Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

N D Carter

Showing results (121-130 of 140) with videos related to

Pageof 14
Sort By:
Lancet (London, England)|September 24, 1977
Vitamin-D metabolism in nephrotic syndromeJ M Barragry, M W France, N D Carter, et al.
Journal of Hypertension|August 1, 1994
Angiotensin converting enzyme insertion/deletion polymorphism: association with ethnic originJ Barley, A Blackwood, N D Carter, et al.
Clinical Science (London, England : 1979)|September 9, 1998
Methylenetetrahydrofolate reductase polymorphism (C-677T) and coronary artery diseaseN M Malik, P Syrris, R Schwartzman, et al.
The Journal of Clinical Investigation|January 1, 1979
A study of human leukocyte D locus related antigens in Graves' diseaseN R Farid, L Sampson, E P Noel, et al.
Journal of Medical Genetics|June 28, 2006
AMP-kinase alpha2 subunit gene PRKAA2 variants are associated with total cholesterol, low-density lipoprotein-cholesterol and high-density lipoprotein-cholesterol in normal womenN J Spencer-Jones, D Ge, H Snieder, et al.
Human Molecular Genetics|January 15, 1999
Genetic control of the circulating concentration of transforming growth factor type beta1D J Grainger, K Heathcote, M Chiano, et al.
Journal of Medical Genetics|September 9, 2000
Cytosine methylation confers instability on the cardiac troponin T gene in hypertrophic cardiomyopathyL G D'Cruz, C Baboonian, H E Phillimore, et al.
Human Heredity|January 1, 1976
A study of several genetic biochemical markers in Sherpas with description of some variant phenotypesA S Santachiara-Benerecetti, E W Baur, M Beretta, et al.
Journal of Human Hypertension|January 1, 1996
Angiotensin converting enzyme gene I/D polymorphism, blood pressure and the renin-angiotensin system in Caucasian and Afro-Caribbean peoplesJ Barley, A Blackwood, M Miller, et al.
The British Journal of Dermatology|June 3, 1999
Lack of c-kit mutation in familial urticaria pigmentosaJ L Rosbotham, N M Malik, P Syrris, et al.
Pageof 14

Showing results (121-130 of 140) with videos related to

Sort By:
Pageof 14
Lancet (London, England)|September 24, 1977
Vitamin-D metabolism in nephrotic syndromeJ M Barragry, M W France, N D Carter, et al.
Journal of Hypertension|August 1, 1994
Angiotensin converting enzyme insertion/deletion polymorphism: association with ethnic originJ Barley, A Blackwood, N D Carter, et al.
Clinical Science (London, England : 1979)|September 9, 1998
Methylenetetrahydrofolate reductase polymorphism (C-677T) and coronary artery diseaseN M Malik, P Syrris, R Schwartzman, et al.
The Journal of Clinical Investigation|January 1, 1979
A study of human leukocyte D locus related antigens in Graves' diseaseN R Farid, L Sampson, E P Noel, et al.
Journal of Medical Genetics|June 28, 2006
AMP-kinase alpha2 subunit gene PRKAA2 variants are associated with total cholesterol, low-density lipoprotein-cholesterol and high-density lipoprotein-cholesterol in normal womenN J Spencer-Jones, D Ge, H Snieder, et al.
Human Molecular Genetics|January 15, 1999
Genetic control of the circulating concentration of transforming growth factor type beta1D J Grainger, K Heathcote, M Chiano, et al.
Journal of Medical Genetics|September 9, 2000
Cytosine methylation confers instability on the cardiac troponin T gene in hypertrophic cardiomyopathyL G D'Cruz, C Baboonian, H E Phillimore, et al.
Human Heredity|January 1, 1976
A study of several genetic biochemical markers in Sherpas with description of some variant phenotypesA S Santachiara-Benerecetti, E W Baur, M Beretta, et al.
Journal of Human Hypertension|January 1, 1996
Angiotensin converting enzyme gene I/D polymorphism, blood pressure and the renin-angiotensin system in Caucasian and Afro-Caribbean peoplesJ Barley, A Blackwood, M Miller, et al.
The British Journal of Dermatology|June 3, 1999
Lack of c-kit mutation in familial urticaria pigmentosaJ L Rosbotham, N M Malik, P Syrris, et al.
Pageof 14