206 related articles for article (PubMed ID: 10535983)
21. A novel ABCA1 nonsense mutation, R1270X, in Tangier disease associated with an unrecognised bleeding tendency.
Hooper AJ; Robertson K; Ng L; Kattampallil JS; Latchem D; Willsher PC; Thom J; Baker RI; Burnett JR
Clin Chim Acta; 2009 Nov; 409(1-2):136-9. PubMed ID: 19723515
[TBL] [Abstract][Full Text] [Related]
22. The correlation of ATP-binding cassette 1 mRNA levels with cholesterol efflux from various cell lines.
Bortnick AE; Rothblat GH; Stoudt G; Hoppe KL; Royer LJ; McNeish J; Francone OL
J Biol Chem; 2000 Sep; 275(37):28634-40. PubMed ID: 10893411
[TBL] [Abstract][Full Text] [Related]
23. Tangier disease caused by compound heterozygosity for ABCA1 mutations R282X and Y1532C.
Cameron J; Ranheim T; Halvorsen B; Kulseth MA; Leren TP; Berge KE
Atherosclerosis; 2010 Mar; 209(1):163-6. PubMed ID: 19765707
[TBL] [Abstract][Full Text] [Related]
24. Novel mutations in the gene encoding ATP-binding cassette 1 in four tangier disease kindreds.
Brousseau ME; Schaefer EJ; Dupuis J; Eustace B; Van Eerdewegh P; Goldkamp AL; Thurston LM; FitzGerald MG; Yasek-McKenna D; O'Neill G; Eberhart GP; Weiffenbach B; Ordovas JM; Freeman MW; Brown RH; Gu JZ
J Lipid Res; 2000 Mar; 41(3):433-41. PubMed ID: 10706591
[TBL] [Abstract][Full Text] [Related]
25. Cholesterol efflux regulatory protein, Tangier disease and familial high-density lipoprotein deficiency.
Hayden MR; Clee SM; Brooks-Wilson A; Genest J; Attie A; Kastelein JJ
Curr Opin Lipidol; 2000 Apr; 11(2):117-22. PubMed ID: 10787172
[TBL] [Abstract][Full Text] [Related]
26. 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; 271(2):451-5. PubMed ID: 10799318
[TBL] [Abstract][Full Text] [Related]
27. Common and rare ABCA1 variants affecting plasma HDL cholesterol.
Wang J; Burnett JR; Near S; Young K; Zinman B; Hanley AJ; Connelly PW; Harris SB; Hegele RA
Arterioscler Thromb Vasc Biol; 2000 Aug; 20(8):1983-9. PubMed ID: 10938021
[TBL] [Abstract][Full Text] [Related]
28. Identification and characterization of a mammalian mitochondrial ATP-binding cassette membrane protein.
Hogue DL; Liu L; Ling V
J Mol Biol; 1999 Jan; 285(1):379-89. PubMed ID: 9878413
[TBL] [Abstract][Full Text] [Related]
29. Expression of the ATP-binding cassette transporter gene ABCG1 (ABC8) in Tangier disease.
Lorkowski S; Kratz M; Wenner C; Schmidt R; Weitkamp B; Fobker M; Reinhardt J; Rauterberg J; Galinski EA; Cullen P
Biochem Biophys Res Commun; 2001 May; 283(4):821-30. PubMed ID: 11350058
[TBL] [Abstract][Full Text] [Related]
30. A case of Tangier disease with a novel mutation in the C-terminal region of ATP-binding cassette transporter A1.
Guan JZ; Tamasawa N; Brunham LR; Matsui J; Murakami H; Suda T; Ochiai S; Tsutsui M; Kudou K; Satoh K; Hayden MR
Am J Med Genet A; 2004 Nov; 130A(4):398-401. PubMed ID: 15384103
[TBL] [Abstract][Full Text] [Related]
31. A novel mutation in the ABCA1 gene causing an atypical phenotype of Tangier disease.
Negi SI; Brautbar A; Virani SS; Anand A; Polisecki E; Asztalos BF; Ballantyne CM; Schaefer EJ; Jones PH
J Clin Lipidol; 2013; 7(1):82-7. PubMed ID: 23351586
[TBL] [Abstract][Full Text] [Related]
32. Screening for functional sequence variations and mutations in ABCA1.
Probst MC; Thumann H; Aslanidis C; Langmann T; Buechler C; Patsch W; Baralle FE; Dallinga-Thie GM; Geisel J; Keller C; Menys VC; Schmitz G
Atherosclerosis; 2004 Aug; 175(2):269-79. PubMed ID: 15262183
[TBL] [Abstract][Full Text] [Related]
33. Identification of the first Tangier disease patient in Lebanon carrying a new pathogenic variant in ABCA1.
El Khoury P; Couvert P; Elbitar S; Ghaleb Y; Abou-Khalil Y; Azar Y; Ayoub C; Superville A; Guérin M; Rabès JP; Varret M; Boileau C; Jambart S; Giral P; Carrié A; Le Goff W; Abifadel M
J Clin Lipidol; 2018; 12(6):1374-1382. PubMed ID: 30361172
[TBL] [Abstract][Full Text] [Related]
34. Gene linked to faulty cholesterol transport.
Gura T
Science; 1999 Aug; 285(5429):814-5. PubMed ID: 10454927
[No Abstract] [Full Text] [Related]
35. A, B, C...gamma!
Tall AR; Schindler CW
Arterioscler Thromb Vasc Biol; 2000 Jun; 20(6):1423-4. PubMed ID: 10845853
[No Abstract] [Full Text] [Related]
36. Promoter haplotype of a new ABCA1 mutant influences expression of familial hypoalphalipoproteinemia.
Slatter TL; Williams MJ; Frikke-Schmidt R; Tybjaerg-Hansen A; Morison IM; McCormick SP
Atherosclerosis; 2006 Aug; 187(2):393-400. PubMed ID: 16225879
[TBL] [Abstract][Full Text] [Related]
37. An ATP-driven efflux pump is a novel pathogenicity factor in rice blast disease.
Urban M; Bhargava T; Hamer JE
EMBO J; 1999 Feb; 18(3):512-21. PubMed ID: 9927411
[TBL] [Abstract][Full Text] [Related]
38. Tangier disease: epidemiology, pathophysiology, and management.
Puntoni M; Sbrana F; Bigazzi F; Sampietro T
Am J Cardiovasc Drugs; 2012 Oct; 12(5):303-11. PubMed ID: 22913675
[TBL] [Abstract][Full Text] [Related]
39. A novel missense mutation of ABCA1 in transmembrane alpha-helix in a Japanese patient with Tangier disease.
Maekawa M; Kikuchi J; Kotani K; Nagao K; Odgerel T; Ueda K; Kawano M; Furukawa Y; Sakurabayashi I
Atherosclerosis; 2009 Sep; 206(1):216-22. PubMed ID: 19344898
[TBL] [Abstract][Full Text] [Related]
40. Severe Tangier disease with a novel ABCA1 gene mutation.
Schippling S; Orth M; Beisiegel U; Rosenkranz T; Vogel P; Münchau A; Hagel C; Seedorf U
Neurology; 2008 Oct; 71(18):1454-5. PubMed ID: 18955690
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]