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Showing results 1 to 12 of 12

	Title	Author(s)	Issue Date
	Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOE Journal:Neuroscience Letters	Song, YQ Rogaeva, E Premkumar, S Brindle, N Kawarai, T Orlacchio, A Yu, G Levesque, G Nishimura, M Ikeda, M Pei, Y O'Toole, C Duara, R Barker, W Sorbi, S Freedman, M Farrer, L St GeorgeHyslop, P	1998
	Alleles at the Nicastrin locus modify presenilin 1-deficiency phenotype Journal:Proceedings of the National Academy of Sciences of the United States of America	Rozmahel, R Mount, HTJ Chen, F Nguyen, V Huang, J Erdebil, S Liauw, J Yu, G Hasegawa, H Gu, Y Song, YQ Schmidt, SD Nixon, RA Mathews, PM Bergeron, C Fraser, P Westaway, D St GeorgeHyslop, P	2002
	Analysis of the butyrylcholinesterase gene and nearby chromosome 3 markers in Alzheimer disease Journal:Human Molecular Genetics	Brindle, N Song, Y Rogaeva, E Premkumar, S Levesque, G Yu, G Ikeda, M Nishimura, M Paterson, A Sorbi, S Duara, R Farrer, L St GeorgeHyslop, P	1998
	Carboxyl-terminal fragments of alzheimer β-amlyloid precursor protein accumulate in restricted and unpredicted intracellular compartments in presenilin 1-deficient cells Journal:Journal of Biological Chemistry	Chen, F Yang, DS Petanceska, S Yang, A Tandon, A Yu, G Rozmahel, R Ghiso, J Nishimura, M Zhang, DM Kawarai, T Levesque, G Mills, J Levesque, L Song, YQ Rogaeva, E Westaway, D Mount, H Gandy, S St GeorgeHyslop, P Fraser, PE	2000
	A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic families Journal:Journal of the American Medical Association	Athan, ES Williamson, J Ciappa, A Santana, V Romas, SN Lee, JH Rondon, H Lantigua, RA Medrano, M Torres, M Arawaka, S Rogaeva, E Song, YQ Sato, C Kawarai, T Fafel, KC Boss, MA Seltzer, WK Stern, Y St GeorgeHyslop, P Tycko, B Mayeux, R	2001
	Mutation of conserved aspartates affect maturation of presenilin 1 and presenilin 2 complexes Journal:Acta Neurologica Scandinavica, Supplement	Yu, G Chen, F Nishimura, M Steiner, H Tandon, A Kawarai, T Arawaka, S Supala, A Song, YQ Rogaeva, E Holmes, E Zhang, DM Milman, P Fraser, P Haass, C St GeorgeHyslop, P	2000
	Mutation of conserved aspartates affects maturation of both aspartate mutant and endogenous presenilin 1 and presenilin 2 complexes Journal:Journal of Biological Chemistry	Yu, G Chen, F Nishimura, M Steiner, H Tandon, A Kawarai, T Arawaka, S Supala, A Song, YQ Rogaeva, E Holmes, E Zhang, DM Milman, P Fraser, PE Haass, C St GeorgeHyslop, P	2000
	Mutation of the conserved N-terminal cysteine (Cys92) of human presenilin 1 causes increased Aβ42 secretion in mammalian cells but impaired Notch/lin-12 signalling in C. elegans Journal:NeuroReport	Dong Mei Zhang Levitan, D Yu, G Nishimura, M Chen, F Tandon, A Kawarai, T Arawaka, S Supala, A Song, YQ Rogaeva, E Liang, Y Holmes, E Milman, P Sato, C Zhang, L St GeorgeHyslop, P	2000
	Mutations in the open reading frame of the β-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease Journal:Neurogenetics	Nicolaou, M Song, YQ Sato, CA Orlacchio, A Kawarai, T Medeiros, H Liang, Y Sorbi, S Richard, E Rogaev, EI Moliaka, Y Bruni, AC Jorge, R Percy, M Duara, R Farrer, LA St GeorgeHyslop, P Rogaeva, EA	2001
	The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease Journal:Nature Genetics	Rogaeva, E Meng, Y Lee, JH Gu, Y Kawarai, T Zou, F Katayama, T Baldwin, CT Cheng, R Hasegawa, H Chen, F Shibata, N Lunetta, KL PardossiPiquard, R Bohm, C Wakutani, Y Cupples, LA Cuenco, KT Green, RC Pinessi, L Rainero, I Sorbi, S Bruni, A Duara, R Friedland, RP Inzelberg, R Hampe, W Bujo, H Song, YQ Andersen, OM Willnow, TE GraffRadford, N Petersen, RC Dickson, D Der, SD Fraser, PE SchmittUlms, G Younkin, S Mayeux, R Farrer, LA St GeorgeHyslop, P	2007
	Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer disease Journal:Archives of Neurology	Devi, G Fotiou, A Jyrinji, D Tycko, B DeArmand, S Rogaeva, E Song, YQ Medieros, H Liang, Y Orlacchio, A Williamson, J St GeorgeHyslop, P Mayeux, R	2000
	Screening for PS1 mutations in a referral-based series of AD cases: 21 Novel mutations Journal:Neurology	Rogaeva, EA Fafel, KC Song, YQ Medeiros, H Sato, C Liang, Y Richard, E Rogaev, EI Frommelt, P Sadovnick, AD Meschino, W Rockwood, K Boss, MA Mayeux, R St GeorgeHyslop, P	2001

Showing results 1 to 12 of 12