Apolipoprotein C-II: New findings related to genetics, biochemistry, and role in triglyceride metabolism
A Wolska, RL Dunbar, LA Freeman, M Ueda, MJ Amar…�- Atherosclerosis, 2017 - Elsevier
Abstract Apolipoprotein C-II (apoC-II) is a small exchangeable apolipoprotein found on
triglyceride-rich lipoproteins (TRL), such as chylomicrons (CM) and very low-density�…
triglyceride-rich lipoproteins (TRL), such as chylomicrons (CM) and very low-density�…
Endothelial cell receptors in tissue lipid uptake and metabolism
NA Abumrad, AG Cabodevilla, D Samovski…�- Circulation�…, 2021 - Am Heart Assoc
Lipid uptake and metabolism are central to the function of organs such as heart, skeletal
muscle, and adipose tissue. Although most heart energy derives from fatty acids (FAs)�…
muscle, and adipose tissue. Although most heart energy derives from fatty acids (FAs)�…
[HTML][HTML] Beyond Lipoprotein (a) plasma measurements: Lipoprotein (a) and inflammation
G Reyes-Soffer, M Westerterp�- Pharmacological research, 2021 - Elsevier
Genome wide association, epidemiological, and clinical studies have established high
lipoprotein (a)[Lp (a)] as a causal risk factor for atherosclerotic cardiovascular disease�…
lipoprotein (a)[Lp (a)] as a causal risk factor for atherosclerotic cardiovascular disease�…
[HTML][HTML] Six years' experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemias
JS Dron, J Wang, AD McIntyre, MA Iacocca…�- BMC Medical�…, 2020 - Springer
Background In 2013, our laboratory designed a targeted sequencing panel,“LipidSeq”, to
study the genetic determinants of dyslipidemia and metabolic disorders. Over the last 6�…
study the genetic determinants of dyslipidemia and metabolic disorders. Over the last 6�…
The regulation of triacylglycerol metabolism and lipoprotein lipase activity
Y Wen, YQ Chen, RJ Konrad�- Advanced Biology, 2022 - Wiley Online Library
Triacylglycerol (TG) metabolism is tightly regulated to maintain a pool of TG within circulating
lipoproteins that can be hydrolyzed in a tissue‐specific manner by lipoprotein lipase (LPL) to�…
lipoproteins that can be hydrolyzed in a tissue‐specific manner by lipoprotein lipase (LPL) to�…
Inverse association between apolipoprotein C-II and cardiovascular mortality: role of lipoprotein lipase activity modulation
G Silbernagel, YQ Chen, M Rief…�- European Heart�…, 2023 - academic.oup.com
Abstract Aims Apolipoprotein C-II (ApoC-II) is thought to activate lipoprotein lipase (LPL) and
is therefore a possible target for treating hypertriglyceridemia. Its relationship with�…
is therefore a possible target for treating hypertriglyceridemia. Its relationship with�…
[HTML][HTML] Decoding the role of angiopoietin-like protein 4/8 complex–mediated plasmin generation in the regulation of LPL activity
YQ Chen, EY Zhen, AM Russell, M Ehsani…�- Journal of Lipid�…, 2023 - ASBMB
After feeding, adipose tissue lipoprotein lipase (LPL) activity should be maximized, therefore
the potent LPL-inhibitory activity of angiopoietin-like protein 4 (ANGPTL4) must be blocked�…
the potent LPL-inhibitory activity of angiopoietin-like protein 4 (ANGPTL4) must be blocked�…
Familial chylomicronemia syndrome: a rare but devastating autosomal recessive disorder characterized by refractory hypertriglyceridemia and recurrent pancreatitis
V Chyzhyk, AS Brown�- Trends in cardiovascular medicine, 2020 - Elsevier
Abstract Familial Chylomicronemia Syndrome (FCS) is a rare autosomal recessive lipid
disorder characterized by severe hypertriglyceridemia and recurrent pancreatitis. Because�…
disorder characterized by severe hypertriglyceridemia and recurrent pancreatitis. Because�…
[HTML][HTML] Hypertriglyceridemia and atherosclerosis: using human research to guide mechanistic studies in animal models
D Basu, KE Bornfeldt�- Frontiers in Endocrinology, 2020 - frontiersin.org
Human studies support a strong association between hypertriglyceridemia and
atherosclerotic cardiovascular disease (CVD). However, whether a causal relationship�…
atherosclerotic cardiovascular disease (CVD). However, whether a causal relationship�…
[HTML][HTML] Characterizing familial chylomicronemia syndrome: Baseline data of the APPROACH study
DJ Blom, L O'dea, A Digenio, VJ Alexander…�- Journal of clinical�…, 2018 - Elsevier
Background Familial chylomicronemia syndrome (FCS) is a rare metabolic disorder caused
by mutations in lipoprotein lipase (LPL) or genes required for LPL functionality and is�…
by mutations in lipoprotein lipase (LPL) or genes required for LPL functionality and is�…