Citations for
1GPIHBP1, LMF1, LPL
Structure of lipoprotein lipase in complex with GPIHBP1.
Arora R, Nimonkar AV, Baird D, Wang C, Chiu CH, Horton PA, Hanrahan S, Cubbon R, Weldon S, Tschantz WR, Mueller S, Brunner R, Lehr P, Meier P, Ottl J, Voznesensky A, Pandey P, Smith TM, Stojanovic A, Flyer A, Benson TE, Romanowski MJ, Trauger JW.
Proc Natl Acad Sci U S A 116(21):10360-10365. doi: 10.1073/pnas.1820171116. Epub 2019 May 9. 2019
2GPIHBP1, LPL
Structure of the lipoprotein lipase-GPIHBP1 complex that mediates plasma triglyceride hydrolysis.
Birrane G, Beigneux AP, Dwyer B, Strack-Logue B, Kristensen KK, Francone OL, Fong LG, Mertens HDT, Pan CQ, Ploug M, Young SG, Meiyappan M.
Proc Natl Acad Sci U S A. Jan 29;116(5):1723-1732. doi: 10.1073/pnas.1817984116. Epub 2018 Dec 17. 2019
3ANGPTL4, GPIHBP1, LPL
Angiopoietin-like 4 Modifies the Interactions between Lipoprotein Lipase and Its Endothelial Cell Transporter GPIHBP1.
Chi X, Shetty SK, Shows HW, Hjelmaas AJ, Malcolm EK, Davies BS.
J Biol Chem 290(19):11865-77. doi: 10.1074/jbc.M114.623769. Epub 2015 Mar 25. 2015
4GPIHBP1, HYPL1D
Whole-exome sequencing reveals GPIHBP1 mutations in infantile colitis with severe hypertriglyceridemia.
Gonzaga-Jauregui C, Mir S, Penney S, Jhangiani S, Midgen C, Finegold M, Muzny DM, Wang M, Bacino CA, Gibbs RA, Lupski JR, Kellermayer R, Hanchard NA.
J Pediatr Gastroenterol Nutr 59(1):17-21. doi: 10.1097/MPG.0000000000000363. 2014
5GPIHBP1, HYPL1D
Familial chylomicronemia syndrome and response to medium-chain triglyceride therapy in an infant with novel mutations in GPIHBP1.
Ahmad Z, Wilson DP.
J Clin Lipidol 8(6):635-9. doi: 10.1016/j.jacl.2014.08.010. Epub 2014 Sep 9. 2014
6GPIHBP1
Endothelial cells respond to hyperglycemia by increasing the LPL transporter GPIHBP1.
Pei-Ling Chiu A, Wang F, Lal N, Wang Y, Zhang D, Hussein B, Wan A, Vlodavsky I, Rodrigues B.
Am J Physiol Endocrinol Metab 306(11):E1274-83. doi: 10.1152/ajpendo.00007.2014. Epub 2014 Apr 15. 2014
7GPIHBP1
The GPIHBP1-LPL complex is responsible for the margination of triglyceride-rich lipoproteins in capillaries.
Goulbourne CN, Gin P, Tatar A, Nobumori C, Hoenger A, Jiang H, Grovenor CR, Adeyo O, Esko JD, Goldberg IJ, Reue K, Tontonoz P, Bensadoun A, Beigneux AP, Young SG, Fong LG.
Cell Metab 19(5):849-60. doi: 10.1016/j.cmet.2014.01.017. Epub 2014 Apr 10. 2014
8GPIHBP1, LPL
Physiological regulation of lipoprotein lipase.
Kersten S.
Biochim Biophys Acta Jul;1841(7):919-33. doi: 10.1016/j.bbalip.2014.03.013. Epub 2014 Apr 8 2014
9GPIHBP1, LPL
Chylomicronemia mutations yield new insights into interactions between lipoprotein lipase and GPIHBP1.
Gin P, Goulbourne CN, Adeyo O, Beigneux AP, Davies BS, Tat S, Voss CV, Bensadoun A, Fong LG, Young SG.
Hum Mol Genet 21(13):2961-72. doi: 10.1093/hmg/dds127. Epub 2012 Apr 6. 2012
10GPIHBP1
Localization of lipoprotein lipase and GPIHBP1 in mouse pancreas: effects of diet and leptin deficiency.
Nyrén R, Chang CL, Lindström P, Barmina A, Vorrsjö E, Ali Y, Juntti-Berggren L, Bensadoun A, Young SG, Olivecrona T, Olivecrona G.
BMC Physiol 12:14. doi: 10.1186/1472-6793-12-14. 2012
11GPIHBP1, LPL
Mutations in lipoprotein lipase that block binding to the endothelial cell transporter GPIHBP1.
Voss CV, Davies BS, Tat S, Gin P, Fong LG, Pelletier C, Mottler CD, Bensadoun A, Beigneux AP, Young SG.
Proc Natl Acad Sci U S A 108(19):7980-4. Epub 2011 Apr 25. 2011
12GPIHBP1, HYPL1D
GPIHBP1 C89F neomutation and hydrophobic C-terminal domain G175R mutation in two pedigrees with severe hyperchylomicronemia.
Charrière S, Peretti N, Bernard S, Di Filippo M, Sassolas A, Merlin M, Delay M, Debard C, Lefai E, Lachaux A, Moulin P, Marçais C.
J Clin Endocrinol Metab 96(10):E1675-9. doi: 10.1210/jc.2011-1444. Epub 2011 Aug 3. 2011
13GPIHBP1, HYPL1D
Chylomicronemia with a mutant GPIHBP1 (Q115P) that cannot bind lipoprotein lipase.
Beigneux AP, Franssen R, Bensadoun A, Gin P, Melford K, Peter J, Walzem RL, Weinstein MM, Davies BS, Kuivenhoven JA, Kastelein JJ, Fong LG, Dallinga-Thie GM, Young SG.
Arterioscler Thromb Vasc Biol 29(6):956-62. doi: 10.1161/ATVBAHA.109.186577. Epub 2009 Mar 19. 2009
14GPIHBP1
Normal binding of lipoprotein lipase, chylomicrons, and apo-AV to GPIHBP1 containing a G56R amino acid substitution.
Gin P, Beigneux AP, Davies B, Young MF, Ryan RO, Bensadoun A, Fong LG, Young SG.
Biochim Biophys Acta 1771(12):1464-8. Epub 2007 Oct 22. 2007
15GPIHBP1
Homozygous missense mutation (G56R) in glycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1 (GPI-HBP1) in two siblings with fasting chylomicronemia (MIM 144650).
Wang J, Hegele RA.
Lipids Health Dis 6:23. 2007