(Q28219731)

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Molecular cloning of the human ATP-binding cassette transporter 1 (hABC1): evidence for sterol-dependent regulation in macrophages.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Human ATP-binding cassette transporter 1 (ABC1): genomic organization and identification of the genetic defect in the original Tangier disease kindred

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Complete genomic sequence of the human ABCA1 gene: analysis of the human and mouse ATP-binding cassette A promoter

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

ABC Transporters: From Microorganisms to Man

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Evolution of ATP-binding cassette transporter genes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Membrane topology distinguishes a subfamily of the ATP-binding cassette (ABC) transporters

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Common and rare ABCA1 variants affecting plasma HDL cholesterol

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Mutations in the ABC 1 gene in familial HDL deficiency with defective cholesterol efflux

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Dyslipidemias with desirable plasma total cholesterol levels and angiographically demonstrated coronary artery disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Analysis of hABC1 gene 5' end: additional peptide sequence, promoter region, and four polymorphisms.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Metabolism of apolipoproteins A-I, A-II, and A-IV

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Familial HDL deficiency characterized by hypercatabolism of mature apoA-I but not proapoA-I

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Apolipoprotein A-I deficiency due to a codon 84 nonsense mutation of the apolipoprotein A-I gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Apolipoprotein A-I Q[-2]X causing isolated apolipoprotein A-I deficiency in a family with analphalipoproteinemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

DNA inversion within the apolipoproteins AI/CIII/AIV-encoding gene cluster of certain patients with premature atherosclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Homogeneous assay based on 52 primer sets to scan for mutations of the ABCA1 gene and its application in genetic analysis of a new patient with familial high-density lipoprotein deficiency syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Novel polymorphisms in promoter region of atp binding cassette transporter gene and plasma lipids, severity, progression, and regression of coronary atherosclerosis and response to therapy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5

Familial lipoprotein disorders in patients with premature coronary artery disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900106-5