Etiological Clues from Gene Defects Causing Early Onset Familial Alzheimer’s Disease
- 1 January 1997
- book chapter
- Published by Springer Nature
Abstract
No abstract availableKeywords
This publication has 84 references indexed in Scilit:
- Molecular Analysis of the Presenilin 1 (S182) Gene in “Sporadic” Cases of Alzheimer's Disease: Identification and Characterisation of Unusual Splice VariantsJournal of Neurochemistry, 2002
- Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's diseaseThe Lancet, 1996
- Presenilins and Alzheimer diseaseNature Genetics, 1995
- Facilitation of lin-12-mediated signalling by sel-12, a Caenorhabditis elegans S182 Alzheimer's disease geneNature, 1995
- Missense mutation of S182 gene in Japanese familial Alzheimer's diseaseThe Lancet, 1995
- APP processing, Aβ-amyloidogenesis, and the pathogenesis of Alzheimer's diseaseNeurobiology of Aging, 1994
- Isolation and characterization of APLP2 encoding a homologue of the Alzheimer's associated amyloid β protein precursorNature Genetics, 1993
- Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's diseaseNature, 1991
- Detection of soluble forms of the β-amyloid precursor protein in human plasmaBiochemical and Biophysical Research Communications, 1990
- Alzheimer's disease: Initial report of the purification and characterization of a novel cerebrovascular amyloid proteinBiochemical and Biophysical Research Communications, 1984