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H Backhovens

Showing results (31-40 of 42) with videos related to

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Annals of Neurology|July 1, 1997
Presenilin-1 polymorphism and hereditary cerebral hemorrhage with amyloidosis, Dutch typeM Bornebroek, J Haan, H Backhovens, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
Genetic association of the presenilin-1 regulatory region with early-onset Alzheimer's disease in a population-based sampleC M van Duijn, M Cruts, J Theuns, et al.
Human Molecular Genetics|December 1, 1995
Molecular genetic analysis of familial early-onset Alzheimer's disease linked to chromosome 14q24.3M Cruts, H Backhovens, S Y Wang, et al.
Neuroscience Letters|January 7, 2000
Mutation screening of the tau gene in patients with early-onset Alzheimer's diseaseG Roks, B Dermaut, P Heutink, et al.
Molecular Psychiatry|December 12, 2002
Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM intervalR Rademakers, M Cruts, B Dermaut, et al.
Human Molecular Genetics|February 3, 2000
Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expressionJ Theuns, J Del-Favero, B Dermaut, et al.
Molecular Psychiatry|January 31, 2003
A novel CpG-associated brain-expressed candidate gene for chromosome 18q-linked bipolar disorderD Goossens, S Van Gestel, S Claes, et al.
Human Molecular Genetics|March 21, 1998
Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansionJ Del-Favero, L Krols, A Michalik, et al.
Human Molecular Genetics|February 28, 1998
Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer diseaseM Cruts, C M van Duijn, H Backhovens, et al.
Human Molecular Genetics|November 7, 2000
Nonfibrillar diffuse amyloid deposition due to a gamma(42)-secretase site mutation points to an essential role for N-truncated A beta(42) in Alzheimer's diseaseS Kumar-Singh, C De Jonghe, M Cruts, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Annals of Neurology|July 1, 1997
Presenilin-1 polymorphism and hereditary cerebral hemorrhage with amyloidosis, Dutch typeM Bornebroek, J Haan, H Backhovens, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
Genetic association of the presenilin-1 regulatory region with early-onset Alzheimer's disease in a population-based sampleC M van Duijn, M Cruts, J Theuns, et al.
Human Molecular Genetics|December 1, 1995
Molecular genetic analysis of familial early-onset Alzheimer's disease linked to chromosome 14q24.3M Cruts, H Backhovens, S Y Wang, et al.
Neuroscience Letters|January 7, 2000
Mutation screening of the tau gene in patients with early-onset Alzheimer's diseaseG Roks, B Dermaut, P Heutink, et al.
Molecular Psychiatry|December 12, 2002
Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM intervalR Rademakers, M Cruts, B Dermaut, et al.
Human Molecular Genetics|February 3, 2000
Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expressionJ Theuns, J Del-Favero, B Dermaut, et al.
Molecular Psychiatry|January 31, 2003
A novel CpG-associated brain-expressed candidate gene for chromosome 18q-linked bipolar disorderD Goossens, S Van Gestel, S Claes, et al.
Human Molecular Genetics|March 21, 1998
Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansionJ Del-Favero, L Krols, A Michalik, et al.
Human Molecular Genetics|February 28, 1998
Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer diseaseM Cruts, C M van Duijn, H Backhovens, et al.
Human Molecular Genetics|November 7, 2000
Nonfibrillar diffuse amyloid deposition due to a gamma(42)-secretase site mutation points to an essential role for N-truncated A beta(42) in Alzheimer's diseaseS Kumar-Singh, C De Jonghe, M Cruts, et al.
Pageof 5