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Matthew R Ban

Showing results (31-40 of 40) with videos related to

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Cardiovascular Diabetology|March 15, 2008
Association between the FTO rs9939609 polymorphism and the metabolic syndrome in a non-Caucasian multi-ethnic sampleSalam A Al-Attar, Rebecca L Pollex, Matthew R Ban, et al.
Journal of Lipid Research|September 6, 2017
Polygenic determinants in extremes of high-density lipoprotein cholesterolJacqueline S Dron, Jian Wang, Cécile Low-Kam, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 22, 2016
Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained ClinicallyJian Wang, Jacqueline S Dron, Matthew R Ban, et al.
Circulation. Cardiovascular Genetics|November 22, 2014
Common low-density lipoprotein receptor p.G116S variant has a large effect on plasma low-density lipoprotein cholesterol in circumpolar inuit populationsJoseph B Dubé, Jian Wang, Henian Cao, et al.
Circulation. Cardiovascular Genetics|December 3, 2011
Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemiaChristopher T Johansen, Jian Wang, Adam D McIntyre, et al.
Atherosclerosis|May 17, 2016
Targeted exonic sequencing of GWAS loci in the high extremes of the plasma lipids distributionAniruddh P Patel, Gina M Peloso, James P Pirruccello, et al.
The Canadian Journal of Cardiology|April 30, 2013
Western Database of Lipid Variants (WDLV): a catalogue of genetic variants in monogenic dyslipidemiasJennifer Fu, Samantha Kwok, Leah Sinai, et al.
Nature Genetics|July 27, 2010
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 21, 2011
An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
American Journal of Human Genetics|December 14, 2011
TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zoneLijia Huang, Katarzyna Szymanska, Victor L Jensen, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Cardiovascular Diabetology|March 15, 2008
Association between the FTO rs9939609 polymorphism and the metabolic syndrome in a non-Caucasian multi-ethnic sampleSalam A Al-Attar, Rebecca L Pollex, Matthew R Ban, et al.
Journal of Lipid Research|September 6, 2017
Polygenic determinants in extremes of high-density lipoprotein cholesterolJacqueline S Dron, Jian Wang, Cécile Low-Kam, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 22, 2016
Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained ClinicallyJian Wang, Jacqueline S Dron, Matthew R Ban, et al.
Circulation. Cardiovascular Genetics|November 22, 2014
Common low-density lipoprotein receptor p.G116S variant has a large effect on plasma low-density lipoprotein cholesterol in circumpolar inuit populationsJoseph B Dubé, Jian Wang, Henian Cao, et al.
Circulation. Cardiovascular Genetics|December 3, 2011
Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemiaChristopher T Johansen, Jian Wang, Adam D McIntyre, et al.
Atherosclerosis|May 17, 2016
Targeted exonic sequencing of GWAS loci in the high extremes of the plasma lipids distributionAniruddh P Patel, Gina M Peloso, James P Pirruccello, et al.
The Canadian Journal of Cardiology|April 30, 2013
Western Database of Lipid Variants (WDLV): a catalogue of genetic variants in monogenic dyslipidemiasJennifer Fu, Samantha Kwok, Leah Sinai, et al.
Nature Genetics|July 27, 2010
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 21, 2011
An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
American Journal of Human Genetics|December 14, 2011
TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zoneLijia Huang, Katarzyna Szymanska, Victor L Jensen, et al.
Pageof 4