| P50 | author | Alan T. Remaley | Q91944002 |
| P2093 | author name string | Adele Cooney | |
| | Christian A Combs | |
| | Edward B Neufeld | |
| | John A Stonik | |
| | Stephen J Demosky | |
| | H Bryan Brewer | |
| | Silvia Santamarina-Fojo | |
| | Nancy Dwyer | |
| | Catherine L Knapper | |
| | Joan Blanchette-Mackie | |
| | Marcella Comly | |
| P2860 | cites work | Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency | Q22010457 |
| | The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway | Q22010685 |
| | Apolipoprotein specificity for lipid efflux by the human ABCAI transporter | Q24290771 |
| | Defective endocytic trafficking of NPC1 and NPC2 underlying infantile Niemann-Pick type C disease | Q24293437 |
| | The two variants of oxysterol binding protein-related protein-1 display different tissue expression patterns, have different intracellular localization, and are functionally distinct | Q24554292 |
| | Human ATP-binding cassette transporter 1 (ABC1): genomic organization and identification of the genetic defect in the original Tangier disease kindred | Q24652427 |
| | Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1 | Q28141056 |
| | Preferential ATP-binding cassette transporter A1-mediated cholesterol efflux from late endosomes/lysosomes | Q28589822 |
| | THE DISTRIBUTION AND CHEMICAL COMPOSITION OF ULTRACENTRIFUGALLY SEPARATED LIPOPROTEINS IN HUMAN SERUM | Q29391553 |
| | Sorting of GPI-anchored proteins to glycolipid-enriched membrane subdomains during transport to the apical cell surface | Q29547857 |
| | The Niemann-Pick C1 protein resides in a vesicular compartment linked to retrograde transport of multiple lysosomal cargo | Q33856244 |
| | Late endosome motility depends on lipids via the small GTPase Rab7. | Q34078419 |
| | How cells handle cholesterol. | Q34094514 |
| | A PEST sequence in ABCA1 regulates degradation by calpain protease and stabilization of ABCA1 by apoA-I. | Q34827947 |
| | Cholesterol efflux to apolipoprotein AI involves endocytosis and resecretion in a calcium-dependent pathway | Q35648656 |
| | Defective removal of cellular cholesterol and phospholipids by apolipoprotein A-I in Tangier Disease | Q35749982 |
| | Subcellular localization and activity of multidrug resistance proteins | Q39855198 |
| | The ABCA1 transporter functions on the basolateral surface of hepatocytes | Q40700336 |
| | Helical apolipoproteins stabilize ATP-binding cassette transporter A1 by protecting it from thiol protease-mediated degradation | Q40738545 |
| | Evaluation of the role of phosphatidylserine translocase activity in ABCA1-mediated lipid efflux | Q40744769 |
| | Specific docking of apolipoprotein A-I at the cell surface requires a functional ABCA1 transporter | Q43517420 |
| | Cellular localization and trafficking of the human ABCA1 transporter | Q43604836 |
| | Acid sphingomyelinase-deficient macrophages have defective cholesterol trafficking and efflux | Q43752274 |
| | MLN64 mediates mobilization of lysosomal cholesterol to steroidogenic mitochondria | Q44031785 |
| | Synthetic amphipathic helical peptides promote lipid efflux from cells by an ABCA1-dependent and an ABCA1-independent pathway | Q44300047 |
| | The role of the ABCA1 transporter and cholesterol efflux in familial hypoalphalipoproteinemia | Q44406788 |
| | Cholesterol modulates membrane traffic along the endocytic pathway in sphingolipid-storage diseases | Q47622411 |
| | Transport of lipids from golgi to plasma membrane is defective in tangier disease patients and Abc1-deficient mice | Q47888259 |
| | Abnormal processing of Golgi elements and lysosomes in Tangier disease | Q70220055 |
| | Isolation and characterization of apolipoproteins A-I, A-II, and A-IV | Q70295451 |
| | Intracellular trafficking of cholesterol monitored with a cyclodextrin | Q71246519 |
| | Decreased reverse cholesterol transport from Tangier disease fibroblasts. Acceptor specificity and effect of brefeldin on lipid efflux | Q73780280 |
| | Use of BODIPY-labeled sphingolipids to study membrane traffic along the endocytic pathway | Q74786177 |
| P433 | issue | 15 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Apolipoprotein A1 | Q1316030 |
| | Tangier disease | Q1442621 |
| | ATP binding cassette subfamily A member 1 | Q21115210 |
| P304 | page(s) | 15571-8 | |
| P577 | publication date | 2004-04-09 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | The ABCA1 transporter modulates late endocytic trafficking: insights from the correction of the genetic defect in Tangier disease | |
| P478 | volume | 279 | |