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G D Schellenberg

Showing results (41-50 of 128) with videos related to

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Genomics|August 1, 1996
A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21C E Yu, J Oshima, F M Hisama, et al.
Neurology|March 27, 2002
HLA-A2 homozygosity but not heterozygosity is associated with Alzheimer diseaseS Zareparsi, D M James, J A Kaye, et al.
Annals of Neurology|February 1, 1992
Genetic association and linkage analysis of the apolipoprotein CII locus and familial Alzheimer's diseaseG D Schellenberg, M Boehnke, E M Wijsman, et al.
Neurology|June 1, 1995
Interactions of apolipoprotein E genotype, total cholesterol level, age, and sex in prediction of Alzheimer's disease: a case-control studyG P Jarvik, E M Wijsman, W A Kukull, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 13, 1999
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elementsI D'Souza, P Poorkaj, M Hong, et al.
Genomics|June 1, 1996
Genomic structure and expression of STM2, the chromosome 1 familial Alzheimer disease geneE Levy-Lahad, P Poorkaj, K Wang, et al.
Neurology|June 20, 1998
Midlife cardiovascular risk factors, ApoE, and cognitive decline in elderly male twinsD Carmelli, G E Swan, T Reed, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 23, 2003
Apolipoprotein E genotypes and outcome from out of hospital cardiac arrestW T Longstreth, G D Schellenberg, C E Fahrenbruch, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 20, 2001
A genomic sequence analysis of the mouse and human microtubule-associated protein tauP Poorkaj, A Kas, I D'Souza, et al.
Pharmacogenetics|July 18, 2000
Analysis of paraoxonase (PON1) L55M status requires both genotype and phenotypeV H Brophy, G P Jarvik, R J Richter, et al.
Pageof 13

Showing results (41-50 of 128) with videos related to

Sort By:
Pageof 13
Genomics|August 1, 1996
A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21C E Yu, J Oshima, F M Hisama, et al.
Neurology|March 27, 2002
HLA-A2 homozygosity but not heterozygosity is associated with Alzheimer diseaseS Zareparsi, D M James, J A Kaye, et al.
Annals of Neurology|February 1, 1992
Genetic association and linkage analysis of the apolipoprotein CII locus and familial Alzheimer's diseaseG D Schellenberg, M Boehnke, E M Wijsman, et al.
Neurology|June 1, 1995
Interactions of apolipoprotein E genotype, total cholesterol level, age, and sex in prediction of Alzheimer's disease: a case-control studyG P Jarvik, E M Wijsman, W A Kukull, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 13, 1999
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elementsI D'Souza, P Poorkaj, M Hong, et al.
Genomics|June 1, 1996
Genomic structure and expression of STM2, the chromosome 1 familial Alzheimer disease geneE Levy-Lahad, P Poorkaj, K Wang, et al.
Neurology|June 20, 1998
Midlife cardiovascular risk factors, ApoE, and cognitive decline in elderly male twinsD Carmelli, G E Swan, T Reed, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 23, 2003
Apolipoprotein E genotypes and outcome from out of hospital cardiac arrestW T Longstreth, G D Schellenberg, C E Fahrenbruch, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 20, 2001
A genomic sequence analysis of the mouse and human microtubule-associated protein tauP Poorkaj, A Kas, I D'Souza, et al.
Pharmacogenetics|July 18, 2000
Analysis of paraoxonase (PON1) L55M status requires both genotype and phenotypeV H Brophy, G P Jarvik, R J Richter, et al.
Pageof 13