Common ABCA1 variants, HDL levels, and cellular cholesterol efflux in subjects with familial low HDL. (Q34610302)

3 August 2017

Common ABCA1 variants, HDL levels, and cellular cholesterol efflux in subjects with familial low HDL. (English)

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3 August 2017

3

Miriam Lee-Rueckert

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3 August 2017

9

Matti Jauhiainen

1 reference

3 August 2017

Leena Peltonen-Palotie

10

object named as

Leena Peltonen

1 reference

3 August 2017

Marja-Riitta Taskinen

11

object named as

Marja-Riitta Taskinen

1 reference

3 August 2017

8

Petri T Kovanen

1 reference

3 August 2017

2

Jussi Naukkarinen

1 reference

3 August 2017

Aino Soro-Paavonen

1

1 reference

3 August 2017

Hiroshi Watanabe

4

1 reference

3 August 2017

Elina Rantala

5

1 reference

3 August 2017

Sanni Soderlund

6

1 reference

3 August 2017

Anne Hiukka

7

1 reference

3 August 2017

language of work or name

1 reference

19 March 2007

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Journal of Lipid Research

3 August 2017

8

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published in

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3 August 2017

48

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3 August 2017

1409-1416

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3 August 2017

6

1 reference

Atheroprotective mechanisms of HDL.

3 August 2017

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Regulation of plasma high-density lipoprotein levels by the ABCA1 transporter and the emerging role of high-density lipoprotein in the treatment of cardiovascular disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Intestinal ABCA1 directly contributes to HDL biogenesis in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Monocyte/macrophage expression of ABCA1 has minimal contribution to plasma HDL levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Association between increased arterial-wall thickness and impairment in ABCA1-driven cholesterol efflux: an observational study

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

ABCA1(Alabama): a novel variant associated with HDL deficiency and premature coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Genetic variation in ABC transporter A1 contributes to HDL cholesterol in the general population

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Common variants in the gene encoding ATP-binding cassette transporter 1 in men with low HDL cholesterol levels and coronary heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

ATP-binding cassette transporter A1 locus is not a major determinant of HDL-C levels in a population at high risk for coronary heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

ABCG1 (ABC8), the human homolog of the Drosophila white gene, is a regulator of macrophage cholesterol and phospholipid transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

ATP-binding cassette transporters G1 and G4 mediate cellular cholesterol efflux to high-density lipoproteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Expression and regulation of multiple murine ATP-binding cassette transporter G1 mRNAs/isoforms that stimulate cellular cholesterol efflux to high density lipoprotein

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

ABCG1 redistributes cell cholesterol to domains removable by high density lipoprotein but not by lipid-depleted apolipoproteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Determinants of low HDL levels in familial combined hyperlipidemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Human plasma phospholipid transfer protein increases the antiatherogenic potential of high density lipoproteins in transgenic mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Hypertriglyceridemia is associated with prebeta-HDL concentrations in subjects with familial low HDL.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Decreased high-density lipoprotein (HDL) particle size, prebeta-, and large HDL subspecies concentration in Finnish low-HDL families: relationship with intima-media thickness

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

A system for specific, high-throughput genotyping by allele-specific primer extension on microarrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Chymase in exocytosed rat mast cell granules effectively proteolyzes apolipoprotein AI-containing lipoproteins, so reducing the cholesterol efflux-inducing ability of serum and aortic intimal fluid

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Carotid artery intima-media thickness in Finnish families with familial combined hyperlipidemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

PPAR-alpha and PPAR-gamma activators induce cholesterol removal from human macrophage foam cells through stimulation of the ABCA1 pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Liver X receptor activation controls intracellular cholesterol trafficking and esterification in human macrophages

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Assembly of high density lipoprotein by the ABCA1/apolipoprotein pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Transcriptional regulatory networks in lipid metabolism control ABCA1 expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Relation of lipoprotein subclasses as measured by proton nuclear magnetic resonance spectroscopy to coronary artery disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

ABCG1 has a critical role in mediating cholesterol efflux to HDL and preventing cellular lipid accumulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Characterization of the human ABCG1 gene: liver X receptor activates an internal promoter that produces a novel transcript encoding an alternative form of the protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Expression of the ATP-binding cassette transporter gene ABCG1 (ABC8) in Tangier disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

In-depth haplotype analysis of ABCA1 gene polymorphisms in relation to plasma ApoA1 levels and myocardial infarction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

Targeted inactivation of hepatic Abca1 causes profound hypoalphalipoproteinemia and kidney hypercatabolism of apoA-I

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P600012-JLR200

10.1194/JLR.P600012-JLR200

21 January 2018

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DOI

1 reference

3 August 2017

1 reference