Pages that link to "Q72903709"

The following pages link to The high density lipoprotein- and apolipoprotein A-I-induced mobilization of cellular cholesterol is impaired in fibroblasts from Tangier disease subjects (Q72903709):

Displaying 34 items.

• The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway (Q22010685) (← links)
• Human ATP-binding cassette transporter 1 (ABC1): genomic organization and identification of the genetic defect in the original Tangier disease kindred (Q24652427) (← links)
• Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1 (Q28141056) (← links)
• Intracellular cholesterol transport. (Q33601463) (← links)
• Accumulation of cardiolipin and lysocardiolipin in fibroblasts from Tangier disease subjects (Q34083473) (← links)
• High density lipoproteins and arteriosclerosis. Role of cholesterol efflux and reverse cholesterol transport (Q34123188) (← links)
• Caveolae and intracellular trafficking of cholesterol (Q34365129) (← links)
• Cellular cholesterol efflux (Q34455387) (← links)
• Genetic disorders associated with ATP binding cassette cholesterol transporters (Q34929699) (← links)
• Complete genomic sequence of the human ABCA1 gene: analysis of the human and mouse ATP-binding cassette A promoter (Q35173863) (← links)
• Defective removal of cellular cholesterol and phospholipids by apolipoprotein A-I in Tangier Disease (Q35749982) (← links)
• Cholesterol efflux as a critical component of Alzheimer's disease pathogenesis (Q35794571) (← links)
• The role of vesicular transport in ABCA1-dependent lipid efflux and its connection with NPC pathways (Q36331308) (← links)
• Role of apoA-I, ABCA1, LCAT, and SR-BI in the biogenesis of HDL. (Q36406570) (← links)
• Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes. (Q37271145) (← links)
• Defective regulation of phosphatidylcholine-specific phospholipases C and D in a kindred with Tangier disease. Evidence for the involvement of phosphatidylcholine breakdown in HDL-mediated cholesterol efflux mechanisms (Q37361499) (← links)
• Phenotype-dependent differences in apolipoprotein E metabolism and in cholesterol homeostasis in human monocyte-derived macrophages (Q37380814) (← links)
• Characterization of cholesterol homeostasis in telomerase-immortalized Tangier disease fibroblasts reveals marked phenotype variability. (Q37415602) (← links)
• The ABC transporters in lipid flux and atherosclerosis (Q37847270) (← links)
• ATP-binding cassette transporter A1: from metabolism to neurodegeneration (Q38213077) (← links)
• The pathology of cornea in Tangier disease (familial high density lipoprotein deficiency). (Q39587215) (← links)
• Stably transfected ABCA1 antisense cell line has decreased ABCA1 mRNA and cAMP-induced cholesterol efflux to apolipoprotein AI and HDL. (Q40757819) (← links)
• Induction of cellular cholesterol efflux to lipid-free apolipoprotein A-I by cAMP. (Q40958601) (← links)
• Stimulation of lipolysis enhances the rate of cholesterol efflux to HDL in adipocytes (Q42510228) (← links)
• The role of the ABCA1 transporter and cholesterol efflux in familial hypoalphalipoproteinemia (Q44406788) (← links)
• Can Tangier disease cause male infertility? A case report and an overview on genetic causes of male infertility and hormonal axis involved (Q47570178) (← links)
• Apolipoprotein binding to protruding membrane domains during removal of excess cellular cholesterol. (Q52538489) (← links)
• HDL3Stimulates Multiple Signaling Pathways in Human Skin Fibroblasts (Q71799257) (← links)
• High Density Lipoproteins Stimulate Mitogen-Activated Protein Kinases in Human Skin Fibroblasts (Q73780201) (← links)
• Novel mutations in ABCA1 gene in Japanese patients with Tangier disease and familial high density lipoprotein deficiency with coronary heart disease (Q74284486) (← links)
• Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations (Q74348218) (← links)
• Assignment of Tangier disease to chromosome 9q31 by a graphical linkage exclusion strategy (Q77220547) (← links)
• Genetics of lipoprotein disorders (Q77452737) (← links)
• Phospholipid transfer protein enhances removal of cellular cholesterol and phospholipids by high-density lipoprotein apolipoproteins (Q77968333) (← links)