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Publications by John J.P. Kastelein
Chylomicronemia With a Mutant GPIHBP1 (Q115P) That Cannot Bind Lipoprotein Lipase
Arteriosclerosis, Thrombosis, and Vascular Biology
Cardiovascular Medicine
Cardiology
Long-Term Correction of Murine Lipoprotein Lipase Deficiency With AAV1-Mediated Gene Transfer of the Naturally Occurring LPLS447XBeneficial Mutation
Human Gene Therapy
Molecular Medicine
Genetics
Molecular Biology
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Related publications
Structure of Lipoprotein Lipase in Complex With GPIHBP1
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Structure of the Lipoprotein Lipase–GPIHBP1 Complex That Mediates Plasma Triglyceride Hydrolysis
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Heterozygote of Lipoprotein Lipase Deficiency Presenting Chylomicronemia Syndrome
The Journal of Japan Atherosclerosis Society
Apo Structure of WT Lipoprotein Lipase in Complex With GPIHBP1 Mutant N78D N82D Produced in GnTI-deficient HEK293-F Cells
GPIHBP1 Is Responsible for the Entry of Lipoprotein Lipase Into Capillaries
Cell Metabolism
Cell Biology
Molecular Biology
Physiology
Cardiomyocyte VEGF Regulates Endothelial Cell GPIHBP1 to Relocate Lipoprotein Lipase to the Coronary Lumen During Diabetes MellitusSignificance
Arteriosclerosis, Thrombosis, and Vascular Biology
Cardiovascular Medicine
Cardiology
A Mutant P53 That Discriminates Between P53-Responsive Genes Cannot Induce Apoptosis.
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Equivalent Binding of Wild-Type Lipoprotein Lipase (LPL) and S447x-LPL to GPIHBP1, the Endothelial Cell LPL Transporter
Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids
Cell Biology
Molecular Biology
Heterogeneous Mutations in the Human Lipoprotein Lipase Gene in Patients With Familial Lipoprotein Lipase Deficiency.
Journal of Clinical Investigation
Medicine