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R E Ferrell

Showing results (161-170 of 371) with videos related to

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Arteriosclerosis, Thrombosis, and Vascular Biology|February 12, 1999
The relationship between risk factor levels and presence of coronary artery calcification is dependent on apolipoprotein E genotypeS L Kardia, M B Haviland, R E Ferrell, et al.
Biochemical Genetics|December 1, 1973
Characterization of a new variant of human red cell carbonic anhydrase I, CA If London (Glu-102 leads to Lys)N D Carter, R J Tanis, R E Tashian, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|May 1, 1994
A common deletion polymorphism in the apolipoprotein A4 gene and its significance in lipid metabolismM I Kamboh, J S Friedlaender, Y I Ahn, et al.
American Journal of Hypertension|January 5, 2002
Role of angiotensin converting enzyme genotype in sodium sensitivity in older hypertensivesD R Dengel, M D Brown, R E Ferrell, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 9, 2001
A common promotor variant in the cytochrome P450c17alpha (CYP17) gene is associated with bioavailability testosterone levels and bone size in menJ M Zmuda, J A Cauley, L H Kuller, et al.
Genome Research|March 7, 2001
A combinatorial partitioning method to identify multilocus genotypic partitions that predict quantitative trait variationM R Nelson, S L Kardia, R E Ferrell, et al.
American Journal of Medical Genetics|March 1, 1984
A syndrome of microcephaly and retinal pigmentary abnormalities without mental retardation in a family with coincidental autosomal dominant hyperreflexiaJ T Parke, V M Riccardi, R A Lewis, et al.
Nature Genetics|August 1, 1995
APOE*4-associated Alzheimer's disease risk is modified by alpha 1-antichymotrypsin polymorphismM I Kamboh, D K Sanghera, R E Ferrell, et al.
Clinical Genetics|September 1, 1996
X-linked exudative vitreoretinopathy caused by an arginine to leucine substitution (R121L) in the Norrie disease proteinK Johnson, H A Mintz-Hittner, Y P Conley, et al.
American Journal of Human Genetics|July 1, 1989
Genetic studies of human apolipoproteins. IX. Apolipoprotein D polymorphism and its relation to serum lipoprotein lipid levelsM I Kamboh, J J Albers, P P Majumder, et al.
Pageof 38

Showing results (161-170 of 371) with videos related to

Sort By:
Pageof 38
Arteriosclerosis, Thrombosis, and Vascular Biology|February 12, 1999
The relationship between risk factor levels and presence of coronary artery calcification is dependent on apolipoprotein E genotypeS L Kardia, M B Haviland, R E Ferrell, et al.
Biochemical Genetics|December 1, 1973
Characterization of a new variant of human red cell carbonic anhydrase I, CA If London (Glu-102 leads to Lys)N D Carter, R J Tanis, R E Tashian, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|May 1, 1994
A common deletion polymorphism in the apolipoprotein A4 gene and its significance in lipid metabolismM I Kamboh, J S Friedlaender, Y I Ahn, et al.
American Journal of Hypertension|January 5, 2002
Role of angiotensin converting enzyme genotype in sodium sensitivity in older hypertensivesD R Dengel, M D Brown, R E Ferrell, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 9, 2001
A common promotor variant in the cytochrome P450c17alpha (CYP17) gene is associated with bioavailability testosterone levels and bone size in menJ M Zmuda, J A Cauley, L H Kuller, et al.
Genome Research|March 7, 2001
A combinatorial partitioning method to identify multilocus genotypic partitions that predict quantitative trait variationM R Nelson, S L Kardia, R E Ferrell, et al.
American Journal of Medical Genetics|March 1, 1984
A syndrome of microcephaly and retinal pigmentary abnormalities without mental retardation in a family with coincidental autosomal dominant hyperreflexiaJ T Parke, V M Riccardi, R A Lewis, et al.
Nature Genetics|August 1, 1995
APOE*4-associated Alzheimer's disease risk is modified by alpha 1-antichymotrypsin polymorphismM I Kamboh, D K Sanghera, R E Ferrell, et al.
Clinical Genetics|September 1, 1996
X-linked exudative vitreoretinopathy caused by an arginine to leucine substitution (R121L) in the Norrie disease proteinK Johnson, H A Mintz-Hittner, Y P Conley, et al.
American Journal of Human Genetics|July 1, 1989
Genetic studies of human apolipoproteins. IX. Apolipoprotein D polymorphism and its relation to serum lipoprotein lipid levelsM I Kamboh, J J Albers, P P Majumder, et al.
Pageof 38