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Journal of Molecular Biology
|
April 25, 1974
Kinetic studies of gene frequency. I. Use of a DNA copy of reticulocyte 9 S RNA to estimate globin gene dosage in mouse tissues
P R Harrison, G D Birnie, A Hell, et al.
Clinical Genetics
|
July 1, 1991
Identification of the 664 proline to leucine mutation in the low density lipoprotein receptor in four unrelated patients with familial hypercholesterolaemia in the UK
L King-Underwood, V Gudnason, S Humphries, et al.
Arteriosclerosis (Dallas, Tex.)
|
July 1, 1990
Familial defective apolipoprotein B-100. Comparison with familial hypercholesterolemia in 18 cases detected in Munich
H Schuster, G Rauh, B Kormann, et al.
The Journal of Clinical Investigation
|
November 1, 1988
Genetic evidence from two families that the apolipoprotein B gene is not involved in abetalipoproteinemia
P J Talmud, J K Lloyd, D P Muller, et al.
Arteriosclerosis (Dallas, Tex.)
|
January 1, 1989
Gene probes in diagnosis of familial hypercholesterolemia
S Humphries, R Taylor, M Jeenah, et al.
Journal of Medical Genetics
|
April 1, 1993
Six DNA polymorphisms in the low density lipoprotein receptor gene: their genetic relationship and an example of their use for identifying affected relatives of patients with familial hypercholesterolaemia
S Humphries, L King-Underwood, V Gudnason, et al.
The Science of the Total Environment
|
December 14, 2024
Waterborne contaminants in high intensity agriculture and plant production: A review of on-site and downstream impacts
Megan Gomes, Timothy J Ralph, Marc S Humphries, et al.
European Journal of Clinical Investigation
|
March 27, 1999
Cholesteryl ester transfer protein gene effect on CETP activity and plasma high-density lipoprotein in European populations. The EARS Group
V Gudnason, S Kakko, V Nicaud, et al.
Human Genetics
|
May 17, 2001
Elite swimmers and the D allele of the ACE I/D polymorphism
D Woods, M Hickman, Y Jamshidi, et al.
Atherosclerosis
|
August 1, 1991
Rapid screening for specific mutations in patients with a clinical diagnosis of familial hypercholesterolaemia
P Talmud, A Tybjaerg-Hansen, D Bhatnagar, et al.
Page
of 28
Search research articles
Search
Showing results (141-150 of 279) with videos related to
Sort By:
Page
of 28
Journal of Molecular Biology
|
April 25, 1974
Kinetic studies of gene frequency. I. Use of a DNA copy of reticulocyte 9 S RNA to estimate globin gene dosage in mouse tissues
P R Harrison, G D Birnie, A Hell, et al.
Clinical Genetics
|
July 1, 1991
Identification of the 664 proline to leucine mutation in the low density lipoprotein receptor in four unrelated patients with familial hypercholesterolaemia in the UK
L King-Underwood, V Gudnason, S Humphries, et al.
Arteriosclerosis (Dallas, Tex.)
|
July 1, 1990
Familial defective apolipoprotein B-100. Comparison with familial hypercholesterolemia in 18 cases detected in Munich
H Schuster, G Rauh, B Kormann, et al.
The Journal of Clinical Investigation
|
November 1, 1988
Genetic evidence from two families that the apolipoprotein B gene is not involved in abetalipoproteinemia
P J Talmud, J K Lloyd, D P Muller, et al.
Arteriosclerosis (Dallas, Tex.)
|
January 1, 1989
Gene probes in diagnosis of familial hypercholesterolemia
S Humphries, R Taylor, M Jeenah, et al.
Journal of Medical Genetics
|
April 1, 1993
Six DNA polymorphisms in the low density lipoprotein receptor gene: their genetic relationship and an example of their use for identifying affected relatives of patients with familial hypercholesterolaemia
S Humphries, L King-Underwood, V Gudnason, et al.
The Science of the Total Environment
|
December 14, 2024
Waterborne contaminants in high intensity agriculture and plant production: A review of on-site and downstream impacts
Megan Gomes, Timothy J Ralph, Marc S Humphries, et al.
European Journal of Clinical Investigation
|
March 27, 1999
Cholesteryl ester transfer protein gene effect on CETP activity and plasma high-density lipoprotein in European populations. The EARS Group
V Gudnason, S Kakko, V Nicaud, et al.
Human Genetics
|
May 17, 2001
Elite swimmers and the D allele of the ACE I/D polymorphism
D Woods, M Hickman, Y Jamshidi, et al.
Atherosclerosis
|
August 1, 1991
Rapid screening for specific mutations in patients with a clinical diagnosis of familial hypercholesterolaemia
P Talmud, A Tybjaerg-Hansen, D Bhatnagar, et al.
Page
of 28