

30 October 2007

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

9

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

1

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

65-67

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

Early-onset Alzheimer's disease in 2 large Belgian families

1 reference

https://api.crossref.org/works/10.1007%2FS10048-007-0104-2

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10048-007-0104-2

21 January 2018

Enhancement of amyloid beta 42 secretion by 28 different presenilin 1 mutations of familial Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17968601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathogenic presenilin 1 mutations (P436S & I143F) in early-onset Alzheimer's disease in the UK. Mutations in brief no. 223. Online.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17968601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17968601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Systematic genetic study of Alzheimer disease in Latin America: mutation frequencies of the amyloid beta precursor protein and presenilin genes in Colombia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17968601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New developments in high-throughput resequencing and variation detection using high density microarrays

1 reference

https://pubmed.ncbi.nlm.nih.gov/17968601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel presenilin 1 mutation with profound neurofibrillary pathology in an indigenous Southern African family with early-onset Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17968601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10048-007-0104-2

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

release_k6lsstkw6nfermdnysahzhbrji

1 reference

https://api.fatcat.wiki/v0/release/k6lsstkw6nfermdnysahzhbrji

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17968601

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