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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Aug 2016.

Lipoprotein lipase

Lipoprotein Lipase, LPL
Top mentioned proteins: ACID, HAD, CAN, Insulin, HDL
Papers using Lipoprotein Lipase antibodies
Effect of adipocyte beta3-adrenergic receptor activation on the type 2 diabetic MKR mice
Supplier
Luque Raul M., In PLoS ONE, 2005
... antibody (Cell Signaling Technology, Danvers, MA); mouse monoclonal lipoprotein lipase (LPL) antibody, and rabbit polyclonal HSL antibody (Abcam Inc, Cambridge, MA) ...
Molecular dissection of ligand binding sites on the low density lipoprotein receptor-related protein
Supplier
Pedrini Michael T. et al., In Molecular and Cellular Endocrinology, 1993
... anti-GSK-3 (anti-glycogen synthase kinase 3) antibody was obtained from Upstate (Charlottesville, VA, USA) and the LPL antibody from Abcam (Cambridge, UK); anti-phospho-GSK-3/β-ser21/9, anti-phospho-Akt-ser473 ...
Papers on Lipoprotein Lipase
Interaction of lipoprotein lipase polymorphisms with body mass index and birth weight to modulate lipid profiles in children and adolescents: the CASPIAN-III Study.
New
Kelishadi et al., Eşfahān, Iran. In Sao Paulo Med J, Feb 2016
This study aimed to determine to what extent variants of lipoprotein lipase (LPL) might interact with birth weight or body weight in determining the lipid profile concentrations in children and adolescents.
Inhibition by Seeds of Phalaris canariensis Extracts of Key Enzymes Linked to Obesity.
New
Cruz Victoria et al., In Altern Ther Health Med, Jan 2016
Lipoprotein lipase (LPL) activity was measured by released (3H)-oleic acid.
Expression of lipases and lipid receptors in sperm storage tubules and possible role of fatty acids in sperm survival in the hen oviduct.
New
Yoshimura et al., Hiroshima, Japan. In Theriogenology, Jan 2016
Expression of genes encoding endothelial lipase (EL), lipase H (LIPH), adipose triglyceride lipase (ATGL), and lipoprotein lipase (LPL) were found in UVJ.
Disturbances in apoptosis of lamina propria lymphocytes in Crohn's disease.
New
Linke et al., Poznań, Poland. In Arch Med Sci, Jan 2016
INTRODUCTION: The aim of this study was to assess the potential mechanisms providing resistance to apoptosis of lamina propria lymphocytes (LPL) directlyin intestinal tissues from patients with Crohn's disease (CD).
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.
New
Valladares-Salgado et al., Houston, United States. In Sci Rep, Dec 2015
Genome-wide significant signals were observed in or near CELSR2, ZNF259/APOA5, KANK2/DOCK6 and NCAN/MAU2 for total cholesterol, LPL, ABCA1, ZNF259/APOA5, LIPC and CETP for HDL cholesterol, CELSR2, APOB and NCAN/MAU2 for LDL cholesterol, and GCKR, TRIB1, ZNF259/APOA5 and NCAN/MAU2 for triglycerides.
Update on the molecular biology of dyslipidemias.
Review
New
Ramasamy, Worcester, United Kingdom. In Clin Chim Acta, Dec 2015
Monogenic hypertriglyceridemia is the result of mutations in genes that regulate the metabolism of triglyceride rich lipoproteins (eg LPL, APOC2, APOA5, LMF1, GPIHBP1).
The many faces of small B cell lymphomas with plasmacytic differentiation and the contribution of MYD88 testing.
Review
New
Campo et al., Pittsburgh, United States. In Virchows Arch, Nov 2015
UNASSIGNED: Plasmacytic differentiation may occur in almost all small B cell lymphomas (SBLs), although it varies from being uniformly present (as in lymphoplasmacytic lymphoma (LPL)) to very uncommon (as in mantle cell lymphomas (MCLs)).
Association of Genetic Variants with Polypoidal Choroidal Vasculopathy: A Systematic Review and Updated Meta-analysis.
Review
New
Chen et al., Hong Kong, Hong Kong. In Ophthalmology, Sep 2015
Another 25 polymorphisms in 13 genes (ARMS2, HTRA1, C2, CFB, ELN, LIPC, LPL, ABCA1, VEGF-A, TLR3, LOXL1, SERPING1, and PEDF) had no significant association.
Treatment of primary hypertriglyceridemia states--General approach and the role of extracorporeal methods.
Review
New
Julius et al., Roma, Italy. In Atheroscler Suppl, May 2015
In children and adults a genetic cause may underlie HTG which can be expressed as CMs a severe clinical picture known as Familial Hyperchylomicronemia due to lipoprotein lipase (LPL) or apolipoprotein (apo) CII deficiencies.
Targeting APOC3 in the familial chylomicronemia syndrome.
Impact
Witztum et al., Montréal, Canada. In N Engl J Med, 2015
The familial chylomicronemia syndrome is a genetic disorder characterized by severe hypertriglyceridemia and recurrent pancreatitis due to a deficiency in lipoprotein lipase (LPL).
Intravascular large B-cell lymphoma secondary to lymphoplasmacytic lymphoma: a case report and review of literature with clonality analysis.
Review
Tobinai et al., Tokyo, Japan. In Int J Clin Exp Pathol, 2014
Lymphoplasmacytic lymphoma (LPL) is an indolent B-cell lymphoma accompanied by monoclonal immunoglobulin M protein in most patients, and known to be associated with high risk of secondary hematological malignancies.
The ER-associated degradation adaptor protein Sel1L regulates LPL secretion and lipid metabolism.
Impact
Qi et al., Ithaca, United States. In Cell Metab, 2014
Further analyses reveal that Sel1L is indispensable for the secretion of lipoprotein lipase (LPL), independent of its role in Hrd1-mediated ERAD and ER homeostasis.
The GPIHBP1-LPL complex is responsible for the margination of triglyceride-rich lipoproteins in capillaries.
Impact
Fong et al., Los Angeles, United States. In Cell Metab, 2014
Triglyceride-rich lipoproteins (TRLs) undergo lipolysis by lipoprotein lipase (LPL), an enzyme that is transported to the capillary lumen by an endothelial cell protein, GPIHBP1.
Circulating angiopoietin-like 4 links proteinuria with hypertriglyceridemia in nephrotic syndrome.
Impact
Chugh et al., Birmingham, United States. In Nat Med, 2014
But at the same time, in a local feedback loop, the elevated extrarenal pools of Angptl4 reduced tissue FFA uptake in skeletal muscle, heart and adipose tissue, subsequently resulting in hypertriglyceridemia, by inhibiting lipoprotein lipase (LPL)-mediated hydrolysis of plasma triglycerides to FFAs.
A largely random AAV integration profile after LPLD gene therapy.
Impact
Schmidt et al., Heidelberg, Germany. In Nat Med, 2013
We performed integration-site analysis after AAV1-LPL(S447X) intramuscular injection in five lipoprotein lipase-deficient subjects, revealing random nuclear integration and hotspots in mitochondria.
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