Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations (Q74348218)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998475%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998475%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

main subject

hypoalphalipoproteinemia

1 reference

S Mott

1

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10 November 2019

L Yu

2

1 reference

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10 November 2019

M Marcil

3

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10 November 2019

B Boucher

4

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10 November 2019

C Rondeau

5

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10 November 2019

J Genest

6

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10 November 2019

publication date

1 October 2000

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10 November 2019

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10 November 2019

volume

152

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10 November 2019

issue

2

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10 November 2019

page(s)

457-468

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High density lipoproteins and coronary heart disease

10 November 2019

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In vivo metabolism of a mutant form of apolipoprotein A-I, apo A-IMilano, associated with familial hypoalphalipoproteinemia

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High density lipoprotein and coronary heart disease: insights from mutations leading to low high density lipoprotein

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The high density lipoprotein- and apolipoprotein A-I-induced mobilization of cellular cholesterol is impaired in fibroblasts from Tangier disease subjects

7 January 2021

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Defective removal of cellular cholesterol and phospholipids by apolipoprotein A-I in Tangier Disease

7 January 2021

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HDL-mediated efflux of intracellular cholesterol is impaired in fibroblasts from Tangier disease patients

7 January 2021

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Decreased reverse cholesterol transport from Tangier disease fibroblasts. Acceptor specificity and effect of brefeldin on lipid efflux

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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Cellular cholesterol transport and efflux in fibroblasts are abnormal in subjects with familial HDL deficiency

7 January 2021

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7 January 2021

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7 January 2021

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The effect of high density lipoprotein phospholipid acyl chain composition on the efflux of cellular free cholesterol.

7 January 2021

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Protein kinase C-alpha levels are inversely associated with growth rate in cultured human dermal fibroblasts

7 January 2021

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7 January 2021

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Defective regulation of phosphatidylcholine-specific phospholipases C and D in a kindred with Tangier disease. Evidence for the involvement of phosphatidylcholine breakdown in HDL-mediated cholesterol efflux mechanisms

7 January 2021

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7 January 2021

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7 January 2021

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10.1016/S0021-9150(99)00498-0

7 January 2021

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998475%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

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