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M Cruts

Showing results (31-40 of 80) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 24, 1999
Determination of the genomic organization of human presenilin 1 by fiber-FISH analysis and restriction mapping of cloned DNAJ Theuns, M Cruts, J Del-Favero, et al.
American Journal of Human Genetics|October 1, 1994
A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21C M van Duijn, L Hendriks, L A Farrer, et al.
Human Mutation|April 13, 1999
Missense mutation in exon 11 (Codon 378) of the presenilin-1 gene in a French family with early-onset Alzheimer's disease and transmission study by mismatch enhanced allele specific amplification. Mutations in brief no. 141. Online. besancon@rockefeller1.univ.lyon1.frR Besançon, A Lorenzi, M Cruts, et al.
Neuroscience Letters|November 8, 2001
The microtubule associated protein Tau gene and Alzheimer's disease--an association study and meta-analysisC Russ, J F Powell, J Zhao, et al.
Neuroscience Letters|October 31, 2001
Amyloid beta secretase gene (BACE) is neither mutated in nor associated with early-onset Alzheimer's diseaseM Cruts, B Dermaut, R Rademakers, et al.
Human Molecular Genetics|August 1, 1995
Genetic and physical characterization of the early-onset Alzheimer's disease AD3 locus on chromosome 14q24.3M Cruts, H Backhovens, J Theuns, et al.
Journal of Neurology|July 15, 2000
Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertionB Dermaut, M Cruts, H Backhovens, et al.
American Journal of Human Genetics|June 23, 1998
Genetic association of apolipoprotein E with age-related macular degenerationC C Klaver, M Kliffen, C M van Duijn, et al.
Neurobiology of Disease|August 17, 1999
Evidence that Abeta42 plasma levels in presenilin-1 mutation carriers do not allow for prediction of their clinical phenotypeC De Jonghe, P Cras, H Vanderstichele, et al.
Neuroscience Letters|July 17, 1998
Serum apolipoprotein E level is not increased in Alzheimer's disease: the Rotterdam studyA J Slooter, P de Knijff, A Hofman, et al.
Pageof 8

Showing results (31-40 of 80) with videos related to

Sort By:
Pageof 8
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 24, 1999
Determination of the genomic organization of human presenilin 1 by fiber-FISH analysis and restriction mapping of cloned DNAJ Theuns, M Cruts, J Del-Favero, et al.
American Journal of Human Genetics|October 1, 1994
A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21C M van Duijn, L Hendriks, L A Farrer, et al.
Human Mutation|April 13, 1999
Missense mutation in exon 11 (Codon 378) of the presenilin-1 gene in a French family with early-onset Alzheimer's disease and transmission study by mismatch enhanced allele specific amplification. Mutations in brief no. 141. Online. besancon@rockefeller1.univ.lyon1.frR Besançon, A Lorenzi, M Cruts, et al.
Neuroscience Letters|November 8, 2001
The microtubule associated protein Tau gene and Alzheimer's disease--an association study and meta-analysisC Russ, J F Powell, J Zhao, et al.
Neuroscience Letters|October 31, 2001
Amyloid beta secretase gene (BACE) is neither mutated in nor associated with early-onset Alzheimer's diseaseM Cruts, B Dermaut, R Rademakers, et al.
Human Molecular Genetics|August 1, 1995
Genetic and physical characterization of the early-onset Alzheimer's disease AD3 locus on chromosome 14q24.3M Cruts, H Backhovens, J Theuns, et al.
Journal of Neurology|July 15, 2000
Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertionB Dermaut, M Cruts, H Backhovens, et al.
American Journal of Human Genetics|June 23, 1998
Genetic association of apolipoprotein E with age-related macular degenerationC C Klaver, M Kliffen, C M van Duijn, et al.
Neurobiology of Disease|August 17, 1999
Evidence that Abeta42 plasma levels in presenilin-1 mutation carriers do not allow for prediction of their clinical phenotypeC De Jonghe, P Cras, H Vanderstichele, et al.
Neuroscience Letters|July 17, 1998
Serum apolipoprotein E level is not increased in Alzheimer's disease: the Rotterdam studyA J Slooter, P de Knijff, A Hofman, et al.
Pageof 8