A unique gene expression signature discriminates familial Alzheimer's disease mutation carriers from their wild-type siblings-Reference-Cited by-同舟云学术

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A unique gene expression signature discriminates familial Alzheimer's disease mutation carriers from their wild-type siblings

Published:2005-09-30 Issue:41 Volume:102 Page:14854-14859
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Nagasaka Y.,Dillner K.,Ebise H.,Teramoto R.,Nakagawa H.,Lilius L.,Axelman K.,Forsell C.,Ito A.,Winblad B.,Kimura T.,Graff C.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference36 articles.

1. 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

2. Deciphering the Genetic Basis of Alzheimer's Disease

3. A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N–terminus of β–amyloid

4. The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families

5. The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Aβ protofibril formation

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