An LPL–specific monoclonal antibody, 88B8, that abolishes the binding of LPL to GPIHBP1

GPIHBP1 and Plasma Triglyceride Metabolism

(2016) Loren G. Fong et al.   TRENDS IN ENDOCRINOLOGY AND METABOLISM

The acidic domain of the endothelial membrane protein GPIHBP1 stabilizes lipoprotein lipase activity by preventing unfolding of its catalytic domain

(2016) Simon Mysling et al.   eLife

Determination of serum lipoprotein lipase using a latex particle-enhanced turbidimetric immunoassay with an automated analyzer

(2015) Tetsuo Machida et al.   CLINICA CHIMICA ACTA

The GPIHBP1–LPL Complex Is Responsible for the Margination of Triglyceride-Rich Lipoproteins in Capillaries

(2014) Chris N. Goulbourne et al.   Cell Metabolism

Multimerization of Glycosylphosphatidylinositol-anchored High Density Lipoprotein-binding Protein 1 (GPIHBP1) and Familial Chylomicronemia from a Serine-to-Cysteine Substitution in GPIHBP1 Ly6 Domain

(2014) Wanee Plengpanich et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Whole-Exome Sequencing Reveals GPIHBP1 Mutations in Infantile Colitis With Severe Hypertriglyceridemia

(2014) Claudia Gonzaga-Jauregui et al.   JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION

Biochemistry and pathophysiology of intravascular and intracellular lipolysis

(2013) S. G. Young et al.   GENES & DEVELOPMENT

Novel Combined GPIHBP1 Mutations in a Patient with Hypertriglyceridemia Associated with CAD

(2013) Hiroyasu Yamamoto et al.   Journal of Atherosclerosis and Thrombosis

Assessing the Role of the Glycosylphosphatidylinositol-anchored High Density Lipoprotein-binding Protein 1 (GPIHBP1) Three-finger Domain in Binding Lipoprotein Lipase

(2011) Anne P. Beigneux et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

GPIHBP1 C89F Neomutation and Hydrophobic C-Terminal Domain G175R Mutation in Two Pedigrees with Severe Hyperchylomicronemia

(2011) Sybil Charrière et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Deletion of GPIHBP1 causing severe chylomicronemia

(2011) Jonathan J. Rios et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Childhood-onset chylomicronaemia with reduced plasma lipoprotein lipase activity and mass: identification of a novelGPIHBP1mutation

(2011) I. Coca-Prieto et al.   JOURNAL OF INTERNAL MEDICINE

Mutations in lipoprotein lipase that block binding to the endothelial cell transporter GPIHBP1

(2011) C. V. Voss et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Binding Preferences for GPIHBP1, a Glycosylphosphatidylinositol-Anchored Protein of Capillary Endothelial Cells

(2010) Peter Gin et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

GPIHBP1 Is Responsible for the Entry of Lipoprotein Lipase into Capillaries

(2010) Brandon S.J. Davies et al.   Cell Metabolism

Chylomicronemia With Low Postheparin Lipoprotein Lipase Levels in the Setting of GPIHBP1 Defects

(2010) Remco Franssen et al.   Circulation-Cardiovascular Genetics

Chylomicronemia With a Mutant GPIHBP1 (Q115P) That Cannot Bind Lipoprotein Lipase

(2009) Anne P. Beigneux et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

Highly Conserved Cysteines within the Ly6 Domain of GPIHBP1 Are Crucial for the Binding of Lipoprotein Lipase

(2009) Anne P. Beigneux et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia

(2009) Gunilla Olivecrona et al.   JOURNAL OF LIPID RESEARCH