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Results: 1 to 20 of 101

Similar articles for PubMed (Select 19553242)

1.

Identification of a novel human cellular HDL biosynthesis defect.

Rashid S, Marcil M, Ruel I, Genest J.

Eur Heart J. 2009 Sep;30(18):2204-12. doi: 10.1093/eurheartj/ehp250. Epub 2009 Jun 24.

2.

Cellular phospholipid and cholesterol efflux in high-density lipoprotein deficiency.

Marcil M, Bissonnette R, Vincent J, Krimbou L, Genest J.

Circulation. 2003 Mar 18;107(10):1366-71.

3.

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
4.

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
5.

Cellular cholesterol efflux in heterozygotes for tangier disease is markedly reduced and correlates with high density lipoprotein cholesterol concentration and particle size.

Brousseau ME, Eberhart GP, Dupuis J, Asztalos BF, Goldkamp AL, Schaefer EJ, Freeman MW.

J Lipid Res. 2000 Jul;41(7):1125-35.

6.

Impaired ABCA1-dependent lipid efflux and hypoalphalipoproteinemia in human Niemann-Pick type C disease.

Choi HY, Karten B, Chan T, Vance JE, Greer WL, Heidenreich RA, Garver WS, Francis GA.

J Biol Chem. 2003 Aug 29;278(35):32569-77. Epub 2003 Jun 16.

7.

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.

8.

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

Marcil M, Yu L, Krimbou L, Boucher B, Oram JF, Cohn JS, Genest J Jr.

Arterioscler Thromb Vasc Biol. 1999 Jan;19(1):159-69.

9.

Genetic etiology of isolated low HDL syndrome: incidence and heterogeneity of efflux defects.

Kiss RS, Kavaslar N, Okuhira K, Freeman MW, Walter S, Milne RW, McPherson R, Marcel YL.

Arterioscler Thromb Vasc Biol. 2007 May;27(5):1139-45. Epub 2007 Feb 15.

10.

Expression and functional analyses of novel mutations of ATP-binding cassette transporter-1 in Japanese patients with high-density lipoprotein deficiency.

Nishida Y, Hirano K, Tsukamoto K, Nagano M, Ikegami C, Roomp K, Ishihara M, Sakane N, Zhang Z, Tsujii Ki K, Matsuyama A, Ohama T, Matsuura F, Ishigami M, Sakai N, Hiraoka H, Hattori H, Wellington C, Yoshida Y, Misugi S, Hayden MR, Egashira T, Yamashita S, Matsuzawa Y.

Biochem Biophys Res Commun. 2002 Jan 18;290(2):713-21.

PMID:
11785958
11.

Common ABCA1 variants, HDL levels, and cellular cholesterol efflux in subjects with familial low HDL.

Soro-Paavonen A, Naukkarinen J, Lee-Rueckert M, Watanabe H, Rantala E, Soderlund S, Hiukka A, Kovanen PT, Jauhiainen M, Peltonen L, Taskinen MR.

J Lipid Res. 2007 Jun;48(6):1409-16. Epub 2007 Mar 19.

12.

cAMP induces ABCA1 phosphorylation activity and promotes cholesterol efflux from fibroblasts.

Haidar B, Denis M, Krimbou L, Marcil M, Genest J Jr.

J Lipid Res. 2002 Dec;43(12):2087-94.

13.

Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency.

Fasano T, Zanoni P, Rabacchi C, Pisciotta L, Favari E, Adorni MP, Deegan PB, Park A, Hlaing T, Feher MD, Jones B, Uzak AS, Kardas F, Dardis A, Sechi A, Bembi B, Minuz P, Bertolini S, Bernini F, Calandra S.

Mol Genet Metab. 2012 Nov;107(3):534-41. doi: 10.1016/j.ymgme.2012.08.005. Epub 2012 Aug 18.

PMID:
22959828
14.

The role of the ABCA1 transporter and cholesterol efflux in familial hypoalphalipoproteinemia.

Hovingh GK, Van Wijland MJ, Brownlie A, Bisoendial RJ, Hayden MR, Kastelein JJ, Groen AK.

J Lipid Res. 2003 Jun;44(6):1251-5. Epub 2003 Apr 16.

15.

Functional mutations of the ABCA1 gene in subjects of French-Canadian descent with HDL deficiency.

Alrasadi K, Ruel IL, Marcil M, Genest J.

Atherosclerosis. 2006 Oct;188(2):281-91. Epub 2005 Dec 15.

PMID:
16343503
16.

Association of HDL deficiency with a novel mutation in the ABCA1 gene.

Denk GU, Aslanidis C, Schmitz G, Parhofer KG, Pusl T.

Exp Clin Endocrinol Diabetes. 2011 Jan;119(1):53-5. doi: 10.1055/s-0030-1254138. Epub 2010 Jun 8.

PMID:
20533173
17.
18.

Correction of apolipoprotein A-I-mediated lipid efflux and high density lipoprotein particle formation in human Niemann-Pick type C disease fibroblasts.

Boadu E, Choi HY, Lee DW, Waddington EI, Chan T, Asztalos B, Vance JE, Chan A, Castro G, Francis GA.

J Biol Chem. 2006 Dec 1;281(48):37081-90. Epub 2006 Oct 3.

19.

Accumulation of cardiolipin and lysocardiolipin in fibroblasts from Tangier disease subjects.

Fobker M, Voss R, Reinecke H, Crone C, Assmann G, Walter M.

FEBS Lett. 2001 Jul 6;500(3):157-62.

20.

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
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