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Showing results 4 to 11 of 11 < previous

	Title	Author(s)	Issue Date
	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
	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
	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
	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
	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
	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
	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
	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 4 to 11 of 11 < previous