Normal sorting but defective endocytosis of the low density lipoprotein receptor in mice with autosomal recessive hypercholesterolemia
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The modular adaptor protein ARH is required for low density lipoprotein (LDL) binding and internalization but not for LDL receptor clustering in coated pitsAMN directs endocytosis of the intrinsic factor-vitamin B(12) receptor cubam by engaging ARH or Dab2Secreted PCSK9 decreases the number of LDL receptors in hepatocytes and in livers of parabiotic miceCharacterization of the adaptor protein ARH expression in the brain and ARH molecular interactionsLow-density lipoprotein receptor (LDLR) family orchestrates cholesterol homeostasisProprotein convertase subtilisin/kexin type 9: from the discovery to the development of new therapies for cardiovascular diseasesAtomic structure of the autosomal recessive hypercholesterolemia phosphotyrosine-binding domain in complex with the LDL-receptor tailEndocytosis and Physiology: Insights from Disabled-2 Deficient MiceLow-density lipoprotein receptor-related protein interacts with MafB, a regulator of hindbrain developmentAdaptor protein ARH is recruited to the plasma membrane by low density lipoprotein (LDL) binding and modulates endocytosis of the LDL/LDL receptor complex in hepatocytesThe liver-selective thyromimetic T-0681 influences reverse cholesterol transport and atherosclerosis development in miceDifferent cellular traffic of LDL-cholesterol and acetylated LDL-cholesterol leads to distinct reverse cholesterol transport pathwaysDecreased plasma cholesterol and hypersensitivity to statins in mice lacking Pcsk9CCC- and WASH-mediated endosomal sorting of LDLR is required for normal clearance of circulating LDLA single common portal for clathrin-mediated endocytosis of distinct cargo governed by cargo-selective adaptors.The thyromimetic T-0681 protects from atherosclerosis.The endocytic adaptor protein ARH associates with motor and centrosomal proteins and is involved in centrosome assembly and cytokinesis.Cholesterol pathways affected by small molecules that decrease sterol levels in Niemann-Pick type C mutant cells.Cargo- and adaptor-specific mechanisms regulate clathrin-mediated endocytosis.The clathrin adaptor proteins ARH, Dab2, and numb play distinct roles in Niemann-Pick C1-Like 1 versus low density lipoprotein receptor-mediated cholesterol uptake.Casein kinase 2 phosphorylation of protein kinase C and casein kinase 2 substrate in neurons (PACSIN) 1 protein regulates neuronal spine formationGiardia lamblia low-density lipoprotein receptor-related protein is involved in selective lipoprotein endocytosis and parasite replication.Disruption of LDL but not VLDL clearance in autosomal recessive hypercholesterolemiaSorting it out: AP-2 and alternate clathrin adaptors in endocytic cargo selectionPathway-Wide Association Study Implicates Multiple Sterol Transport and Metabolism Genes in HDL Cholesterol Regulation.Quantitative fluorescence imaging reveals point of release for lipoproteins during LDLR-dependent uptake.S-nitrosylation of ARH is required for LDL uptake by the LDL receptor.Endocytic adaptors Arh and Dab2 control homeostasis of circulatory cholesterolARH directs megalin to the endocytic recycling compartment to regulate its proteolysis and gene expression.The ARH adaptor protein regulates endocytosis of the ROMK potassium secretory channel in mouse kidney.Identification of novel and known oocyte-specific genes using complementary DNA subtraction and microarray analysis in three different species.Post-transcriptional regulation of low density lipoprotein receptor protein by proprotein convertase subtilisin/kexin type 9a in mouse liver.Induction of MiR133a expression by IL-19 targets LDLRAP1 and reduces oxLDL uptake in VSMC.Internalized PCSK9 dissociates from recycling LDL receptors in PCSK9-resistant SV-589 fibroblastsRegulation of ApoB secretion by the low density lipoprotein receptor requires exit from the endoplasmic reticulum and interaction with ApoE or ApoB.The modular adaptor protein autosomal recessive hypercholesterolemia (ARH) promotes low density lipoprotein receptor clustering into clathrin-coated pits.Identification of a VLDL-induced, FDNPVY-independent internalization mechanism for the LDLR.Dissection of the endogenous cellular pathways of PCSK9-induced low density lipoprotein receptor degradation: evidence for an intracellular route.Atherogenic remnant lipoproteins: role for proteoglycans in trapping, transferring, and internalizing.Xenopus autosomal recessive hypercholesterolemia protein couples lipoprotein receptors with the AP-2 complex in oocytes and embryos and is required for vitellogenesis.
P2860
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P248
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P2860
Normal sorting but defective endocytosis of the low density lipoprotein receptor in mice with autosomal recessive hypercholesterolemia
description
2003 nî lūn-bûn
@nan
2003 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Normal sorting but defective e ...... recessive hypercholesterolemia
@ast
Normal sorting but defective e ...... recessive hypercholesterolemia
@en
Normal sorting but defective e ...... recessive hypercholesterolemia
@nl
type
label
Normal sorting but defective e ...... recessive hypercholesterolemia
@ast
Normal sorting but defective e ...... recessive hypercholesterolemia
@en
Normal sorting but defective e ...... recessive hypercholesterolemia
@nl
prefLabel
Normal sorting but defective e ...... recessive hypercholesterolemia
@ast
Normal sorting but defective e ...... recessive hypercholesterolemia
@en
Normal sorting but defective e ...... recessive hypercholesterolemia
@nl
P2093
P2860
P921
P356
P1476
Normal sorting but defective e ...... recessive hypercholesterolemia
@en
P2093
Christopher Jones
Helen H Hobbs
Joachim Herz
Jonathan C Cohen
Robert E Hammer
Wei-Ping Li
P2860
P304
P356
10.1074/JBC.M304855200
P407
P577
2003-08-01T00:00:00Z