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P St George-Hyslop

Showing results (61-70 of 85) with videos related to

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Neurobiology of Disease|January 1, 1997
Presenilin proteins undergo heterogeneous endoproteolysis between Thr291 and Ala299 and occur as stable N- and C-terminal fragments in normal and Alzheimer brain tissueM B Podlisny, M Citron, P Amarante, et al.
Acta Neurologica Scandinavica. Supplementum|March 23, 2001
Mutation of conserved aspartates affect maturation of presenilin 1 and presenilin 2 complexesG Yu, F Chen, M Nishimura, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 20, 1996
Conservation of synteny between the genome of the pufferfish (Fugu rubripes) and the region on human chromosome 14 (14q24.3) associated with familial Alzheimer disease (AD3 locus)M K Trower, S M Orton, I J Purvis, et al.
The Journal of Biological Chemistry|October 14, 2000
Increased production of beta-amyloid and vulnerability to endoplasmic reticulum stress by an aberrant spliced form of presenilin 2N Sato, K Imaizumi, T Manabe, et al.
Genomics|March 15, 1997
Analysis of the 5' sequence, genomic structure, and alternative splicing of the presenilin-1 gene (PSEN1) associated with early onset Alzheimer diseaseE I Rogaev, R Sherrington, C Wu, et al.
Neuroreport|October 24, 2000
Mutation of the conserved N-terminal cysteine (Cys92) of human presenilin 1 causes increased A beta42 secretion in mammalian cells but impaired Notch/lin-12 signalling in C. elegansD M Zhang, D Levitan, G Yu, et al.
Neurology|August 29, 2001
Screening for PS1 mutations in a referral-based series of AD cases: 21 novel mutationsE A Rogaeva, K C Fafel, Y Q Song, et al.
Neuroscience Letters|August 26, 1998
Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOEY Q Song, E Rogaeva, S Premkumar, et al.
Nature Cell Biology|December 10, 1999
Presenilin-1 mutations downregulate the signalling pathway of the unfolded-protein responseT Katayama, K Imaizumi, N Sato, et al.
European Journal of Neurology|August 30, 2008
A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairmentS G Lindquist, L Hasholt, J M C Bahl, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
Neurobiology of Disease|January 1, 1997
Presenilin proteins undergo heterogeneous endoproteolysis between Thr291 and Ala299 and occur as stable N- and C-terminal fragments in normal and Alzheimer brain tissueM B Podlisny, M Citron, P Amarante, et al.
Acta Neurologica Scandinavica. Supplementum|March 23, 2001
Mutation of conserved aspartates affect maturation of presenilin 1 and presenilin 2 complexesG Yu, F Chen, M Nishimura, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 20, 1996
Conservation of synteny between the genome of the pufferfish (Fugu rubripes) and the region on human chromosome 14 (14q24.3) associated with familial Alzheimer disease (AD3 locus)M K Trower, S M Orton, I J Purvis, et al.
The Journal of Biological Chemistry|October 14, 2000
Increased production of beta-amyloid and vulnerability to endoplasmic reticulum stress by an aberrant spliced form of presenilin 2N Sato, K Imaizumi, T Manabe, et al.
Genomics|March 15, 1997
Analysis of the 5' sequence, genomic structure, and alternative splicing of the presenilin-1 gene (PSEN1) associated with early onset Alzheimer diseaseE I Rogaev, R Sherrington, C Wu, et al.
Neuroreport|October 24, 2000
Mutation of the conserved N-terminal cysteine (Cys92) of human presenilin 1 causes increased A beta42 secretion in mammalian cells but impaired Notch/lin-12 signalling in C. elegansD M Zhang, D Levitan, G Yu, et al.
Neurology|August 29, 2001
Screening for PS1 mutations in a referral-based series of AD cases: 21 novel mutationsE A Rogaeva, K C Fafel, Y Q Song, et al.
Neuroscience Letters|August 26, 1998
Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOEY Q Song, E Rogaeva, S Premkumar, et al.
Nature Cell Biology|December 10, 1999
Presenilin-1 mutations downregulate the signalling pathway of the unfolded-protein responseT Katayama, K Imaizumi, N Sato, et al.
European Journal of Neurology|August 30, 2008
A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairmentS G Lindquist, L Hasholt, J M C Bahl, et al.
Pageof 9