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Items: 1 to 20 of 78

1.

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

Pullinger CR, Hakamata H, Duchateau PN, Eng C, Aouizerat BE, Cho MH, Fielding CJ, Kane JP.

Biochem Biophys Res Commun. 2000 May 10;271(2):451-5.

PMID:
10799318
2.

Sterol-dependent transactivation of the ABC1 promoter by the liver X receptor/retinoid X receptor.

Costet P, Luo Y, Wang N, Tall AR.

J Biol Chem. 2000 Sep 8;275(36):28240-5.

3.

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
4.

Polymorphisms of the porcine androgen receptor gene affecting its amino acid sequence and expression level.

Trakooljul N, Ponsuksili S, Schellander K, Wimmers K.

Biochim Biophys Acta. 2004 May 25;1678(2-3):94-101.

PMID:
15157735
5.

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

Langmann T, Klucken J, Reil M, Liebisch G, Luciani MF, Chimini G, Kaminski WE, Schmitz G.

Biochem Biophys Res Commun. 1999 Apr 2;257(1):29-33.

PMID:
10092505
6.

Identification of sterol-independent regulatory elements in the human ATP-binding cassette transporter A1 promoter: role of Sp1/3, E-box binding factors, and an oncostatin M-responsive element.

Langmann T, Porsch-Ozcürümez M, Heimerl S, Probst M, Moehle C, Taher M, Borsukova H, Kielar D, Kaminski WE, Dittrich-Wengenroth E, Schmitz G.

J Biol Chem. 2002 Apr 26;277(17):14443-50. Epub 2002 Feb 11.

7.

Genomic sequence and structure of the human ABCG1 (ABC8) gene.

Lorkowski S, Rust S, Engel T, Jung E, Tegelkamp K, Galinski EA, Assmann G, Cullen P.

Biochem Biophys Res Commun. 2001 Jan 12;280(1):121-31.

PMID:
11162488
9.

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
10.

Genetic variation in ABC transporter A1 contributes to HDL cholesterol in the general population.

Frikke-Schmidt R, Nordestgaard BG, Jensen GB, Tybjaerg-Hansen A.

J Clin Invest. 2004 Nov;114(9):1343-53.

11.

Characterization of the infection-responsive bovine lactoferrin promoter.

Zheng J, Ather JL, Sonstegard TS, Kerr DE.

Gene. 2005 Jun 20;353(1):107-17.

PMID:
15935571
12.

Analysis of mono-ADP-ribosyltransferase 4 gene expression in human monocytes: splicing pattern and potential regulatory elements.

Grahnert A, Friedrich M, Engeland K, Hauschildt S.

Biochim Biophys Acta. 2005 Sep 25;1730(3):173-86.

PMID:
16140404
13.

Genomic organization and characterization of the promoter of the human ATP-binding cassette transporter-G1 (ABCG1) gene.

Langmann T, Porsch-Ozcürümez M, Unkelbach U, Klucken J, Schmitz G.

Biochim Biophys Acta. 2000 Nov 15;1494(1-2):175-80.

PMID:
11072082
14.

Complete coding sequence, promoter region, and genomic structure of the human ABCA2 gene and evidence for sterol-dependent regulation in macrophages.

Kaminski WE, Piehler A, Püllmann K, Porsch-Ozcürümez M, Duong C, Bared GM, Büchler C, Schmitz G.

Biochem Biophys Res Commun. 2001 Feb 16;281(1):249-58.

PMID:
11178988
15.

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

Santamarina-Fojo S, Peterson K, Knapper C, Qiu Y, Freeman L, Cheng JF, Osorio J, Remaley A, Yang XP, Haudenschild C, Prades C, Chimini G, Blackmon E, Francois T, Duverger N, Rubin EM, Rosier M, Denèfle P, Fredrickson DS, Brewer HB Jr.

Proc Natl Acad Sci U S A. 2000 Jul 5;97(14):7987-92. Erratum in: Proc Natl Acad Sci U S A 2002 Jan 22;99(2):1098.

16.

Mouse vesicular GABA transporter gene: genomic organization, transcriptional regulation and chromosomal localization.

Ebihara S, Obata K, Yanagawa Y.

Brain Res Mol Brain Res. 2003 Jan 31;110(1):126-39.

PMID:
12573541
17.

A promoter variant of the ATP-binding cassette transporter A1 gene alters the HDL cholesterol level in the general Japanese population.

Shioji K, Nishioka J, Naraba H, Kokubo Y, Mannami T, Inamoto N, Kamide K, Takiuchi S, Yoshii M, Miwa Y, Kawano Y, Miyata T, Miyazaki S, Goto Y, Nonogi H, Tago N, Iwai N.

J Hum Genet. 2004;49(3):141-7. Epub 2004 Feb 21.

PMID:
14986172
18.

Eight novel ABCD1 gene mutations and three polymorphisms in patients with X-linked adrenoleukodystrophy: The first polymorphism causing an amino acid exchange.

Dvoráková L, Storkánová G, Unterrainer G, Hujová J, Kmoch S, Zeman J, Hrebícek M, Berger J.

Hum Mutat. 2001;18(1):52-60.

PMID:
11438993
19.

Cloning, characterisation and identification of several polymorphisms in the promoter region of the human alpha2B-adrenergic receptor gene.

Cayla C, Heinonen P, Viikari L, Schaak S, Snapir A, Bouloumié A, Karvonen MK, Pesonen U, Scheinin M, Paris H.

Biochem Pharmacol. 2004 Feb 1;67(3):469-78.

PMID:
15037199
20.

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.

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