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«ABCA1

Below is an extended ABCA1 publications listing. Click here to return to the gene page.

Gene Information from Publications

Publication Link Summary of findings
18097620 Observational study of gene-disease association. (HuGE Navigator)
18199144 Observational study of gene-disease association. (HuGE Navigator)
18215356 Observational study of gene-disease association and pharmacogenomic / toxicogenomic. (HuGE Navigator)
18219093 Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator)
18239666 Observational study of gene-disease association. (HuGE Navigator)
18354102 Observational study of gene-disease association. (HuGE Navigator)
17481640 ABCA1 expression in human leukocytes and muscle is associated with physical activity and alcohol consumption, respectively
17550732 Observational study of gene-disease association. (HuGE Navigator)
17553166 Observational study of gene-disease association. (HuGE Navigator)
17608096 Observational study of gene-disease association. (HuGE Navigator)
17700364 Observational study of gene-disease association and pharmacogenomic / toxicogenomic. (HuGE Navigator)
17855807 Observational study of gene-disease association. (HuGE Navigator)
17923263 Observational study of gene-disease association. (HuGE Navigator)
17951323 Observational study of gene-disease association. (HuGE Navigator)
18003760 Observational study of gene-disease association. (HuGE Navigator)
18164264 Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator)
11238261 Observational study of gene-disease association. (HuGE Navigator)
11257261 Observational study of gene-disease association. (HuGE Navigator)
11349008 Observational study of gene-disease association and gene-environment interaction. (HuGE Navigator)
11809185 Observational study of gene-disease association. (HuGE Navigator)
11940086 Observational study of gene-disease association. (HuGE Navigator)
12535741 Observational study of gene-disease association. (HuGE Navigator)
12600975 Observational study of gene-disease association. (HuGE Navigator)
12624133 Observational study of gene-disease association. (HuGE Navigator)
12700893 Observational study of gene-disease association. (HuGE Navigator)
12860256 Observational study of gene-disease association. (HuGE Navigator)
12870173 Observational study of gene-disease association. (HuGE Navigator)
14767869 Observational study of gene-disease association. (HuGE Navigator)
14962947 Observational study of gene-disease association. (HuGE Navigator)
14986172 Observational study of gene-disease association. (HuGE Navigator)
15024730 Observational study of gene-disease association. (HuGE Navigator)
15135251 Observational study of gene-disease association. (HuGE Navigator)
15201080 Observational study of gene-disease association. (HuGE Navigator)
15262183 Observational study of gene-disease association. (HuGE Navigator)
15288432 Observational study of gene-disease association. (HuGE Navigator)
15297675 Observational study of gene-disease association. (HuGE Navigator)
15340333 Observational study of genotype prevalence and gene-disease association. (HuGE Navigator)
15500734 Observational study of gene-disease association. (HuGE Navigator)
15520867 Observational study of gene-disease association. (HuGE Navigator)
15528481 Observational study of gene-disease association. (HuGE Navigator)
15649702 Observational study of gene-disease association. (HuGE Navigator)
15657615 Observational study of gene-disease association. (HuGE Navigator)
15696473 Observational study of genotype prevalence. (HuGE Navigator)
15721294 Observational study of gene-disease association. (HuGE Navigator)
15829498 Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator)
15935359 Observational study of genotype prevalence and gene-disease association. (HuGE Navigator)
15952113 Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator)
15958302 Observational study of gene-disease association. (HuGE Navigator)
16030523 Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator)
16080812 Observational study of gene-disease association. (HuGE Navigator)
16086925 Observational study of gene-disease association. (HuGE Navigator)
16120575 Observational study of gene-disease association. (HuGE Navigator)
16157450 Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator)
16226177 Observational study of gene-disease association. (HuGE Navigator)
16313984 Observational study of gene-disease association. (HuGE Navigator)
16446539 Observational study of gene-disease association. (HuGE Navigator)
16542392 Observational study of gene-disease association. (HuGE Navigator)
16596262 Observational study of gene-disease association. (HuGE Navigator)
16725228 Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator)
16763159 Observational study of gene-disease association. (HuGE Navigator)
16770077 Observational study of gene-disease association. (HuGE Navigator)
16806540 Observational study of gene-disease association. (HuGE Navigator)
16879828 Observational study of gene-disease association. (HuGE Navigator)
17001213 Observational study of gene-disease association and gene-environment interaction. (HuGE Navigator)
17113061 Observational study of gene-disease association. (HuGE Navigator)
17135600 Observational study of gene-disease association and gene-environment interaction. (HuGE Navigator)
17268197 Observational study of gene-disease association and gene-environment interaction. (HuGE Navigator)
17324514 Observational study of gene-disease association. (HuGE Navigator)
17335784 Observational study of gene-disease association. (HuGE Navigator)
17368464 Observational study of gene-disease association. (HuGE Navigator)
17372331 Observational study of gene-disease association. (HuGE Navigator)
17383594 Observational study of gene-disease association. (HuGE Navigator)
17407076 Observational study of gene-disease association. (HuGE Navigator)
17412755 Observational study of gene-disease association. (HuGE Navigator)
12709788 Observational study of gene-disease association. (HuGE Navigator)
17430597 Observational study of gene-disease association. (HuGE Navigator)
18097620 These results suggest that polymorphisms of ABCA1 and ROS1 are determinants of blood pressure and the development of hypertension in Japanese individuals.
18220685 ABC-A1 may be more than a determinant of HDL-cholesterol which may provide a link between components of the metabolic syndrome and atherosclerosis.
17992631 The interaction of ABCA1 with AOX1 modulates ABCA1-linked cellular functions such as lipid efflux and phagocytosis in hepatocytes (HC), and reduced expression of AOX1 in malignant transformed HC supports the differentiation dependent upregulation of AOX1.
17510949 Intronic polymorphism of ABCA1 gene is associated with sporadic Alzheimer's disease
17412755 an influence of common ABCA1 functional polymorphisms on age of symptom onset in coronary artery disease patients
18199144 Mutations were identified in 5 low-HDL subjects. 4 SNPs in ABCA1 gene promoter identified the C-14T SNP & the TCCT haplotype to be over-represented in low-HDL individuals. Sequence variation in ABCA1 contributes significantly to variation in HDL levels.
17689273 Results revealed that TNF-alpha could increase cholesterol content by down-regulating ABCA1 expression, IL-10 time-dependently decreased cholesterol accumulation by up-regulating ABCA1 expression.
17951323 3 of 6 nonsynonymous single nucleotide polymorphisms in ATP-binding cassette sub-family A (ABC1) member 1 (ABCA1) predict risk of ischemic heart disease in the general population.
17656736 Our results provide a biochemical basis for the HDL biogenesis pathway that involves both ABCA1 and the "high-capacity binding site", supporting a two binding site model for ABCA1-mediated nascent HDL genesis.
17690481 results indicate that ABCG5/G8, unlike ABCA1, together with bile acids should participate in sterol efflux on the apical surface of Caco-2 cells.
17510946 the relationship between ABCA1 genetic variants and Alzheimer's disease (AD), independently or in concert with the APOE epsilon4 allele
17368464 analysis of genetic variation in the ATP-binding cassette transporter A1, plasma lipids, and risk of coronary heart disease
17923263 R219K polymorphism of ABCA1 related with low HDL in overweight/obese Thai males.
17556657 Doxazosin inhibits AP2alpha activity independent of alpha(1)-adrenoceptor blockade and increases the ABCA1 expression and HDL biogenesis
17070530 ABCA1 polymorphism is associated with the pathogenesis of coronary heart disease in Germany.
17372331 Results suggest that defective ABCA1 function in cholesterol-loaded macrophages is one potential contributor to the impaired reverse cholesterol transport process and the increased coronary heart disease risk in subjects with familial low HDL.
12196520 A novel serine (Ser-2054) on the ABCA1 protein crucial for PKA phosphorylation and for regulation of ABCA1 transporter activity.
15024730 Several single nucleotide polymorphisms spanning the ABCA1 gene modify Alzheimer disease risk.
12870173 results indicate that the K219 allele frequency of adenosine triphosphate binding cassette transporter 1 differs markedly between blacks and whites
15492319 ABCA1 is not required for apolipoprotein A-1-mediated endothelial cholesterol efflux from vascular endothelial cells.
15066991 ABCA1 is not requied for a positive feedback pathway for stimulation of potentially anti-atherogenic apoE secretion by alpha-helix-containing molecules including apoA-I and apoE
16596262 data support the observation that ABCA1 polymorphisms influence cholesterol metabolism of the brain, but might not act as a major risk factor in Alzheimer's disease.
17268197 ABCA1 gene I823M polymorphism altered plasma HDL-C level and also modified the effect of low-HDL-C on the risk of CAD.
17521614 Taken together, the current study demonstrates that APN might protect against atherosclerosis by increasing HDL assembly through enhancing ABCA1 pathway and apoA-1 synthesis in the liver.
12151852 REVIEW: ATP-binding cassette transporter A1 and cholesterol trafficking
16709568 Fluorescence resonance energy transfer and native plyacrylamide gel electrophoresis analytical techniques were employed to assess the quaternary structure of ABCA1
17135302 ROS and NF-kappaB, but not LXR, mediate the IL-1beta-induced downregulation of ABCA1 via a novel transcriptional mechanism, which might play an important role of proinflammation in the alteration of lipid metabolism.
17287470 This is the first study reporting the association of the ATP-binding cassette transporter A1 R230C variant with obesity and obesity-related comorbidities in the Mexican population.
14734645 ApoA-1 removes excess cholesterol & phospholipids from macrophages by an active pathway involving ABCA1. The slow component of this efflux is the ABCA1-dependent process.
14576201 ABCA1 gene sequence in a proband with very low HDL cholesterol and premature coronary heart disease family history revealed 2 mutations: G5947A (R1851Q) and single thymidine deletion in a polypyrimidine tract 33 to 46 bps upstream from start of exon 47
16118212 intracellular unsaturated acyl-CoA derivatives destabilize ABCA1 by activating a PLD2 signaling pathway
15469992 ABCA1 forms a complex with syntaxin 13 and flotillin-1, residing at the plasma membrane and in phagosomes
16902247 ABCG1 and ABCG4 act in concert with ABCA1 to maximize the removal of excess cholesterol from cells and to generate cholesterol-rich lipoprotein particles
16928680 hepatic overexpression of ABCA1 in low density lipoprotein receptor-KO mice leads to: 1) expansion of the pro-atherogenic apoB-lipoprotein cholesterol pool size via enhanced transfer of HDL-cholesterol to apoB-lipoproteins
15163665 conclude that intact ATP binding cassette transporter A1 (ABCA1) function is necessary for proper maturation of dense bodies in platelets
15961705 dramatic decrease of ABCA1 protein, the key molecule of cholesterol efflux, in atheroma
11855831 contributes to the secretion of interleukin 1beta from macrophages
14967823 increased palmitate and stearate desaturation by stearoyl-CoA desaturase was associated with the destabilization of ABCA1 by saturated fatty acids palmitate and stearate
16343503 Approximately 20% of French-Canadian patients with severe HDL deficiency are associated with a defective ABCA1.
14767869 the K219 allele of the ABCA1 gene is an anti-atherogenic allele with increased cholesterol efflux activity
15292375 apoA-I mobilizes intracellular cholesterol for the ABCA1-mediated release from the compartment that is under the control of ACAT. The cholesterol mobilization process is presumably related to PKC activation by apoA-I.
15358760 SREBP2 down-regulates ATP-binding cassette transporter A1 in vascular endothelial cells
16855366 REVIEW: the presence of ABCA1 and ABCG1 in the AP-3 pathway will have major impact for membrane phospholipid processing and HDL metabolism and their relation to disorders of lysosome-related organelles
15297675 tested whether rare sequence variants of ABCA1, APOA1, and LCAT collectively contribute to variation in plasma levels of high density lipoprotein cholesterol; nonsynonymous sequence variants were significantly more common in individuals with low HDL-C
15528463 We propose that the decreased level of ABCA1 protein is a key factor in the development of atherosclerotic lesions.
15528481 The ABCA1 gene -565C>T polymorphism was associated with coronary atherosclerosis severity. This variant had an effect on ABCA1 promoter activity. Common ABCA1 variants contribute to interindividual variability in atherosclerosis susceptibility & severity.
12084722 ABCA1 mutations can disrupt its direct interaction with apolipoprotein A-I.
12562845 examine the necessary structural features for a protein to promote lipid efflux by the ABCA1 transporter and find the amphipathic helix is a key structural motif for peptide-mediated lipid efflux from ABCA1, but there is no stereoselective requirement
12804586 regulation of ABCA1 mRNA levels exploits the use of alternative transcription start sites
14644402 Of special interest was our finding that the effects of compromised ABCA1 function on HDL were more pronounced in women than in men.
14701812 HDL(3) promotes ABCA1-mediated lipid efflux entirely through its lipid-poor fraction with pre-beta mobility
14701824 the ABCA1 transporter has a role in cellular cAMP signaling with Apolipoprotein A-I
14701850 an amphiphilic helical motif is the minimum structural requirement for a protein to stabilize ABCA1 against proteolytic degradation
15102890 The reciprocal inhibition of SR-BI and ABCA1 by BLT-4 and glyburide raises the possibility that these proteins may share similar or common steps in their mechanisms of lipid transport.
11950847 Helical apolipoproteins stabilize ATP-binding cassette transporter A1 by protecting it from thiol protease-mediated degradation.
12204794 Recent data confirms that a single defective allele in ABCA1 may be assosiated with reduced HDL cholesterol and FHA.
16055210 An amino acid substitution in ABCA1 is associated with low levels of HDL and diabetes mellitus, type 2.
16254209 Glucocorticoid receptor ligands affected ABCA1 expression and cholesterol efflux from macrophages
14747463 ABCA1 converts pools of late endocytic lipids that retain NPC1 to pools that can associate with endocytosed apoA-I, and be released from the cell as nascent high density lipoprotein
15930518 The ABCA1-mediated reaction produced two distinct HDLs, large cholesterol-rich and small cholesterol-poor particles, and the former is more prominently dependent on the increase of ABCA1 expression
12111371 R1680W mutation associated with Tangier disease, phenotypes variable.
12235128 The association of FADD with ABCA1 provides an unexpected link between high density lipoprotein metabolism and an adaptor molecule mainly described in death receptor signal transduction.
16235041 A review of functions and mutations of ABCA1 in Tangier disease.
16126721 the ABCA1 pathway is impaired by acrolein-induced apoA-I modification
16418537 Results show that the products of the apoA-I/ABCA1 interaction include discoidal HDL particles containing different numbers of apoA-I molecules.
16429166 Impact of genetic variation on ABCA1 function.
12763760 In this study we review how genetic variation at the ABCA1 locus affects its role in the maintenance of lipid homeostasis and the natural progression of atherosclerosis.
14967052 A two step model of cholesterol efflux is suggested that can explain the functional interactions of ABCA1 with apoA-I and other cholesterol acceptors, based on formation of a tight complex between ABCA1 and its ligands.
14993242 ABCA1 does not differentiate between cholesterol and beta-sitosterol and thus is not responsible for the selectivity of sterol absorption by the intestine
12730295 hepatic overexpression of ABCA1 showed a selective increase in HDL cholesterol
15140889 probucol inactivates ABCA1 in the plasma membrane with respect to its function in mediating binding of and lipid release by apolipoprotein and with respect to proteolytic degradation by calpain
15358117 Serum amyloid A promotes ABCA1-dependent and ABCA1-independent lipid efflux from cells.
15520867 ABC transporter A1 has a role in regulating levels of HDL cholesterol
11861672 a novel site in the human ABCA1 promoter involved in the regulation of ABCA1 gene expression.
15574409 apolipoprotein A-I chlorination markedly impairs ABCA1-dependent cholesterol transport
16166555 mABC1 protein plays a major role in cellular protection against oxidant stress.
16313984 ABCA! polymorphisms and prognosis after myocardial infarction were analyzed in a young male cohort.
16410457 ABCA1-mediated efflux to serum responds to the pool of lipid-free/poor apolipoproteins
16500904 analysis of the biochemical basis of the mechanism for HDL formation mediated by ABCA1
16730733 Suppression of both the ABCA1 and ABCG1 genes may indicate that unsaturated fatty acids suppress not only cholesterol efflux to apoA-I and thereby nascent HDL formation but also HDL-dependent cholesterol efflux from vascular cells.
17020879 NPC1 protein function is non-essential for the trafficking and removal of cellular cholesterol by ApoAI if the down-stream defects in ABCA1 and ABCG1 regulation in NPC disease cells are corrected using an LXR agonist
17082211 Two genes of the cholesterol efflux system (ABCA1 and ABCG1) were down-regulated in HCAECs exposed to uraemic plasma.
14962947 Two polymorphisms were associated with plasma levels of ApoA1, 1 in the promoter (C-564T) and 1 in the coding (R1587K) regions, whereas only 1 polymorphism (R219K) was associated with the risk of myocardial infarction.
11700048 function as a regulator rather than an active transporter
12093886 Increased ABCA1 activity protects against atherosclerosis. ABCA1(human transgenic)(+)ApoE(-/-) mice developed dramatically smaller, less-complex lesions as compared with their ApoE(-/-) counterparts.
14754908 ABCA1 is essential for the biogenesis of high density-sized lipoprotein containing only apoE particles in vivo
15774904 Catalytic subunits of SWI/SNF chromatin remodeling complex, BRG-1 and brahma, play significant roles in enhancing LXR/RXR-mediated transcription of ABCA1 via the promoter DR-4 element
15951431 the internalization and trafficking of ABCA1 is functionally important in mediating cholesterol efflux from intracellular cholesterol pools
14986172 ABCA1 G(-273)C polymorphism has a significant effect on the HDL-C level in the general Japanese population, but not on the incidence of myocardia infarction
16192269 beta1-syntrophin acts through a class-I PDZ interaction with the C terminus of ABCA1 to regulate the cellular distribution and activity of the transporter
12813037 ABCA1 has a role in the low levels of HDL-cholesterol and overaccumulation of cellular lipids in Niemann-Pick Disease type C
15280376 the majority of ABCA1 exists as a tetramer that binds apoA; the homotetrameric ABCA1 complex constitutes the minimum functional unit required for the biogenesis of high density lipoprotein particles.
12709788 While genotype-phenotype associations were not reproduced across populations and loci, V825I and M883I were clearly associated with coronary artery disease status in Malays with no effects on HDL-C or apoA1.
12615681 Review. Transgenic mice with human ABCA1 genes are used to study its function in cholesterol transport, apo B lipoproteins, and atherosclerosis.
14681836 first demonstration of an association between ATP-binding cassette, sub-family A member 1 gene expression and fasting glucose concentration in vivo
15905177 analysis of headgroup-specific exposure of phospholipids in ABCA1-expressing cells
15983222 Glycolaldehyde and glyoxal strongly inhibited ABCA1-dependent transport of cholesterol from cells to apoA-I, while methylglyoxal had little effect.
11893753 Role as a phosphatidylserine translocase
14668333 results suggest that the interaction of apolipoproteins with ATP binding cassette transporter A1(ABCA1)-expressing cells activates JAK2 which enhances apolipoprotein interactions with ABCA1 and lipid removal from cells
12176027 Dominant expression of ABCA1 on basolateral surface of Caco-2 cells stimulated by LXR/RXR ligands
12928428 ABCA1-mediated vesicle release involves lipid raft plasma membrane domains
15158913 Both mutations prevent normal trafficking of ABCA1, thereby explaining their inability to mediate apoA1-dependent lipid efflux
16497665 oxidation by myeloperoxidase impairs the ability of apoA-I to promote cholesterol efflux by the ABCA1 pathway, suggesting that this oxidative process might contribute to foam cell formation and atherogenesis
16725228 This study suggest a gender-specific and APOE and UBQLN1 independent association between the ABCA1/R219K polymorphism and late-onset Alzheimer's disease.
17383594 Rare mutations in ABCA1 are associated with low HDL-C. However, at least 1 ABCA1 polymorphism (eg, E1172D) may contribute to the high HDL-C phenotype.
17510466 Interaction of apoA-I with ABCA1 results in the simultaneous generation of pre-beta HDLs of discrete size and chemical composition.
12426219 ABCA1 plays an important role in artery wall cell-mediated modification/oxidation of LDL by modulating the release of reactive oxygen species from artery wall cells that are necessary for LDL oxidation.
12706378 ABCA1 expression varies among tissues, and cholesterol conversion to hydroxycholesterol is an important mechanism for the maintenance of cholesterol homeostasis in fibroblasts
11929608 Apo AI/ABCA1-dependent and HDL3-mediated lipid efflux
12576507 Results describe two new point mutations of the ABCA1 gene found in one patient with Tangier disease and the sibling of another Tangier disease patient.
15033469 ATP-binding-cassette transporter A1 gene expression in macrophages is downregulated by statins
11940086 ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels
15851589 Deficiency of macrophage ACAT1 accelerates atherosclerosis in apoE-/- mice but has no effect when hypercholesterolemia is corrected by apoE expression. ACAT1 deletion impairs ABCA1-mediated cholesterol efflux in macrophages regardless of apoE expression
15890646 cholesterol efflux via the ABCA1/apoA-I pathway is enhanced by the GSL synthesis inhibitor PDMP
16505586 ABCA1 is a rate-limiting factor of HDL assembly and is regulated by transcriptional and post-transcriptional factors. Post-transcriptional regulation of ABCA1 involves modulation of its calpain-mediated degradation.
17196163 The results suggest the promoting effects of AngII on the forming of foam cells are in a dose-dependent manner via down-regulating the expression of ABCA1.
11752403 in the presence of apoE, overexpression of ABCA1 modulates HDL as well as apoB-containing lipoprotein metabolism and reduces atherosclerosis in vivo
14560020 These studies indicate a direct role of retinoic acid receptor gamma/retinoid x receptor in induction of macrophage ABCA1.
16207713 ABCA1 plays a role in the pathogenesis of parenchymal and cerebrovascular amyloid pathology
12511593 ABCA1 is regulated by PEST sequence-mediated calpain proteolysis that appears to be reversed by apolipoprotein-mediated phospholipid efflux
12869555 Phosphorylation of a pest sequence in ABCA1 promotes calpain degradation and is reversed by ApoA-I.
16157450 Based on the results of genome-wide screens, along with biological studies, we selected three genes as candidates for AD risk factors: ATP-binding cassette transporter A1 (ABCA1), cholesterol 25-hydroxylase (CH25H) and cholesterol 24-hydroxylase (CH24H).
16456089 ABCA1 upregulation in macrophages inhibits the progression of atherosclerotic lesions
16825673 ABCA1 is expressed in keratinocytes, where it is negatively regulated by a decrease in cellular cholesterol levels or altered permeability barrier requirements and regulated by activators of LXR, PPARs, and RXR or increases in cellular cholesterol levels
16901265 The role of SREBP-2 in the regulation of ABCA1 transcription via generation of oxysterol ligands for liver X receptor is reported.
17121837 ABCA1 plays a significant role in the regulation of neuronal cholesterol efflux to apolipoprotein E discs.
17241464 Results show that ABCA1 mRNA expression increased in response to dexamethasone in primary rat hepatocytes however, the effect was absent or inhibitory in human HepG2 cells and THP-1 macrophages due to low glucocorticoid receptor levels.
17553166 Our study does not support a major role for the ABCA1 gene as a risk factor for ischaemic stroke
12359250 findings suggest an important role for hepatocyte basolateral membrane ABCA1 in the regulation of the levels of intracellular hepatic cholesterol, as well as plasma HDL
12624133 The K allele was significantly more frequent in FH subjects without premature CHD than in FH subjects with premature CHD suggesting that the genetic variant R219K in ABCA1 could influence the development and progression of atherosclerosis in FH subjects.
14570867 ABCA7 compensates the function of ABCA1 for release of cell cholesterol in a certain condition(s).
12952980 ABCA1 is phosphorylated and stabilized in a pathway in which apoA-I activates PKC alpha by PC-PLC-mediated generation of diacylglycerol
12551894 Golgi is involved in ABCA1-mediated cholesterol efflux.
12600718 Genetic variability of ABCA1 influences development of Alzheimer's disease,possibly by interfering with CNS cholesterol homeostasis.
15721294 type 2 diabetes is associated with ABCA1 gene polymorphisms in a Japanese population
14660648 association of apolipoprotein A-I with lipids reduces its ability to interact with ATP-binding cassette transporter A1(ABCA1) and the lipid translocase activity of ABCA1 generates alpha-LpA-I-like particles
15817453 RhoA has a role in ABCA1-mediated cholesterol efflux
16009332 In this report, a relationship between ApoA-I, DM and ABCA1 has been emphasized.
16443932 Results suggest that ABCA1 transduces signals from apolipoprotein A-I (apoA-I) by complexing and activating Cdc42 and downstream kinases and, therefore, acts as a full apoA-I receptor.
16806540 ABCA1 polymorphisms are associated with varying plasma levels of HDL-C in Pakistani individuals.
15935359 The role of high levels of HDL cholesterol in protection against development of atherosclerosis is generally attributed to its role in reverse cholesterol transport, and the ATP binding cassette transporter A1 is a key element of this process.
17335784 An obvious association between polymorphisms of ABCA1 gene and AD was found; the risk for AD was significantly decreased in K allele (RK+KK genotypes) or KK homozygote carriers compared with RR genotypes carriers.
16873719 generation in vitro of 15 missense mutations that have been described in patients with Tangier disease and familial hypoalphalipoproteinemia. (ABCA1)

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