Identification of a novel mutation in the presenilin 1 gene in a Chinese Alzheimer's disease family (Q46802866)

http://europepmc.org/abstract/MED/24737487

25 December 2017

title

Identification of a novel mutation in the presenilin 1 gene in a Chinese Alzheimer's disease family (English)

1 reference

http://europepmc.org/abstract/MED/24737487

25 December 2017

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9

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14 June 2020

author name string

Bo Deng

1

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14 June 2020

Yan Lian

2

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14 June 2020

Xin Wang

3

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14 June 2020

Fan Zeng

4

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14 June 2020

Bin Jiao

5

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14 June 2020

Ye-Ran Wang

6

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14 June 2020

Chun-Rong Liang

7

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14 June 2020

Yu-Hui Liu

8

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14 June 2020

Xiu-Qing Yao

10

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14 June 2020

Chi Zhu

11

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14 June 2020

Lu Shen

12

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14 June 2020

Hua-Dong Zhou

13

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14 June 2020

Tao Zhang

14

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14 June 2020

Yan-Jiang Wang

15

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14 June 2020

publication date

16 April 2014

1 reference

http://europepmc.org/abstract/MED/24737487

25 December 2017

published in

Neurotoxicity Research

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14 June 2020

volume

26

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14 June 2020

page(s)

211-215

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14 June 2020

issue

3

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https://scigraph.springernature.com/pub.10.1007/s12640-014-9462-3

14 June 2020

exact match

0 references

cites work

Locus-specific mutation databases for neurodegenerative brain diseases

1 reference

https://api.crossref.org/works/10.1007%2FS12640-014-9462-3

Deficiency of presenilin-1 inhibits the normal cleavage of amyloid precursor protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12640-014-9462-3

High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12640-014-9462-3

A novel presenilin 1 mutation (Ser169del) in a Chinese family with early-onset Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12640-014-9462-3

Vascular risk factors promote conversion from mild cognitive impairment to Alzheimer disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12640-014-9462-3

Mild cognitive impairment: clinical characterization and outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12640-014-9462-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12640-014-9462-3

The relationship between single nucleotide polymorphisms of the NTRK2 gene and sporadic Alzheimer's disease in the Chinese Han population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12640-014-9462-3

One novel presenilin-1 gene mutation in a Chinese pedigree of familial Alzheimer's disease

21 January 2018

1 reference

12 December 2020

Presenilin-1 mutations in Alzheimer's disease: an update on genotype-phenotype relationships

1 reference

12 December 2020

[Mutation site of presenilin-1 gene in familial Alzheimer's disease]

1 reference

12 December 2020

Clinical-genetic correlations in familial Alzheimer's disease caused by presenilin 1 mutations.

1 reference

12 December 2020

Presenilin structure in mechanisms leading to Alzheimer's disease

1 reference

12 December 2020

A novel APP mutation (D678H) in a Taiwanese patient exhibiting dementia and cerebral microvasculopathy

1 reference

12 December 2020

10.1007/S12640-014-9462-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24737487%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

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