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Proceedings of the National Academy of Sciences of the United States of America|November 8, 1994
Isoform-specific interactions of apolipoprotein E with microtubule-associated protein tau: implications for Alzheimer diseaseW J Strittmatter, A M Saunders, M Goedert, et al.Prenatal Diagnosis|July 1, 1988
Prenatal diagnosis using deletion studies in Duchenne muscular dystrophyM C Speer, M A Pericak-Vance, L H Yamaoka, et al.Neurology|September 1, 1987
Hereditary motor and sensory neuropathy, X-linked: a half century follow-upM P Rozear, M A Pericak-Vance, K Fischbeck, et al.Nature|September 10, 1987
The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid beta-protein geneR E Tanzi, P H St George-Hyslop, J L Haines, et al.Neurobiology of Aging|September 1, 1989
Familial Alzheimer's disease: progress and problemsP H St George-Hyslop, R H Myers, J L Haines, et al.The Pharmacogenomics Journal|February 1, 2006
Efficacy of rosiglitazone in a genetically defined population with mild-to-moderate Alzheimer's diseaseM E Risner, A M Saunders, J F B Altman, et al.Nature|August 4, 1985
Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segmentA P Monaco, C J Bertelson, W Middlesworth, et al.Neuroscience Letters|November 21, 1994
Isoform-specific interactions of apolipoprotein E with the microtubule-associated protein MAP2c: implications for Alzheimer's diseaseD Y Huang, M Goedert, R Jakes, et al.American Journal of Human Genetics|September 1, 1991
APP717, APP693, and PRIP gene mutations are rare in Alzheimer diseaseG D Schellenberg, L Anderson, S O'dahl, et al.Science (New York, N.Y.)|August 13, 1993
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset familiesE H Corder, A M Saunders, W J Strittmatter, et al.Pageof 37