(Q43597292)

25 November 2017

title

Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14. (English)

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25 November 2017

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25

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25 November 2017

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Rogaeva E

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25 November 2017

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Haines J

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Peter Henry St George-Hyslop

25 November 2017

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object named as

St George-Hyslop P

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25 November 2017

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Gusella J

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Margaret A. Pericak-Vance

25 November 2017

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Pericak-Vance M

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25 November 2017

Rogaev E

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25 November 2017

Mortilla M

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25 November 2017

Vaula G

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25 November 2017

Foncin JF

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25 November 2017

Montesi M

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25 November 2017

Bruni A

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25 November 2017

Sorbi S

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25 November 2017

Rainero I

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25 November 2017

Pinessi L

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25 November 2017

Pollen D

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25 November 2017

Polinsky R

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25 November 2017

Nee L

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25 November 2017

Kennedy J

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25 November 2017

Macciardi F

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25 November 2017

Liang Y

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25 November 2017

Alexandrova N

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25 November 2017

Lukiw W

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25 November 2017

Schlumpf K

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25 November 2017

Tanzi R

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25 November 2017

Tsuda T

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25 November 2017

Cantu JM

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25 November 2017

Duara R

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25 November 2017

Amaducci L

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25 November 2017

Bergamini L

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25 November 2017

Roses A

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25 November 2017

Crapper McLachlan D

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25 November 2017

language of work or name

English

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publication date

1 December 1992

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25 November 2017

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25 November 2017

volume

2

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25 November 2017

issue

4

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25 November 2017

page(s)

330-334

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Familial Alzheimer's disease: progress and problems

25 November 2017

cites work

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https://api.crossref.org/works/10.1038%2FNG1292-330

Predisposing locus for Alzheimer's disease on chromosome 21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the beta-amyloid precursor protein gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

Genetic linkage studies in Alzheimer's disease families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

Mechanisms of amyloid deposition in Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

Linkage of an Alzheimer disease susceptibility locus to markers on human chromosome 21

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

7 January 2021

The genetic defect causing familial Alzheimer's disease maps on chromosome 21.

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

7 January 2021

A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

7 January 2021

Regulation and genetic control of brain amyloid. FESN Study Group

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

7 January 2021

Report of the committee on the genetic constitution of chromosome 14.

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

7 January 2021

Alzheimer's disease: Genetic aspects and associated clinical disorders

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

7 January 2021

Continuous linkage map of human chromosome 14 short tandem repeat polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

7 January 2021

Absence of Linkage of Chromosome 21q21 Markers to Familial Alzheimer's Disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

7 January 2021

More missense in amyloid gene.

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

7 January 2021

A physical map of the human PI and AACT genes

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

7 January 2021

Physical mapping of probes within 14q32, a subtelomeric region showing a high recombination frequency

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

7 January 2021

Characterization of the 5'-end region and the first two exons of the beta-protein precursor gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

7 January 2021

The expression of the amyloid precursor protein (APP) is regulated by two GC-elements in the promoter

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-330

7 January 2021

Identifiers

DOI

10.1038/NG1292-330

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Dimensions Publication ID

25 November 2017

1001816437

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