Broiler chickens, bred for rapid growth, accumulate more fat under chronic heat stress, which reduces meat quality and ...

The familial chylomicronemia syndrome is a genetic disorder characterized by severe hypertriglyceridemia and recurrent pancreatitis due to a deficiency in lipoprotein lipase (LPL). Currently, there ...

A protein that is expressed on capillary endothelial cells, called GPIHBP1 (glycosylphosphatidylinositol-anchored high-density lipoprotein binding protein 1), binds lipoprotein lipase and shuttles ...

What Causes Familial Hyperchylomicronemia Syndrome? FCS happens because of a mutation in certain genes related to an enzyme called lipoprotein lipase (LpL). You have to get the mutated gene from ...

image: Lipoprotein lipase (LPL) mediates peripheral tissue triglyceride (TG) uptake. view more Credit: Yiliang Zhang, Shengyang Zhou, Runming Zhao, Yingzhen Huang, Yan Wang Living organisms store ...

Increasing HDL: Aerobic exercise stimulates the production of an enzyme called lipoprotein lipase (LPL), which raises HDL levels and breaks down fatty acids known as triglycerides that contribute ...

Alipogene tiparvovec contains the human lipoprotein lipase ("LPL") gene variant LPLS447X in a vector.

Zodasiran targets ANGPLT3, an emerging therapeutic target to treat HoFH and other dyslipidemias – YOSEMITE Phase 3 study further enhances Arrowhead’s late-stage pipeline o ...

The million dollar drug that patients can't access| The National Glybera was developed by Canadian scientists to treat a rare but devastating disease called lipoprotein lipase deficiency (LPLD).