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

Anne P Beigneux

Showing results (11-20 of 82) with videos related to

Pageof 9
Sort By:
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 6, 2018
An ELISA for quantifying GPIHBP1 autoantibodies and making a diagnosis of the GPIHBP1 autoantibody syndromeKazuya Miyashita, Isamu Fukamachi, Tetsuo Machida, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 29, 2022
A protein of capillary endothelial cells, GPIHBP1, is crucial for plasma triglyceride metabolismStephen G Young, Wenxin Song, Ye Yang, et al.
The Journal of Clinical Investigation|February 18, 2004
Inactivation of Icmt inhibits transformation by oncogenic K-Ras and B-RafMartin O Bergo, Bryant J Gavino, Christine Hong, et al.
Journal of Lipid Research|July 12, 2017
Apolipoprotein C-III inhibits triglyceride hydrolysis by GPIHBP1-bound LPLMikael Larsson, Christopher M Allan, Rachel S Jung, et al.
The Journal of Biological Chemistry|September 4, 2009
Highly conserved cysteines within the Ly6 domain of GPIHBP1 are crucial for the binding of lipoprotein lipaseAnne P Beigneux, Peter Gin, Brandon S J Davies, et al.
Current Opinion in Lipidology|July 11, 2007
GPIHBP1: an endothelial cell molecule important for the lipolytic processing of chylomicronsStephen G Young, Brandon S J Davies, Loren G Fong, et al.
Current Opinion in Lipidology|April 17, 2009
GPIHBP1 and lipolysis: an updateAnne P Beigneux, Michael M Weinstein, Brandon S J Davies, et al.
Biochimica Et Biophysica Acta|November 13, 2007
Normal binding of lipoprotein lipase, chylomicrons, and apo-AV to GPIHBP1 containing a G56R amino acid substitutionPeter Gin, Anne P Beigneux, Brandon Davies, et al.
Circulation Research|November 13, 2014
GPIHBP1 missense mutations often cause multimerization of GPIHBP1 and thereby prevent lipoprotein lipase bindingAnne P Beigneux, Loren G Fong, André Bensadoun, et al.
Journal of Lipid Research|November 5, 2016
Mobility of "HSPG-bound" LPL explains how LPL is able to reach GPIHBP1 on capillariesChristopher M Allan, Mikael Larsson, Rachel S Jung, et al.
Pageof 9

Showing results (11-20 of 82) with videos related to

Sort By:
Pageof 9
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 6, 2018
An ELISA for quantifying GPIHBP1 autoantibodies and making a diagnosis of the GPIHBP1 autoantibody syndromeKazuya Miyashita, Isamu Fukamachi, Tetsuo Machida, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 29, 2022
A protein of capillary endothelial cells, GPIHBP1, is crucial for plasma triglyceride metabolismStephen G Young, Wenxin Song, Ye Yang, et al.
The Journal of Clinical Investigation|February 18, 2004
Inactivation of Icmt inhibits transformation by oncogenic K-Ras and B-RafMartin O Bergo, Bryant J Gavino, Christine Hong, et al.
Journal of Lipid Research|July 12, 2017
Apolipoprotein C-III inhibits triglyceride hydrolysis by GPIHBP1-bound LPLMikael Larsson, Christopher M Allan, Rachel S Jung, et al.
The Journal of Biological Chemistry|September 4, 2009
Highly conserved cysteines within the Ly6 domain of GPIHBP1 are crucial for the binding of lipoprotein lipaseAnne P Beigneux, Peter Gin, Brandon S J Davies, et al.
Current Opinion in Lipidology|July 11, 2007
GPIHBP1: an endothelial cell molecule important for the lipolytic processing of chylomicronsStephen G Young, Brandon S J Davies, Loren G Fong, et al.
Current Opinion in Lipidology|April 17, 2009
GPIHBP1 and lipolysis: an updateAnne P Beigneux, Michael M Weinstein, Brandon S J Davies, et al.
Biochimica Et Biophysica Acta|November 13, 2007
Normal binding of lipoprotein lipase, chylomicrons, and apo-AV to GPIHBP1 containing a G56R amino acid substitutionPeter Gin, Anne P Beigneux, Brandon Davies, et al.
Circulation Research|November 13, 2014
GPIHBP1 missense mutations often cause multimerization of GPIHBP1 and thereby prevent lipoprotein lipase bindingAnne P Beigneux, Loren G Fong, André Bensadoun, et al.
Journal of Lipid Research|November 5, 2016
Mobility of "HSPG-bound" LPL explains how LPL is able to reach GPIHBP1 on capillariesChristopher M Allan, Mikael Larsson, Rachel S Jung, et al.
Pageof 9