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Showing results (11-20 of 80) with videos related to

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Human Mutation|October 1, 2003
Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in Western EuropeR Rademakers, B Dermaut, K Peeters, et al.
Neurology|December 17, 1998
Mutation, sequence analysis, and association studies of alpha-synuclein in Parkinson's diseaseA Parsian, B Racette, Z H Zhang, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Genetic characterization of a novel familial dementiaJ Brown, S Smith, A Brun, et al.
Neurology|August 12, 2009
Presenilin1 G217R mutation linked to Alzheimer disease with cotton wool plaquesJ B Norton, N J Cairns, S Chakraverty, et al.
Neuroscience Letters|November 25, 1991
Sequencing of exons 16 and 17 of the beta-amyloid precursor protein gene in 14 families with early onset Alzheimer's disease fails to reveal mutations in the beta-amyloid sequenceF Crawford, J Hardy, M Mullan, et al.
Alcoholism, Clinical and Experimental Research|April 6, 2001
A genome-wide search for genes that relate to a low level of response to alcoholM A Schuckit, H J Edenberg, J Kalmijn, et al.
Neuroreport|January 31, 1996
Polymorphism in AACT gene may lower age of onset of Alzheimer's diseaseC Talbot, H Houlden, N Craddock, et al.
Dementia (Basel, Switzerland)|May 1, 1993
Exclusion mapping in familial non-specific dementiaJ Brown, S Gydesen, S A Sorensen, et al.
Human Molecular Genetics|June 1, 1992
Screening for mutations in the open reading frame and promoter of the beta-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val-->IleL Fidani, K Rooke, M C Chartier-Harlin, et al.
Neuroscience Letters|August 5, 1991
Screening for the beta-amyloid precursor protein mutation (APP717: Val----Ile) in extended pedigrees with early onset Alzheimer's diseaseM C Chartier-Harlin, F Crawford, K Hamandi, et al.
Pageof 8

Showing results (11-20 of 80) with videos related to

Sort By:
Pageof 8
Human Mutation|October 1, 2003
Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in Western EuropeR Rademakers, B Dermaut, K Peeters, et al.
Neurology|December 17, 1998
Mutation, sequence analysis, and association studies of alpha-synuclein in Parkinson's diseaseA Parsian, B Racette, Z H Zhang, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Genetic characterization of a novel familial dementiaJ Brown, S Smith, A Brun, et al.
Neurology|August 12, 2009
Presenilin1 G217R mutation linked to Alzheimer disease with cotton wool plaquesJ B Norton, N J Cairns, S Chakraverty, et al.
Neuroscience Letters|November 25, 1991
Sequencing of exons 16 and 17 of the beta-amyloid precursor protein gene in 14 families with early onset Alzheimer's disease fails to reveal mutations in the beta-amyloid sequenceF Crawford, J Hardy, M Mullan, et al.
Alcoholism, Clinical and Experimental Research|April 6, 2001
A genome-wide search for genes that relate to a low level of response to alcoholM A Schuckit, H J Edenberg, J Kalmijn, et al.
Neuroreport|January 31, 1996
Polymorphism in AACT gene may lower age of onset of Alzheimer's diseaseC Talbot, H Houlden, N Craddock, et al.
Dementia (Basel, Switzerland)|May 1, 1993
Exclusion mapping in familial non-specific dementiaJ Brown, S Gydesen, S A Sorensen, et al.
Human Molecular Genetics|June 1, 1992
Screening for mutations in the open reading frame and promoter of the beta-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val-->IleL Fidani, K Rooke, M C Chartier-Harlin, et al.
Neuroscience Letters|August 5, 1991
Screening for the beta-amyloid precursor protein mutation (APP717: Val----Ile) in extended pedigrees with early onset Alzheimer's diseaseM C Chartier-Harlin, F Crawford, K Hamandi, et al.
Pageof 8