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J I Rotter

Showing results (171-180 of 214) with videos related to

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American Journal of Human Genetics|July 27, 1999
A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11B E Aouizerat, H Allayee, R M Cantor, et al.
Human Molecular Genetics|August 25, 2000
Identification of TNFRSF1B as a novel modifier gene in familial combined hyperlipidemiaJ M Geurts, R G Janssen, M M van Greevenbroek, et al.
Hypertension (Dallas, Tex. : 1979)|October 20, 2001
Genome scan for blood pressure in Dutch dyslipidemic families reveals linkage to a locus on chromosome 4pH Allayee, T W de Bruin, K Michelle Dominguez, et al.
Gut|October 4, 2008
Linkage of Crohn's disease-related serological phenotypes: NFKB1 haplotypes are associated with anti-CBir1 and ASCA, and show reduced NF-kappaB activationH Takedatsu, K D Taylor, L Mei, et al.
The Journal of Clinical Investigation|April 20, 1999
PARP alleles within the linked chromosomal region are associated with systemic lupus erythematosusB P Tsao, R M Cantor, J M Grossman, et al.
Circulation|January 4, 2001
Evidence for joint genetic control of insulin sensitivity and systolic blood pressure in hispanic families with a hypertensive probandA H Xiang, S P Azen, L J Raffel, et al.
Human Molecular Genetics|October 1, 1996
Susceptibility locus for inflammatory bowel disease on chromosome 16 has a role in Crohn's disease, but not in ulcerative colitisJ D Ohmen, H Y Yang, K K Yamamoto, et al.
Diabetologia|March 16, 2013
Systematic evaluation of validated type 2 diabetes and glycaemic trait loci for association with insulin clearanceM O Goodarzi, X Guo, J Cui, et al.
Clinical Genetics|October 9, 2012
The M694V mutation in Armenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLAF S Ong, H Vakil, Y Xue, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosisM Shohat, N Magal, T Shohat, et al.
Pageof 22

Showing results (171-180 of 214) with videos related to

Sort By:
Pageof 22
American Journal of Human Genetics|July 27, 1999
A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11B E Aouizerat, H Allayee, R M Cantor, et al.
Human Molecular Genetics|August 25, 2000
Identification of TNFRSF1B as a novel modifier gene in familial combined hyperlipidemiaJ M Geurts, R G Janssen, M M van Greevenbroek, et al.
Hypertension (Dallas, Tex. : 1979)|October 20, 2001
Genome scan for blood pressure in Dutch dyslipidemic families reveals linkage to a locus on chromosome 4pH Allayee, T W de Bruin, K Michelle Dominguez, et al.
Gut|October 4, 2008
Linkage of Crohn's disease-related serological phenotypes: NFKB1 haplotypes are associated with anti-CBir1 and ASCA, and show reduced NF-kappaB activationH Takedatsu, K D Taylor, L Mei, et al.
The Journal of Clinical Investigation|April 20, 1999
PARP alleles within the linked chromosomal region are associated with systemic lupus erythematosusB P Tsao, R M Cantor, J M Grossman, et al.
Circulation|January 4, 2001
Evidence for joint genetic control of insulin sensitivity and systolic blood pressure in hispanic families with a hypertensive probandA H Xiang, S P Azen, L J Raffel, et al.
Human Molecular Genetics|October 1, 1996
Susceptibility locus for inflammatory bowel disease on chromosome 16 has a role in Crohn's disease, but not in ulcerative colitisJ D Ohmen, H Y Yang, K K Yamamoto, et al.
Diabetologia|March 16, 2013
Systematic evaluation of validated type 2 diabetes and glycaemic trait loci for association with insulin clearanceM O Goodarzi, X Guo, J Cui, et al.
Clinical Genetics|October 9, 2012
The M694V mutation in Armenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLAF S Ong, H Vakil, Y Xue, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosisM Shohat, N Magal, T Shohat, et al.
Pageof 22