Mutations in the ANGPTL3 Gene and Familial Combined Hypolipidemia: A Clinical and Biochemical Characterization

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  11. Antibodies to human angiopoietin-like protein 3: a patent evaluation of WO2012174178
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  17. Familial combined hypolipidemia due to mutations in theANGPTL3gene
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  18. Genetics of familial hypercholesterolemia: a tool for development of novel lipid lowering pharmaceuticals?
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  21. ANGPTL3 Mutations in Unrelated Chinese Han Patients with Familial Hypercholesterolemia
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  22. Genetically determined deficiency of ANGPTL3 does not alter HDL ability to preserve endothelial homeostasis
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  39. Genetic Disorders of HDL Metabolism
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  43. Breaking barriers: Innovative therapies for managing homozygous familial hypercholesterolemia
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  44. ANGPTL3 nanobody-FGF21 fusion protein ameliorates metabolic dysfunction-associated fatty liver disease via regulation of lipid and glucose metabolism and attenuation of oxidative stress
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  45. Hepatocyte-Specific Knockout of YAP Protects Against Atherosclerosis via Inhibition of ANGPTL3 in Mice
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  47. Human Angiopoietin-like Protein 3/ANGPTL3 Antibodies: Adding to the Armamentarium in the Management of Dyslipidemia
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