Similar articles for PMID: 12009425

Year	Number of Results
1994	1
1998	1
1999	3
2000	4
2001	4
2002	5
2003	5
2004	4
2005	7
2006	8
2007	6
2008	7
2009	9
2010	8
2011	6
2012	5
2013	1
2014	1
2015	2
2018	2
2019	1
2022	1
2023	1
2024	0

1

Novel ABCA1 compound variant associated with HDL cholesterol deficiency.

Ho Hong S, Rhyne J, Zeller K, Miller M. Ho Hong S, et al. Biochim Biophys Acta. 2002 May 21;1587(1):60-4. doi: 10.1016/s0925-4439(02)00066-2. Biochim Biophys Acta. 2002. PMID: 12009425 Free article.

2

ABCA1(Alabama): a novel variant associated with HDL deficiency and premature coronary artery disease.

Hong SH, Rhyne J, Zeller K, Miller M. Hong SH, et al. Atherosclerosis. 2002 Oct;164(2):245-50. doi: 10.1016/s0021-9150(02)00106-5. Atherosclerosis. 2002. PMID: 12204794 Review.

3

Novel polypyrimidine variation (IVS46: del T -39...-46) in ABCA1 causes exon skipping and contributes to HDL cholesterol deficiency in a family with premature coronary disease.

Hong SH, Rhyne J, Miller M. Hong SH, et al. Circ Res. 2003 Nov 14;93(10):1006-12. doi: 10.1161/01.RES.0000102957.84247.8F. Epub 2003 Oct 23. Circ Res. 2003. PMID: 14576201

4

Lack of association between increased carotid intima-media thickening and decreased HDL-cholesterol in a family with a novel ABCA1 variant, G2265T.

Hong SH, Riley W, Rhyne J, Friel G, Miller M. Hong SH, et al. Clin Chem. 2002 Nov;48(11):2066-70. Clin Chem. 2002. PMID: 12407001

5

Genotypic variation in ATP-binding cassette transporter-1 (ABCA1) as contributors to the high and low high-density lipoprotein-cholesterol (HDL-C) phenotype.

Mantaring M, Rhyne J, Ho Hong S, Miller M. Mantaring M, et al. Transl Res. 2007 Apr;149(4):205-10. doi: 10.1016/j.trsl.2006.11.007. Transl Res. 2007. PMID: 17383594

6

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. Mott S, et al. Atherosclerosis. 2000 Oct;152(2):457-68. doi: 10.1016/s0021-9150(99)00498-0. Atherosclerosis. 2000. PMID: 10998475

7

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. Marcil M, et al. Lancet. 1999 Oct 16;354(9187):1341-6. doi: 10.1016/s0140-6736(99)07026-9. Lancet. 1999. PMID: 10533863

8

Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol.

Candini C, Schimmel AW, Peter J, Bochem AE, Holleboom AG, Vergeer M, Dullaart RP, Dallinga-Thie GM, Hovingh GK, Khoo KL, Fasano T, Bocchi L, Calandra S, Kuivenhoven JA, Motazacker MM. Candini C, et al. Atherosclerosis. 2010 Dec;213(2):492-8. doi: 10.1016/j.atherosclerosis.2010.08.062. Epub 2010 Aug 26. Atherosclerosis. 2010. PMID: 20880529

9

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. Wang J, et al. Arterioscler Thromb Vasc Biol. 2000 Aug;20(8):1983-9. doi: 10.1161/01.atv.20.8.1983. Arterioscler Thromb Vasc Biol. 2000. PMID: 10938021

10

Multiple splice defects in ABCA1 cause low HDL-C in a family with hypoalphalipoproteinemia and premature coronary disease.

Rhyne J, Mantaring MM, Gardner DF, Miller M. Rhyne J, et al. BMC Med Genet. 2009 Jan 8;10:1. doi: 10.1186/1471-2350-10-1. BMC Med Genet. 2009. PMID: 19133158 Free PMC article.

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