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Jonathan C Cohen

Showing results (51-60 of 117) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|April 9, 2009
Genetic and metabolic determinants of plasma PCSK9 levelsSusan G Lakoski, Thomas A Lagace, Jonathan C Cohen, et al.
The Journal of Biological Chemistry|March 10, 2009
Genetic variation in ANGPTL4 provides insights into protein processing and functionWu Yin, Stefano Romeo, Shurong Chang, et al.
The Journal of Biological Chemistry|December 15, 2005
Functional asymmetry of nucleotide-binding domains in ABCG5 and ABCG8Da-Wei Zhang, Gregory A Graf, Robert D Gerard, et al.
Journal of Lipid Research|November 8, 2014
Relative roles of ABCG5/ABCG8 in liver and intestineJin Wang, Matthew A Mitsche, Dieter Lütjohann, et al.
The Journal of Biological Chemistry|May 15, 2003
Normal sorting but defective endocytosis of the low density lipoprotein receptor in mice with autosomal recessive hypercholesterolemiaChristopher Jones, Robert E Hammer, Wei-Ping Li, et al.
Nature Genetics|April 25, 2017
Adiposity amplifies the genetic risk of fatty liver disease conferred by multiple lociStefan Stender, Julia Kozlitina, Børge G Nordestgaard, et al.
Science (New York, N.Y.)|August 7, 2004
Multiple rare alleles contribute to low plasma levels of HDL cholesterolJonathan C Cohen, Robert S Kiss, Alexander Pertsemlidis, et al.
Journal of Lipid Research|June 3, 2005
ABCG5 and ABCG8 require MDR2 for secretion of cholesterol into bileSilvia Langheim, Liqing Yu, Klaus von Bergmann, et al.
The Journal of Clinical Investigation|December 17, 2008
Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humansStefano Romeo, Wu Yin, Julia Kozlitina, et al.
Human Molecular Genetics|November 6, 2002
Two independent apolipoprotein A5 haplotypes influence human plasma triglyceride levelsLen A Pennacchio, Michael Olivier, Jaroslav A Hubacek, et al.
Pageof 12

Showing results (51-60 of 117) with videos related to

Sort By:
Pageof 12
The Journal of Clinical Endocrinology and Metabolism|April 9, 2009
Genetic and metabolic determinants of plasma PCSK9 levelsSusan G Lakoski, Thomas A Lagace, Jonathan C Cohen, et al.
The Journal of Biological Chemistry|March 10, 2009
Genetic variation in ANGPTL4 provides insights into protein processing and functionWu Yin, Stefano Romeo, Shurong Chang, et al.
The Journal of Biological Chemistry|December 15, 2005
Functional asymmetry of nucleotide-binding domains in ABCG5 and ABCG8Da-Wei Zhang, Gregory A Graf, Robert D Gerard, et al.
Journal of Lipid Research|November 8, 2014
Relative roles of ABCG5/ABCG8 in liver and intestineJin Wang, Matthew A Mitsche, Dieter Lütjohann, et al.
The Journal of Biological Chemistry|May 15, 2003
Normal sorting but defective endocytosis of the low density lipoprotein receptor in mice with autosomal recessive hypercholesterolemiaChristopher Jones, Robert E Hammer, Wei-Ping Li, et al.
Nature Genetics|April 25, 2017
Adiposity amplifies the genetic risk of fatty liver disease conferred by multiple lociStefan Stender, Julia Kozlitina, Børge G Nordestgaard, et al.
Science (New York, N.Y.)|August 7, 2004
Multiple rare alleles contribute to low plasma levels of HDL cholesterolJonathan C Cohen, Robert S Kiss, Alexander Pertsemlidis, et al.
Journal of Lipid Research|June 3, 2005
ABCG5 and ABCG8 require MDR2 for secretion of cholesterol into bileSilvia Langheim, Liqing Yu, Klaus von Bergmann, et al.
The Journal of Clinical Investigation|December 17, 2008
Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humansStefano Romeo, Wu Yin, Julia Kozlitina, et al.
Human Molecular Genetics|November 6, 2002
Two independent apolipoprotein A5 haplotypes influence human plasma triglyceride levelsLen A Pennacchio, Michael Olivier, Jaroslav A Hubacek, et al.
Pageof 12