(Q43992175)

28 November 2017

title

Novel ABCA1 compound variant associated with HDL cholesterol deficiency (English)

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28 November 2017

Seung Ho Hong

1

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28 November 2017

Jeffrey Rhyne

series ordinal

2

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28 November 2017

Karen Zeller

series ordinal

3

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28 November 2017

Michael Miller

series ordinal

4

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28 November 2017

publication date

1 May 2002

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Biochimica et Biophysica Acta

28 November 2017

published in

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28 November 2017

volume

1587

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28 November 2017

issue

1

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28 November 2017

page(s)

60-64

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ABC Transporters: From Microorganisms to Man

28 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

Evolution of ATP-binding cassette transporter genes

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7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

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https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

Common and rare ABCA1 variants affecting plasma HDL cholesterol

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900066-2

7 January 2021

10.1016/S0925-4439(02)00066-2

Identifiers

DOI

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28 November 2017

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