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P St George-Hyslop

Showing results (51-60 of 85) with videos related to

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Annals of Neurology|September 8, 2000
Familial Alzheimer's disease: site of mutation influences clinical phenotypeC F Lippa, J M Swearer, K J Kane, et al.
Archives of Neurology|October 13, 2000
Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer diseaseG Devi, A Fotiou, D Jyrinji, et al.
Human Molecular Genetics|May 1, 1996
Linkage of polymorphic congenital cataract to the gamma-crystallin gene locus on human chromosome 2q33-35E I Rogaev, E A Rogaeva, G I Korovaitseva, et al.
Journal of the American Society of Nephrology : JASN|October 17, 1998
A spectrum of mutations in the polycystic kidney disease-2 (PKD2) gene from eight Canadian kindredsY Pei, N He, K Wang, et al.
Science (New York, N.Y.)|February 20, 1987
Amyloid beta protein gene: cDNA, mRNA distribution, and genetic linkage near the Alzheimer locusR E Tanzi, J F Gusella, P C Watkins, et al.
Molecular Medicine (Cambridge, Mass.)|September 29, 1999
Developmental expression of wild-type and mutant presenilin-1 in hippocampal neurons from transgenic mice: evidence for novel species-specific properties of human presenilin-1L Lévesque, W Annaert, K Craessaerts, et al.
Archives of General Psychiatry|February 11, 1992
Psychiatric, genetic, and positron emission tomographic evaluation of persons at risk for Huntington's diseaseL R Baxter, J C Mazziotta, J J Pahl, et al.
Molecular Psychiatry|March 3, 2004
Baculoviruses expressing the human familial Alzheimer's disease presenilin 1 mutation lacking exon 9 increase levels of an amyloid beta-like protein in Sf9 cellsG Verdile, D Groth, P M Mathews, et al.
Neurobiology of Aging|January 24, 2002
Normal brain development in PS1 hypomorphic mice with markedly reduced gamma-secretase cleavage of betaAPPR Rozmahel, J Huang, F Chen, et al.
Dementia and Geriatric Cognitive Disorders|September 9, 2006
Intron 2 (T/C) CYP46 polymorphism is associated with Alzheimer's disease in Chinese patientsY Li, L W Chu, Y Q Chen, et al.
Pageof 9

Showing results (51-60 of 85) with videos related to

Sort By:
Pageof 9
Annals of Neurology|September 8, 2000
Familial Alzheimer's disease: site of mutation influences clinical phenotypeC F Lippa, J M Swearer, K J Kane, et al.
Archives of Neurology|October 13, 2000
Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer diseaseG Devi, A Fotiou, D Jyrinji, et al.
Human Molecular Genetics|May 1, 1996
Linkage of polymorphic congenital cataract to the gamma-crystallin gene locus on human chromosome 2q33-35E I Rogaev, E A Rogaeva, G I Korovaitseva, et al.
Journal of the American Society of Nephrology : JASN|October 17, 1998
A spectrum of mutations in the polycystic kidney disease-2 (PKD2) gene from eight Canadian kindredsY Pei, N He, K Wang, et al.
Science (New York, N.Y.)|February 20, 1987
Amyloid beta protein gene: cDNA, mRNA distribution, and genetic linkage near the Alzheimer locusR E Tanzi, J F Gusella, P C Watkins, et al.
Molecular Medicine (Cambridge, Mass.)|September 29, 1999
Developmental expression of wild-type and mutant presenilin-1 in hippocampal neurons from transgenic mice: evidence for novel species-specific properties of human presenilin-1L Lévesque, W Annaert, K Craessaerts, et al.
Archives of General Psychiatry|February 11, 1992
Psychiatric, genetic, and positron emission tomographic evaluation of persons at risk for Huntington's diseaseL R Baxter, J C Mazziotta, J J Pahl, et al.
Molecular Psychiatry|March 3, 2004
Baculoviruses expressing the human familial Alzheimer's disease presenilin 1 mutation lacking exon 9 increase levels of an amyloid beta-like protein in Sf9 cellsG Verdile, D Groth, P M Mathews, et al.
Neurobiology of Aging|January 24, 2002
Normal brain development in PS1 hypomorphic mice with markedly reduced gamma-secretase cleavage of betaAPPR Rozmahel, J Huang, F Chen, et al.
Dementia and Geriatric Cognitive Disorders|September 9, 2006
Intron 2 (T/C) CYP46 polymorphism is associated with Alzheimer's disease in Chinese patientsY Li, L W Chu, Y Q Chen, et al.
Pageof 9