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P H St George-Hyslop

Showing results (51-60 of 72) with videos related to

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Neurology|May 5, 1998
Gender-related penetrance and de novo GTP-cyclohydrolase I gene mutations in dopa-responsive dystoniaY Furukawa, A E Lang, J M Trugman, et al.
Brain Research|February 14, 1997
Abeta1-40 but not Abeta1-42 levels in cortex correlate with apolipoprotein E epsilon4 allele dosage in sporadic Alzheimer's diseaseK Ishii, A Tamaoka, H Mizusawa, et al.
Molecular Psychiatry|August 23, 2002
Association between presenilin-1 Glu318Gly mutation and familial Alzheimer's disease in the Australian populationK Taddei, C Fisher, S M Laws, et al.
Human Molecular Genetics|July 13, 1999
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretionC De Jonghe, M Cruts, E A Rogaeva, et al.
JAMA|August 26, 1998
Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneityE Rogaeva, S Premkumar, Y Song, et al.
Nature Cell Biology|August 3, 2001
Nicastrin binds to membrane-tethered NotchF Chen, G Yu, S Arawaka, et al.
Annals of Neurology|December 1, 1996
The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patientsM Ikeda, V Sharma, S M Sumi, et al.
Neurobiology of Aging|May 21, 2005
The effects of APOE and tau gene variability on risk of frontotemporal dementiaL Bernardi, R G Maletta, C Tomaino, et al.
FEBS Letters|December 31, 1997
Proteolytic processing of presenilin-1 (PS-1) is not associated with Alzheimer's disease with or without PS-1 mutationsM Okochi, K Ishii, M Usami, et al.
Neuroreport|April 14, 1997
Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotypeJ B Kwok, K Taddei, M Hallupp, et al.
Pageof 8

Showing results (51-60 of 72) with videos related to

Sort By:
Pageof 8
Neurology|May 5, 1998
Gender-related penetrance and de novo GTP-cyclohydrolase I gene mutations in dopa-responsive dystoniaY Furukawa, A E Lang, J M Trugman, et al.
Brain Research|February 14, 1997
Abeta1-40 but not Abeta1-42 levels in cortex correlate with apolipoprotein E epsilon4 allele dosage in sporadic Alzheimer's diseaseK Ishii, A Tamaoka, H Mizusawa, et al.
Molecular Psychiatry|August 23, 2002
Association between presenilin-1 Glu318Gly mutation and familial Alzheimer's disease in the Australian populationK Taddei, C Fisher, S M Laws, et al.
Human Molecular Genetics|July 13, 1999
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretionC De Jonghe, M Cruts, E A Rogaeva, et al.
JAMA|August 26, 1998
Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneityE Rogaeva, S Premkumar, Y Song, et al.
Nature Cell Biology|August 3, 2001
Nicastrin binds to membrane-tethered NotchF Chen, G Yu, S Arawaka, et al.
Annals of Neurology|December 1, 1996
The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patientsM Ikeda, V Sharma, S M Sumi, et al.
Neurobiology of Aging|May 21, 2005
The effects of APOE and tau gene variability on risk of frontotemporal dementiaL Bernardi, R G Maletta, C Tomaino, et al.
FEBS Letters|December 31, 1997
Proteolytic processing of presenilin-1 (PS-1) is not associated with Alzheimer's disease with or without PS-1 mutationsM Okochi, K Ishii, M Usami, et al.
Neuroreport|April 14, 1997
Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotypeJ B Kwok, K Taddei, M Hallupp, et al.
Pageof 8