References
- Hardy J, Duff K. Heterogeneity in Alzeimer’s Disease. Ann Med 1993; 25: 437-40.
- Suzuki N, Cheung TT, Xai XD, et al. An increased percentage of long amyloid beta-protein secreted by familial amyloid beta-protein precursor (APP717) mutants. Science 1994; 264: 1336-40.
- Haass C, Hung AY, Selkoe DJ, Teplow DB. Mutations associated with a locus for familial Alzheimer’s disease result in alternative processing of amyloid P-protein precursor. J Biol Chem. 1994; 269: 17741 -8.
- Corder EH, Saunders AM, Strittmatter WJ, et al. Gene dose of Apolipoprotein E type 4 allele and the risk of Alzheimer’s disease in late onset families. Science 1993; Sherrington R, Roagaev El, Liang Y, et al. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer’s disease. Nature 1995; 375: 754-60.
- Levy-Lahad E, Wasco W, Wijsman E, et al. Candidate locus for the chromosome 1 familial Alzheimer’s disease locus. Science 1995; 268: 973-7.
- Poirier J, Hess M, May P, Finch CE. Astrocytic apolipoprotein E mRNA and GFAP mRNA in hippocampus after entorhinal cortex lesions. Mol Brain Res 1991; 11: 97-106.
- Namba Y, Tomonaga M, Kawasaki H, Otono E, lkeda K. Apolipoprotein E immunoreactivity in cerebral deposits and neurofibrillary tangles in Alzheimer’s disease and kuru plaque amyloid in Creuzfeldt-Jakob disease. Brain Res 1991; 541: 163-6.
- Wisniewski T, Frangione B. Apolipoprotein E: a pathological chaperone protein in patients with cerebral and systemic amyloid. Neurosci Left 1993; 135: 235-9.
- Schellenberg GD, Deeb SS, Boehnke M, et al. Association of an apolipoprotein CII allele with familial dementia of the Alzheimer type. J Neurogenet 1987; 4: 97-108.
- Strittmatter WJ, Saunders AM, Schmechel D, et al. Apolipoprotein E: high avidity binding to beta-amyloid and increased frequency of type 4 allele in late onset familial Alzheimer’s disease. Proc Natl Acad Sci USA 1993; 90:
- Kuusisto J, Koivisto K, Kervinen K, et al. Association of apolipoprotein E phenotypes with last onset Alzheimer’s disease: population based study. BMJ 1994; 309: 636-8.
- Levitan D, Greenwald 1. Facilitation of lin-12 mediated signaling by sel-12, a Caenorhabditis elegans S182 Alzheimer’s disease gene. Nature 1995; 377: 351 -4.
- Hernault SW, Arduengo PM. Mutation of a putative sperm membrane protein in Caenorhabditis elegans prevents sperm differentiation but not its associated meiotic divisions. J Cell Biol 1992; 1 19: 55-68.
- Wang Q, Curran ME, Spawski I, et al. Positional cloning of a novel potassium channel gene: KVLQTl mutations cause cardiac arrhythmias. Nat Genet 1995; 12: 17-23.
- Querfurth PH, Wijsman EM, St. George Hyslop P, et al. p APP mRNA is increased in cultured fibroblasts from the familial Alzheimer’s disease-1 family. Mol Brain Res 1995: 28; 319-37.