Evidence against association of the FE65 gene (APBB1) intron 13 polymorphism in Alzheimer's patients (Q73251852)

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2 November 2019

title

Evidence against association of the FE65 gene (APBB1) intron 13 polymorphism in Alzheimer's patients (English)

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2 November 2019

3

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2 November 2019

Benjamin Bakondi

4

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2 November 2019

author name string

S Y Guénette

1

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2 November 2019

L Bertram

2

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2 November 2019

B T Hyman

5

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2 November 2019

G W Rebeck

6

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2 November 2019

R E Tanzi

7

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2 November 2019

D Blacker

8

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2 November 2019

language of work or name

English

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publication date

1 December 2000

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2 November 2019

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2 November 2019

volume

296

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2 November 2019

issue

1

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2 November 2019

page(s)

17-20

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No evidence for genetic association or linkage of the cathepsin D (CTSD) exon 2 polymorphism and Alzheimer disease.

2 November 2019

cites work

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Alpha-2 macroglobulin is genetically associated with Alzheimer disease.

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7 January 2021

Mapping of the human and murine X11-like genes (APBA2 and apba2), the murine Fe65 gene (Apbb1), and the human Fe65-like gene (APBB2): genes encoding phosphotyrosine-binding domain proteins that interact with the Alzheimer's disease amyloid [...]

1 reference

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7 January 2021

The phosphotyrosine interaction domains of X11 and FE65 bind to distinct sites on the YENPTY motif of amyloid precursor protein

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7 January 2021

Clinical and pathological correlates of apolipoprotein E ?4 in Alzheimer's disease

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Significant evidence for linkage disequilibrium over a 5-cM region among Afrikaners

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7 January 2021

Association of a novel human FE65-like protein with the cytoplasmic domain of the beta-amyloid precursor protein

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7 January 2021

A discordant-sibship test for disequilibrium and linkage: no need for parental data

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7 January 2021

The human FE65 gene: genomic structure and an intronic biallelic polymorphism associated with sporadic dementia of the Alzheimer type

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7 January 2021

A full genome scan for late onset Alzheimer's disease.

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Analysis of association at single nucleotide polymorphisms in the APOE region.

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Genetic polymorphism of cathepsin D is strongly associated with the risk for developing sporadic Alzheimer's disease.

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7 January 2021

Enhanced release of amyloid beta-protein from codon 670/671 "Swedish" mutant beta-amyloid precursor protein occurs in both secretory and endocytic pathways

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7 January 2021

Regulation of beta-amyloid secretion by FE65, an amyloid protein precursor-binding protein

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7 January 2021

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 January 2021

A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test

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7 January 2021

Molecular cloning of human Fe65L2 and its interaction with the Alzheimer's beta-amyloid precursor protein

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7 January 2021

10.1016/S0304-3940(00)01607-4

Identifiers

DOI

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2 November 2019

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