(Q36979012)

17 August 2017

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title

Cholesterol fill-in model: mechanism for substrate recognition by ABC proteins (English)

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17 August 2017

Yasuhisa Kimura

1

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17 August 2017

Atsushi Kodan

series ordinal

2

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17 August 2017

Michinori Matsuo

series ordinal

3

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17 August 2017

Kazumitsu Ueda

series ordinal

4

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17 August 2017

publication date

1 December 2007

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Journal of Bioenergetics and Biomembranes

17 August 2017

published in

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17 August 2017

volume

39

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17 August 2017

issue

5-6

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17 August 2017

page(s)

447-452

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ATP-binding cassette transporter A1 (ABCA1) functions as a cholesterol efflux regulatory protein

17 August 2017

cites work

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12 December 2020

A two-step mechanism for free cholesterol and phospholipid efflux from human vascular cells to apolipoprotein A-1.

1 reference

12 December 2020

Alteration of Substrate Specificity by Mutations at the His61Position in Predicted Transmembrane Domain 1 of Human MDR1/P-Glycoprotein†

1 reference

12 December 2020

Increased lipid rafts and accelerated lipopolysaccharide-induced tumor necrosis factor-α secretion in Abca1-deficient macrophages

1 reference

12 December 2020

Naturally occurring mutations in the largest extracellular loops of ABCA1 can disrupt its direct interaction with apolipoprotein A-I

1 reference

12 December 2020

MDR3 P-glycoprotein, a phosphatidylcholine translocase, transports several cytotoxic drugs and directly interacts with drugs as judged by interference with nucleotide trapping

1 reference

12 December 2020

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

1 reference

12 December 2020

Purification and ATPase activity of human ABCA1.

1 reference

12 December 2020

Enhanced apoA-I-dependent cholesterol efflux by ABCA1 from sphingomyelin-deficient Chinese hamster ovary cells

1 reference

12 December 2020

Sequence of mdr3 cDNA encoding a human P-glycoprotein

1 reference

12 December 2020

Aureobasidin A, an antifungal cyclic depsipeptide antibiotic, is a substrate for both human MDR1 and MDR2/P-glycoproteins

1 reference

12 December 2020

Phosphatidylcholine translocase: a physiological role for the mdr2 gene

1 reference

12 December 2020

Efflux of sphingomyelin, cholesterol, and phosphatidylcholine by ABCG1

1 reference

12 December 2020

ATP-binding cassette transporter A7 (ABCA7) binds apolipoprotein A-I and mediates cellular phospholipid but not cholesterol efflux

1 reference

12 December 2020

Molecular machinery for non-vesicular trafficking of ceramide

1 reference

12 December 2020

Bile salt-dependent efflux of cellular phospholipids mediated by ATP binding cassette protein B4

1 reference

12 December 2020

Effects of mutations of ABCA1 in the first extracellular domain on subcellular trafficking and ATP binding/hydrolysis

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Modulation of drug-stimulated ATPase activity of human MDR1/P-glycoprotein by cholesterol

1 reference

12 December 2020

Sphingomyelin-dependence of cholesterol efflux mediated by ABCG1.

1 reference

12 December 2020

Specific binding of ApoA-I, enhanced cholesterol efflux, and altered plasma membrane morphology in cells expressing ABC1.

1 reference

12 December 2020

ATP-binding cassette transporter A1 expression disrupts raft membrane microdomains through its ATPase-related functions.

1 reference

12 December 2020

Sterol transfer by ABCG5 and ABCG8: in vitro assay and reconstitution

1 reference

12 December 2020

Amino acid substitutions in the first transmembrane domain (TM1) of P-glycoprotein that alter substrate specificity

1 reference

12 December 2020

Expression of a full-length cDNA for the human "MDR1" gene confers resistance to colchicine, doxorubicin, and vinblastine

1 reference

12 December 2020

Heterogeneity of high density lipoprotein generated by ABCA1 and ABCA7.

1 reference

12 December 2020

Human ABCA1 contains a large amino-terminal extracellular domain homologous to an epitope of Sjögren's Syndrome

1 reference

12 December 2020

10.1007/S10863-007-9109-7

Identifiers

DOI

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17 August 2017

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