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

S Sparkes

Showing results (261-270 of 276) with videos related to

Pageof 28
Sort By:
The Journal of Biological Chemistry|December 5, 1986
Regulation of rat liver 3-hydroxy-3-methylglutaryl coenzyme A synthase and the chromosomal localization of the human geneM Mehrabian, K A Callaway, C F Clarke, et al.
Biochimica Et Biophysica Acta|April 6, 1990
Induction of a human carbonyl reductase gene located on chromosome 21G L Forrest, S Akman, S Krutzik, et al.
Somatic Cell and Molecular Genetics|September 1, 1984
Wilms' tumor-aniridia association: segregation of affected chromosome in somatic cell hybrids, identification of cell surface antigen associated with deleted area, and regional mapping of c-Ha-ras-1 oncogene, insulin gene, and beta-globin geneJ H Fisher, Y E Miller, R S Sparkes, et al.
Journal of Medical Genetics|August 1, 1982
Linkage analysis of five pedigrees affected with typical autosomal dominant retinitis pigmentosaL L Field, J R Heckenlively, R S Sparkes, et al.
Genomics|September 15, 1994
Assignment of the zeta-crystallin gene (CRYZ) to human chromosome 1p22-p31 and identification of restriction fragment length polymorphismsC Heinzmann, T L Kojis, P Gonzalez, et al.
American Journal of Ophthalmology|March 28, 2006
Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataractDavid D Geyer, M Anne Spence, Meriam Johannes, et al.
Transactions of the American Ophthalmological Society|January 1, 1993
Linkage analysis of Norrie disease with an X-chromosomal ornithine aminotransferase locusJ B Bateman, T L Kojis, R M Cantor, et al.
Diabetologia|October 1, 1983
Association studies between Type 1 (insulin-dependent) diabetes and 27 genetic markers: lack of association between Type 1 diabetes and Kidd blood groupS E Hodge, C E Anderson, K Neiswanger, et al.
Diabetes|July 1, 1992
Genetic marker associations with proliferative retinopathy in persons diagnosed with diabetes before 30 yr of ageK J Cruickshanks, C M Vadheim, S E Moss, et al.
Genomics|November 1, 1993
Linkage mapping of 40 randomly isolated liver cDNA clones in the mouseC H Warden, M Mehrabian, K Y He, et al.
Pageof 28

Showing results (261-270 of 276) with videos related to

Sort By:
Pageof 28
The Journal of Biological Chemistry|December 5, 1986
Regulation of rat liver 3-hydroxy-3-methylglutaryl coenzyme A synthase and the chromosomal localization of the human geneM Mehrabian, K A Callaway, C F Clarke, et al.
Biochimica Et Biophysica Acta|April 6, 1990
Induction of a human carbonyl reductase gene located on chromosome 21G L Forrest, S Akman, S Krutzik, et al.
Somatic Cell and Molecular Genetics|September 1, 1984
Wilms' tumor-aniridia association: segregation of affected chromosome in somatic cell hybrids, identification of cell surface antigen associated with deleted area, and regional mapping of c-Ha-ras-1 oncogene, insulin gene, and beta-globin geneJ H Fisher, Y E Miller, R S Sparkes, et al.
Journal of Medical Genetics|August 1, 1982
Linkage analysis of five pedigrees affected with typical autosomal dominant retinitis pigmentosaL L Field, J R Heckenlively, R S Sparkes, et al.
Genomics|September 15, 1994
Assignment of the zeta-crystallin gene (CRYZ) to human chromosome 1p22-p31 and identification of restriction fragment length polymorphismsC Heinzmann, T L Kojis, P Gonzalez, et al.
American Journal of Ophthalmology|March 28, 2006
Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataractDavid D Geyer, M Anne Spence, Meriam Johannes, et al.
Transactions of the American Ophthalmological Society|January 1, 1993
Linkage analysis of Norrie disease with an X-chromosomal ornithine aminotransferase locusJ B Bateman, T L Kojis, R M Cantor, et al.
Diabetologia|October 1, 1983
Association studies between Type 1 (insulin-dependent) diabetes and 27 genetic markers: lack of association between Type 1 diabetes and Kidd blood groupS E Hodge, C E Anderson, K Neiswanger, et al.
Diabetes|July 1, 1992
Genetic marker associations with proliferative retinopathy in persons diagnosed with diabetes before 30 yr of ageK J Cruickshanks, C M Vadheim, S E Moss, et al.
Genomics|November 1, 1993
Linkage mapping of 40 randomly isolated liver cDNA clones in the mouseC H Warden, M Mehrabian, K Y He, et al.
Pageof 28