(Q44456153)

3 December 2017

title

Absence of association between Alzheimer disease and the regulatory region polymorphism of the PS2 gene in an Italian population (English)

1 reference

3 December 2017

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12

Ekaterina Rogaeva

1 reference

3 December 2017

3

Toshitaka Kawarai

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3 December 2017

7

Benedetta Nacmias

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3 December 2017

9

Sandro Sorbi

1 reference

Peter Henry St George-Hyslop

3 December 2017

object named as

Peter H St George-Hyslop

10

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Amalia Bruni

11

object named as

Amalia C Bruni

1 reference

3 December 2017

6

Christine Sato

1 reference

3 December 2017

8

Nobuto Shibata

1 reference

3 December 2017

5

Carmine Tomaino

1 reference

3 December 2017

1

Manuela Di Natale

1 reference

3 December 2017

Maria Caterina Di Perri

2

object named as

Maria Perri

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3 December 2017

4

Raffaele Maletta

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3 December 2017

author name string

Peter H St George-Hyslop

10

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3 December 2017

language of work or name

English

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publication date

1 June 2003

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3 December 2017

June 2003

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published in

Neuroscience Letters

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3 December 2017

volume

343

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3 December 2017

issue

3

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3 December 2017

page(s)

210-212

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Identification of multiple loci for Alzheimer disease in a consanguineous Israeli-Arab community.

3 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900335-5

7 January 2021

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900335-5

7 January 2021

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900335-5

7 January 2021

Regulatory region variability in the human presenilin-2 (PSEN2) gene: potential contribution to the gene activity and risk for AD.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900335-5

7 January 2021

Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900335-5

7 January 2021

The solved and unsolved mysteries of the genetics of early-onset Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900335-5

7 January 2021

Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900335-5

7 January 2021

Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900335-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900335-5

7 January 2021

Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900335-5

7 January 2021

Transcriptional regulation of Alzheimer's disease genes: implications for susceptibility

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900335-5

7 January 2021

10.1016/S0304-3940(03)00335-5

Identifiers

DOI

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1 reference