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P St George-Hyslop

Showing results (21-30 of 85) with videos related to

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Molecular Medicine (Cambridge, Mass.)|September 21, 2000
Evidence that the beta-catenin nuclear translocation assay allows for measuring presenilin 1 dysfunctionG Van Gassen, C De Jonghe, M Nishimura, et al.
Neurology|February 20, 1999
A cross-ethnic analysis of risk factors for AD in white Hispanics and white non-HispanicsD G Harwood, W W Barker, D A Loewenstein, et al.
Science (New York, N.Y.)|January 28, 1994
Alzheimer's disease and possible gene interactionP St George-Hyslop, D C McLachlan, T Tsuda, et al.
Human Molecular Genetics|May 1, 1993
A highly informative microsatellite repeat polymorphism in intron 1 of the human amyloid precursor protein (APP) geneR Tupler, E Rogaeva, G Vaula, et al.
Neurology|July 27, 2005
Familial Alzheimer disease: decreases in CSF Abeta42 levels precede cognitive declineM Moonis, J M Swearer, M P E Dayaw, et al.
Nature Genetics|June 3, 2000
Mutations of PKD1 in ADPKD2 cysts suggest a pathogenic effect of trans-heterozygous mutationsT Watnick, N He, K Wang, et al.
Free Radical Biology & Medicine|June 25, 1999
Expression of human FALS SOD in motorneurons of DrosophilaA J Elia, T L Parkes, K Kirby, et al.
Journal of Neural Transmission. Supplementum|January 1, 1987
Search for the familial Alzheimer's disease geneP St George-Hyslop, R Polinsky, J Haines, et al.
Science (New York, N.Y.)|April 17, 1987
Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosisB R Seizinger, G Rouleau, L J Ozelius, et al.
Kidney International|May 9, 1998
A novel frameshift mutation induced by an adenosine insertion in the polycystic kidney disease 2 (PKD2) geneY Pei, K Wang, M Kasenda, et al.
Pageof 9

Showing results (21-30 of 85) with videos related to

Sort By:
Pageof 9
Molecular Medicine (Cambridge, Mass.)|September 21, 2000
Evidence that the beta-catenin nuclear translocation assay allows for measuring presenilin 1 dysfunctionG Van Gassen, C De Jonghe, M Nishimura, et al.
Neurology|February 20, 1999
A cross-ethnic analysis of risk factors for AD in white Hispanics and white non-HispanicsD G Harwood, W W Barker, D A Loewenstein, et al.
Science (New York, N.Y.)|January 28, 1994
Alzheimer's disease and possible gene interactionP St George-Hyslop, D C McLachlan, T Tsuda, et al.
Human Molecular Genetics|May 1, 1993
A highly informative microsatellite repeat polymorphism in intron 1 of the human amyloid precursor protein (APP) geneR Tupler, E Rogaeva, G Vaula, et al.
Neurology|July 27, 2005
Familial Alzheimer disease: decreases in CSF Abeta42 levels precede cognitive declineM Moonis, J M Swearer, M P E Dayaw, et al.
Nature Genetics|June 3, 2000
Mutations of PKD1 in ADPKD2 cysts suggest a pathogenic effect of trans-heterozygous mutationsT Watnick, N He, K Wang, et al.
Free Radical Biology & Medicine|June 25, 1999
Expression of human FALS SOD in motorneurons of DrosophilaA J Elia, T L Parkes, K Kirby, et al.
Journal of Neural Transmission. Supplementum|January 1, 1987
Search for the familial Alzheimer's disease geneP St George-Hyslop, R Polinsky, J Haines, et al.
Science (New York, N.Y.)|April 17, 1987
Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosisB R Seizinger, G Rouleau, L J Ozelius, et al.
Kidney International|May 9, 1998
A novel frameshift mutation induced by an adenosine insertion in the polycystic kidney disease 2 (PKD2) geneY Pei, K Wang, M Kasenda, et al.
Pageof 9