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Showing results 6 to 19 of 19 < previous

	Title	Author(s)	Issue Date	Views
	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	119
	Further analysis of the nicastrin: presenilin complex” Book:Notch from Neurodevelopment to Neurodegeneration: Keeping the Fate	Chen, F Yu, G Arawaka, S Nishimura, M Kawarai, T Yu, H Tandon, A Supala, A Song, Y Rogaeva, E Milman, P Sato, C Lee, J Song, L Zhang, L Fraser, PE St George-Hyslop, P	2006	144
	Low frequency of TAU mutations and further genetic heterogeneity in FTD Proceeding/Conference:International Conference on Alzheimer's Disease & Related Disorders	Kawarai, T Rogaeva, E Song, YQ Moliaka, Y Medeiros, H Liang, Y Sato, C Ling, S Fong, M Kolesnikova, T Bergeron, C Lang, AE Paterson, AD Orlacchio, A Bernardi, G Rockwood, K Allegri, R Rainero, I Pinessi, L Cappa, G Kertesz, A Bruni, AC Freedman, M Ahern, GL Tuite, P Fornazzari, L St George-Hyslop, P	2002	117
	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	134
	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	110
	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	134
	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	145
	Nicastrin binds to membrane-tethered Notch Journal:Nature Cell Biology	Chen, F Yu, G Arawaka, S Nishimura, M Kawarai, T Yu, H Tandon, A Supala, A Song, YQ Rogaeva, E Milman, P Sato, C Yu, C Janus, C Lee, J Song, L Zhang, L Fraser, PE St GeorgeHyslop, PH	2001	146
	Nicastrin modulates presenilin-mediated notch/glp-1 signal transduction and βAPP processing Journal:Nature	Yu, G Nishimura, M Arawaka, S Levitan, D Zhang, L Tandon, A Song, YQ Rogaeva, E Chen, F Kawarai, T Supala, A Levesque, L Yu, H Yang, DS Holmes, E Milman, P Liang, Y Zhang, DM Xu, DH Sato, C Rogaev, E Smith, M Janus, C Zhang, Y Aebersold, R Farrer, L Sorbl, S Bruni, A Fraser, P GeorgeHyslop, PS	2000	155
	PS1 Alzheimer's disease family with spastic paraplegia: The search for a gene modifier Journal:Neurology	Rogaeva, E Bergeron, C Sato, C Moliaka, I Kawarai, T Toulina, A Song, YQ Kolesnikova, T Orlacchio, A Bernardi, G St GeorgeHyslop, PH	2003	136
	The sortilin-related recentor SORLA is functionally and genetically associated with Alzheimer Disease Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2005	Meng, Y Rogaeva, E Lee, JH Gu, YJ Kawarai, T Katayama, T Erlich, P Baldwin, CT Cheng, R Hasegawa, H Chen, F Shibata, N Lunetta, KL Cupples, LA Song, Y Fraser, PE Westaway, D Mayeux, R Farrer, LA St. George-Hyslop, P	2005	132
	The sortilin-related receptor SORL1 is genetically associated with Alzheimer’s 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 Song, Y Fraser, PE Schmitt-Ulms, G Younkin, S Mayeux, R Farrer, LA St George-Hyslop, P	2007	71
	An α-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease [5] (multiple letters) Journal:Nature Genetics	Rogaeva, EA Premkumar, S Grubber, J Serneels, L Scott, WK Kawarai, T Song, Y Hill, DM AbouDonia, SM Martin, ER Vance, JJ Yu, G Orlacchio, A Pei, Y Nishimura, M Supala, A Roberge, B Saunders, AM Roses, AD Schmechel, D CraneGatherum, A Sorbi, S Bruni, A Small, GW Conneally, PM Haines, JL Van Leuven, F St GeorgeHyslop, PH Farrer, LA Pericak Vance, MA Blacker, D Crystal, AS Wilcox, MA Laird, NM Tanzi, RE	1999	139

Showing results 6 to 19 of 19 < previous