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Items: 1 to 20 of 112

1.

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

Lawn RM, Wade DP, Garvin MR, Wang X, Schwartz K, Porter JG, Seilhamer JJ, Vaughan AM, Oram JF.

J Clin Invest. 1999 Oct;104(8):R25-31.

2.

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

Remaley AT, Rust S, Rosier M, Knapper C, Naudin L, Broccardo C, Peterson KM, Koch C, Arnould I, Prades C, Duverger N, Funke H, Assman G, Dinger M, Dean M, Chimini G, Santamarina-Fojo S, Fredrickson DS, Denefle P, Brewer HB Jr.

Proc Natl Acad Sci U S A. 1999 Oct 26;96(22):12685-90.

3.

Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux.

Marcil M, Brooks-Wilson A, Clee SM, Roomp K, Zhang LH, Yu L, Collins JA, van Dam M, Molhuizen HO, Loubster O, Ouellette BF, Sensen CW, Fichter K, Mott S, Denis M, Boucher B, Pimstone S, Genest J Jr, Kastelein JJ, Hayden MR.

Lancet. 1999 Oct 16;354(9187):1341-6.

PMID:
10533863
4.

Transport of lipids from golgi to plasma membrane is defective in tangier disease patients and Abc1-deficient mice.

Orsó E, Broccardo C, Kaminski WE, Böttcher A, Liebisch G, Drobnik W, Götz A, Chambenoit O, Diederich W, Langmann T, Spruss T, Luciani MF, Rothe G, Lackner KJ, Chimini G, Schmitz G.

Nat Genet. 2000 Feb;24(2):192-6.

PMID:
10655069
5.
6.

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

Bodzioch M, Orsó E, Klucken J, Langmann T, Böttcher A, Diederich W, Drobnik W, Barlage S, Büchler C, Porsch-Ozcürümez M, Kaminski WE, Hahmann HW, Oette K, Rothe G, Aslanidis C, Lackner KJ, Schmitz G.

Nat Genet. 1999 Aug;22(4):347-51.

PMID:
10431237
7.

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

Rust S, Rosier M, Funke H, Real J, Amoura Z, Piette JC, Deleuze JF, Brewer HB, Duverger N, Denèfle P, Assmann G.

Nat Genet. 1999 Aug;22(4):352-5.

PMID:
10431238
8.

ABC1: connecting yellow tonsils, neuropathy, and very low HDL.

Hobbs HH, Rader DJ.

J Clin Invest. 1999 Oct;104(8):1015-7. No abstract available.

9.

High density lipoprotein deficiency and foam cell accumulation in mice with targeted disruption of ATP-binding cassette transporter-1.

McNeish J, Aiello RJ, Guyot D, Turi T, Gabel C, Aldinger C, Hoppe KL, Roach ML, Royer LJ, de Wet J, Broccardo C, Chimini G, Francone OL.

Proc Natl Acad Sci U S A. 2000 Apr 11;97(8):4245-50.

10.

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

Brooks-Wilson A, Marcil M, Clee SM, Zhang LH, Roomp K, van Dam M, Yu L, Brewer C, Collins JA, Molhuizen HO, Loubser O, Ouelette BF, Fichter K, Ashbourne-Excoffon KJ, Sensen CW, Scherer S, Mott S, Denis M, Martindale D, Frohlich J, Morgan K, Koop B, Pimstone S, Kastelein JJ, Genest J Jr, Hayden MR.

Nat Genet. 1999 Aug;22(4):336-45.

PMID:
10431236
11.

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

Mott S, Yu L, Marcil M, Boucher B, Rondeau C, Genest J Jr.

Atherosclerosis. 2000 Oct;152(2):457-68.

PMID:
10998475
12.
13.

ABC1: the gene for Tangier disease and beyond.

Ordovas JM.

Nutr Rev. 2000 Mar;58(3 Pt 1):76-9. Review.

PMID:
10812922
14.

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

Remaley AT, Schumacher UK, Stonik JA, Farsi BD, Nazih H, Brewer HB Jr.

Arterioscler Thromb Vasc Biol. 1997 Sep;17(9):1813-21.

15.

Scavenger receptor-BI inhibits ATP-binding cassette transporter 1- mediated cholesterol efflux in macrophages.

Chen W, Silver DL, Smith JD, Tall AR.

J Biol Chem. 2000 Oct 6;275(40):30794-800.

16.

A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.

Bertolini S, Pisciotta L, Seri M, Cusano R, Cantafora A, Calabresi L, Franceschini G, Ravazzolo R, Calandra S.

Atherosclerosis. 2001 Feb 15;154(3):599-605.

PMID:
11257260
17.

ABCA1-mediated transport of cellular cholesterol and phospholipids to HDL apolipoproteins.

Oram JF, Vaughan AM.

Curr Opin Lipidol. 2000 Jun;11(3):253-60. Review.

PMID:
10882340
18.

Tangier disease and ABCA1.

Oram JF.

Biochim Biophys Acta. 2000 Dec 15;1529(1-3):321-30. Review.

PMID:
11111099
19.

ABC1 gene expression and ApoA-I-mediated cholesterol efflux are regulated by LXR.

Schwartz K, Lawn RM, Wade DP.

Biochem Biophys Res Commun. 2000 Aug 11;274(3):794-802.

PMID:
10924356

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