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Nucleic Acids Research
|
August 17, 2018
INFERNO: inferring the molecular mechanisms of noncoding genetic variants
Alexandre 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 study
W 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 association
Chang-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 mutation
Katsutoshi 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 phenotype
James 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 14
G 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 Tanzania
C 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 Carcinomas
R 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 Group
C E Yu, J Oshima, E M Wijsman, et al.
Page
of 51
Search research articles
Search
Showing results (181-190 of 503) with videos related to
Sort By:
Page
of 51
Nucleic Acids Research
|
August 17, 2018
INFERNO: inferring the molecular mechanisms of noncoding genetic variants
Alexandre 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 study
W 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 association
Chang-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 mutation
Katsutoshi 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 phenotype
James 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 14
G 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 Tanzania
C 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 Carcinomas
R 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 Group
C E Yu, J Oshima, E M Wijsman, et al.
Page
of 51