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P H St George-Hyslop

Showing results (11-20 of 72) with videos related to

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Neuroscience Letters|May 4, 2000
Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigreesA Orlacchio, T Kawarai, A M Massaro, et al.
Brain Research. Molecular Brain Research|February 1, 1995
Beta APP mRNA transcription is increased in cultured fibroblasts from the familial Alzheimer's disease-1 familyH W Querfurth, E M Wijsman, P H St George-Hyslop, et al.
Genomics|July 15, 1994
The upstream promoter of the beta-amyloid precursor protein gene (APP) shows differential patterns of methylation in human brainE I Rogaev, W J Lukiw, O Lavrushina, et al.
The Journal of Biological Chemistry|May 10, 2000
Inhibiting amyloid precursor protein C-terminal cleavage promotes an interaction with presenilin 1G Verdile, R N Martins, M Duthie, et al.
Neurology|May 26, 2004
A new SPG4 mutation in a variant form of spastic paraplegia with congenital arachnoid cystsA Orlacchio, F Gaudiello, A Totaro, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|September 23, 1998
Age-related changes in D2 receptor binding with iodine-123-iodobenzofuran SPECTM Ichise, J R Ballinger, F Tanaka, et al.
Neurology|November 13, 2002
Clinical and genetic study of a large Italian family linked to SPG12 locusA Orlacchio, T Kawarai, E Rogaeva, et al.
Neurology|November 1, 1995
Variable clinical symptoms in familial amyotrophic lateral sclerosis with a novel point mutation in the Cu/Zn superoxide dismutase geneM Ikeda, K Abe, M Aoki, et al.
Neurology|April 1, 1997
A presenilin-1 mutation in a Japanese family with Alzheimer's disease and distinctive abnormalities on cranial MRIM Aoki, K Abe, N Oda, et al.
Acta Neuropathologica|September 29, 1999
Glial expression of presenilin epitopes in human brain with cerebral infarction and in astrocytomaH Miake, K Tsuchiya, A Nakamura, et al.
Pageof 8

Showing results (11-20 of 72) with videos related to

Sort By:
Pageof 8
Neuroscience Letters|May 4, 2000
Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigreesA Orlacchio, T Kawarai, A M Massaro, et al.
Brain Research. Molecular Brain Research|February 1, 1995
Beta APP mRNA transcription is increased in cultured fibroblasts from the familial Alzheimer's disease-1 familyH W Querfurth, E M Wijsman, P H St George-Hyslop, et al.
Genomics|July 15, 1994
The upstream promoter of the beta-amyloid precursor protein gene (APP) shows differential patterns of methylation in human brainE I Rogaev, W J Lukiw, O Lavrushina, et al.
The Journal of Biological Chemistry|May 10, 2000
Inhibiting amyloid precursor protein C-terminal cleavage promotes an interaction with presenilin 1G Verdile, R N Martins, M Duthie, et al.
Neurology|May 26, 2004
A new SPG4 mutation in a variant form of spastic paraplegia with congenital arachnoid cystsA Orlacchio, F Gaudiello, A Totaro, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|September 23, 1998
Age-related changes in D2 receptor binding with iodine-123-iodobenzofuran SPECTM Ichise, J R Ballinger, F Tanaka, et al.
Neurology|November 13, 2002
Clinical and genetic study of a large Italian family linked to SPG12 locusA Orlacchio, T Kawarai, E Rogaeva, et al.
Neurology|November 1, 1995
Variable clinical symptoms in familial amyotrophic lateral sclerosis with a novel point mutation in the Cu/Zn superoxide dismutase geneM Ikeda, K Abe, M Aoki, et al.
Neurology|April 1, 1997
A presenilin-1 mutation in a Japanese family with Alzheimer's disease and distinctive abnormalities on cranial MRIM Aoki, K Abe, N Oda, et al.
Acta Neuropathologica|September 29, 1999
Glial expression of presenilin epitopes in human brain with cerebral infarction and in astrocytomaH Miake, K Tsuchiya, A Nakamura, et al.
Pageof 8