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D Schellenberg

Showing results (181-190 of 503) with videos related to

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Nucleic Acids Research|August 17, 2018
INFERNO: inferring the molecular mechanisms of noncoding genetic variantsAlexandre Amlie-Wolf, Mitchell Tang, Elisabeth E Mlynarski, et al.
Journal of Clinical Epidemiology|October 1, 1996
Apolipoprotein E in Alzheimer's disease risk and case detection: a case-control studyW A Kukull, G D Schellenberg, J D Bowen, et al.
Genomics|April 17, 2007
Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker associationChang-En Yu, Howard Seltman, Elaine R Peskind, et al.
Journal of Neurochemistry|September 27, 2003
Alteration in calcium channel properties is responsible for the neurotoxic action of a familial frontotemporal dementia tau mutationKatsutoshi Furukawa, Yue Wang, Pamela J Yao, et al.
Archives of Neurology|March 15, 2006
Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotypeJames B Leverenz, Mark A Fishel, Elaine R Peskind, et al.
Science (New York, N.Y.)|October 23, 1992
Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14G D Schellenberg, T D Bird, E M Wijsman, et al.
Tropical Medicine & International Health : TM & IH|September 3, 2003
An estimation of the entomological inoculation rate for Ifakara: a semi-urban area in a region of intense malaria transmission in TanzaniaC Drakeley, D Schellenberg, J Kihonda, et al.
American Journal of Human Genetics|September 1, 1993
Chromosome 14 and late-onset familial Alzheimer disease (FAD)G D Schellenberg, H Payami, E M Wijsman, et al.
Clinical Oncology (Royal College of Radiologists (Great Britain))|February 23, 2019
Stereotactic Body Radiotherapy for Small Unresectable Hepatocellular CarcinomasR Yeung, L Beaton, T Rackley, et al.
American Journal of Human Genetics|February 1, 1997
Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative GroupC E Yu, J Oshima, E M Wijsman, et al.
Pageof 51

Showing results (181-190 of 503) with videos related to

Sort By:
Pageof 51
Nucleic Acids Research|August 17, 2018
INFERNO: inferring the molecular mechanisms of noncoding genetic variantsAlexandre Amlie-Wolf, Mitchell Tang, Elisabeth E Mlynarski, et al.
Journal of Clinical Epidemiology|October 1, 1996
Apolipoprotein E in Alzheimer's disease risk and case detection: a case-control studyW A Kukull, G D Schellenberg, J D Bowen, et al.
Genomics|April 17, 2007
Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker associationChang-En Yu, Howard Seltman, Elaine R Peskind, et al.
Journal of Neurochemistry|September 27, 2003
Alteration in calcium channel properties is responsible for the neurotoxic action of a familial frontotemporal dementia tau mutationKatsutoshi Furukawa, Yue Wang, Pamela J Yao, et al.
Archives of Neurology|March 15, 2006
Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotypeJames B Leverenz, Mark A Fishel, Elaine R Peskind, et al.
Science (New York, N.Y.)|October 23, 1992
Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14G D Schellenberg, T D Bird, E M Wijsman, et al.
Tropical Medicine & International Health : TM & IH|September 3, 2003
An estimation of the entomological inoculation rate for Ifakara: a semi-urban area in a region of intense malaria transmission in TanzaniaC Drakeley, D Schellenberg, J Kihonda, et al.
American Journal of Human Genetics|September 1, 1993
Chromosome 14 and late-onset familial Alzheimer disease (FAD)G D Schellenberg, H Payami, E M Wijsman, et al.
Clinical Oncology (Royal College of Radiologists (Great Britain))|February 23, 2019
Stereotactic Body Radiotherapy for Small Unresectable Hepatocellular CarcinomasR Yeung, L Beaton, T Rackley, et al.
American Journal of Human Genetics|February 1, 1997
Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative GroupC E Yu, J Oshima, E M Wijsman, et al.
Pageof 51