| scholarly article | Q13442814 |
| P356 | DOI | 10.1161/01.ATV.19.3.802 |
| P698 | PubMed publication ID | 10073989 |
| P2093 | author name string | G Ricci | |
| S Fazio | |||
| A Signore | |||
| A Montali | |||
| M Arca | |||
| G Bader | |||
| M Chianelli | |||
| R Fellin | |||
| F Campagna | |||
| S Bellosta | |||
| A Pacifico | |||
| M Maioli | |||
| G Zuliani | |||
| P433 | issue | 3 | |
| P304 | page(s) | 802-809 | |
| P577 | publication date | 1999-03-01 | |
| P1433 | published in | Arteriosclerosis, Thrombosis, and Vascular Biology | Q4797542 |
| P1476 | title | Characterization of a new form of inherited hypercholesterolemia: familial recessive hypercholesterolemia | |
| P478 | volume | 19 |
| Q34145054 | A new locus for autosomal recessive hypercholesterolemia maps to human chromosome 15q25-q26 |
| Q28298386 | A novel ARH splice site mutation in a Mexican kindred with autosomal recessive hypercholesterolemia |
| Q30478248 | A single common portal for clathrin-mediated endocytosis of distinct cargo governed by cargo-selective adaptors |
| Q24306476 | ARH is a modular adaptor protein that interacts with the LDL receptor, clathrin, and AP-2 |
| Q28564763 | Association of the low-density lipoprotein receptor with caveolae in hamster and rat liver |
| Q28207619 | Autosomal recessive hypercholesterolaemia in Sardinia, Italy, and mutations in ARH: a clinical and molecular genetic analysis |
| Q28204109 | Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH gene |
| Q35196188 | Benefits and risks of simvastatin in patients with familial hypercholesterolaemia |
| Q33435708 | Carboxy-terminal deletion of the HDL receptor reduces receptor levels in liver and steroidogenic tissues, induces hypercholesterolemia, and causes fatal heart disease |
| Q75239559 | Clinical and biochemical characterisation of patients with autosomal recessive hypercholesterolemia (ARH) |
| Q35250984 | Disruption of LDL but not VLDL clearance in autosomal recessive hypercholesterolemia |
| Q24621515 | Exogenous plant MIR168a specifically targets mammalian LDLRAP1: evidence of cross-kingdom regulation by microRNA |
| Q64060780 | Functional Segments on Intrinsically Disordered Regions in Disease-Related Proteins |
| Q74252638 | Genetic characterization of Swedish patients with familial hypercholesterolemia: a heterogeneous pattern of mutations in the LDL receptor gene |
| Q36089523 | Genetic lipoprotein disorders and coronary atherosclerosis |
| Q42112172 | Identification of a VLDL-induced, FDNPVY-independent internalization mechanism for the LDLR. |
| Q38713991 | Induction of MiR133a expression by IL-19 targets LDLRAP1 and reduces oxLDL uptake in VSMC. |
| Q36708971 | Influence of PDZK1 on lipoprotein metabolism and atherosclerosis |
| Q35938094 | LDL-receptor mutations in Europe |
| Q30942732 | Loss of PDZK1 causes coronary artery occlusion and myocardial infarction in Paigen diet-fed apolipoprotein E deficient mice |
| Q27003094 | Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk |
| Q43613380 | Molecular medicine. The cholesterol quartet |
| Q28363810 | Monogenic dyslipidemias: window on determinants of plasma lipoprotein metabolism |
| Q28204028 | Normal Sorting but Defective Endocytosis of the Low Density Lipoprotein Receptor in Mice with Autosomal Recessive Hypercholesterolemia |
| Q34774354 | Peroxisome proliferator-activated receptor agonists, hyperlipidaemia, and atherosclerosis. |
| Q24323051 | Restoration of LDL receptor function in cells from patients with autosomal recessive hypercholesterolemia by retroviral expression of ARH1 |
| Q33767978 | Role of the adaptor protein PDZK1 in controlling the HDL receptor SR-BI |
| Q36822549 | S-nitrosylation of ARH is required for LDL uptake by the LDL receptor |
| Q28208721 | Targeted Disruption of the PDZK1 Gene in Mice Causes Tissue-specific Depletion of the High Density Lipoprotein Receptor Scavenger Receptor Class B Type I and Altered Lipoprotein Metabolism |
| Q47155313 | The Genetic Spectrum of Familial Hypercholesterolemia (FH) in the Iranian Population |
| Q24321718 | The autosomal recessive hypercholesterolemia (ARH) protein interfaces directly with the clathrin-coat machinery |
| Q34580436 | 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. |
| Q24294525 | The modular adaptor protein ARH is required for low density lipoprotein (LDL) binding and internalization but not for LDL receptor clustering in coated pits |
| Q38381808 | The promise of proprotein convertase subtilisin/kexin 9 inhibitors for the treatment of familial hypercholesterolemia |
Search more.