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J I Rotter

Showing results (131-140 of 214) with videos related to

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Progress in Clinical and Biological Research|January 1, 1982
Workshop on genetics of diabetesJ I Rotter, P Platz, C E Anderson, et al.
The New England Journal of Medicine|January 11, 1979
Duodenal-ulcer disease associated with elevated serum pepsinogen I: an inherited autosomal dominant disorderJ I Rotter, J Q Sones, I M Samloff, et al.
Nature|November 14, 1991
Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibilityC Julier, R N Hyer, J Davies, et al.
Journal of Lipid Research|January 1, 1996
Apolipoprotein A-I/C-III/A-IV gene cluster in familial combined hyperlipidemia: effects on LDL-cholesterol and apolipoproteins B and C-IIIG M Dallinga-Thie, X D Bu, M van Linde-Sibenius Trip, et al.
The Pharmacogenomics Journal|May 21, 2016
Statin-induced expression change of INSIG1 in lymphoblastoid cell lines correlates with plasma triglyceride statin response in a sex-specific mannerE Theusch, K Kim, K Stevens, et al.
Diabetes|May 1, 1996
Association of HLA-DPB1*0301 with IDDM in Mexican-AmericansH A Erlich, J I Rotter, J D Chang, et al.
The Pharmacogenomics Journal|March 2, 2016
Statin-induced expression change of INSIG1 in lymphoblastoid cell lines correlates with plasma triglyceride statin response in a sex-specific mannerE Theusch, K Kim, K Stevens, et al.
Current Opinion in Lipidology|May 18, 1999
Novel genes for familial combined hyperlipidemiaB E Aouizerat, H Allayee, J Bodnar, et al.
Genomics|September 1, 1990
Serum amyloid A and P protein genes in familial Mediterranean feverM Shohat, T Shohat, J I Rotter, et al.
American Journal of Human Genetics|May 2, 2000
Candidate locus for a nuclear modifier gene for maternally inherited deafnessY Bykhovskaya, X Estivill, K Taylor, et al.
Pageof 22

Showing results (131-140 of 214) with videos related to

Sort By:
Pageof 22
Progress in Clinical and Biological Research|January 1, 1982
Workshop on genetics of diabetesJ I Rotter, P Platz, C E Anderson, et al.
The New England Journal of Medicine|January 11, 1979
Duodenal-ulcer disease associated with elevated serum pepsinogen I: an inherited autosomal dominant disorderJ I Rotter, J Q Sones, I M Samloff, et al.
Nature|November 14, 1991
Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibilityC Julier, R N Hyer, J Davies, et al.
Journal of Lipid Research|January 1, 1996
Apolipoprotein A-I/C-III/A-IV gene cluster in familial combined hyperlipidemia: effects on LDL-cholesterol and apolipoproteins B and C-IIIG M Dallinga-Thie, X D Bu, M van Linde-Sibenius Trip, et al.
The Pharmacogenomics Journal|May 21, 2016
Statin-induced expression change of INSIG1 in lymphoblastoid cell lines correlates with plasma triglyceride statin response in a sex-specific mannerE Theusch, K Kim, K Stevens, et al.
Diabetes|May 1, 1996
Association of HLA-DPB1*0301 with IDDM in Mexican-AmericansH A Erlich, J I Rotter, J D Chang, et al.
The Pharmacogenomics Journal|March 2, 2016
Statin-induced expression change of INSIG1 in lymphoblastoid cell lines correlates with plasma triglyceride statin response in a sex-specific mannerE Theusch, K Kim, K Stevens, et al.
Current Opinion in Lipidology|May 18, 1999
Novel genes for familial combined hyperlipidemiaB E Aouizerat, H Allayee, J Bodnar, et al.
Genomics|September 1, 1990
Serum amyloid A and P protein genes in familial Mediterranean feverM Shohat, T Shohat, J I Rotter, et al.
American Journal of Human Genetics|May 2, 2000
Candidate locus for a nuclear modifier gene for maternally inherited deafnessY Bykhovskaya, X Estivill, K Taylor, et al.
Pageof 22