135 related articles for article (PubMed ID: 18974039)
1. Identification of three loci affecting HDL-cholesterol levels in a screen for chemically induced recessive mutations in mice.
Juan T; Véniant MM; Helmering J; Babij P; Baker DM; Damore MA; Bass MB; Gyuris T; Chhoa M; Li CM; Ebeling C; Amato J; Carlson GA; Lloyd DJ
J Lipid Res; 2009 Mar; 50(3):534-545. PubMed ID: 18974039
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. ABCA1 gene promoter DNA methylation is associated with HDL particle profile and coronary artery disease in familial hypercholesterolemia.
Guay SP; Brisson D; Munger J; Lamarche B; Gaudet D; Bouchard L
Epigenetics; 2012 May; 7(5):464-72. PubMed ID: 22419126
[TBL] [Abstract][Full Text] [Related]
4. Mutations in APOA-I and ABCA1 in Norwegians with low levels of HDL cholesterol.
Berge KE; Leren TP
Clin Chim Acta; 2010 Dec; 411(23-24):2019-23. PubMed ID: 20800056
[TBL] [Abstract][Full Text] [Related]
5. Do DNA sequence variants in ABCA1 contribute to HDL cholesterol levels in the general population?
Pajukanta P
J Clin Invest; 2004 Nov; 114(9):1244-7. PubMed ID: 15520856
[TBL] [Abstract][Full Text] [Related]
6. Identification of novel genetic loci for bone size and mechanosensitivity in an ENU mutant exhibiting decreased bone size.
Srivastava AK; Kapur S; Mohan S; Yu H; Kapur S; Wergedal J; Baylink DJ
J Bone Miner Res; 2005 Jun; 20(6):1041-50. PubMed ID: 15883645
[TBL] [Abstract][Full Text] [Related]
7. Generation of ENU-induced mouse mutants with hypocholesterolemia: novel tools for dissecting plasma lipoprotein homeostasis.
Aigner B; Rathkolb B; Mohr M; Klempt M; Hrabé de Angelis M; Wolf E
Lipids; 2007 Aug; 42(8):731-7. PubMed ID: 17554576
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 15520867
[TBL] [Abstract][Full Text] [Related]
9. 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
Atherosclerosis; 2010 Dec; 213(2):492-8. PubMed ID: 20880529
[TBL] [Abstract][Full Text] [Related]
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
BMC Med Genet; 2009 Jan; 10():1. PubMed ID: 19133158
[TBL] [Abstract][Full Text] [Related]
11. 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
Transl Res; 2007 Apr; 149(4):205-10. PubMed ID: 17383594
[TBL] [Abstract][Full Text] [Related]
12. Plasma levels of 27-hydroxycholesterol in humans and mice with monogenic disturbances of high density lipoprotein metabolism.
Karuna R; Holleboom AG; Motazacker MM; Kuivenhoven JA; Frikke-Schmidt R; Tybjaerg-Hansen A; Georgopoulos S; van Eck M; van Berkel TJ; von Eckardstein A; Rentsch KM
Atherosclerosis; 2011 Feb; 214(2):448-55. PubMed ID: 21130455
[TBL] [Abstract][Full Text] [Related]
13. Hypercholesterolemia in ENU-induced mouse mutants.
Mohr M; Klempt M; Rathkolb B; de Angelis MH; Wolf E; Aigner B
J Lipid Res; 2004 Nov; 45(11):2132-7. PubMed ID: 15342683
[TBL] [Abstract][Full Text] [Related]
14. Genetic determinants of plasma HDL-cholesterol levels in familial hypercholesterolemia.
van Aalst-Cohen ES; Jansen AC; Boekholdt SM; Tanck MW; Fontecha MR; Cheng S; Li J; Defesche JC; Kuivenhoven JA; Kastelein JJ
Eur J Hum Genet; 2005 Oct; 13(10):1137-42. PubMed ID: 16030523
[TBL] [Abstract][Full Text] [Related]
15. 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
Circ Res; 2003 Nov; 93(10):1006-12. PubMed ID: 14576201
[TBL] [Abstract][Full Text] [Related]
16. Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease.
Caruana G; Farlie PG; Hart AH; Bagheri-Fam S; Wallace MJ; Dobbie MS; Gordon CT; Miller KA; Whittle B; Abud HE; Arkell RM; Cole TJ; Harley VR; Smyth IM; Bertram JF
PLoS One; 2013; 8(3):e55429. PubMed ID: 23469164
[TBL] [Abstract][Full Text] [Related]
17. Novel ABCA1 compound variant associated with HDL cholesterol deficiency.
Ho Hong S; Rhyne J; Zeller K; Miller M
Biochim Biophys Acta; 2002 May; 1587(1):60-4. PubMed ID: 12009425
[TBL] [Abstract][Full Text] [Related]
18. Functional annotation of mammalian genomic DNA sequence by chemical mutagenesis: a fine-structure genetic mutation map of a 1- to 2-cM segment of mouse chromosome 7 corresponding to human chromosome 11p14-p15.
Rinchik EM; Carpenter DA; Johnson DK
Proc Natl Acad Sci U S A; 2002 Jan; 99(2):844-9. PubMed ID: 11792855
[TBL] [Abstract][Full Text] [Related]
19. Phenotype-based identification of mouse chromosome instability mutants.
Shima N; Hartford SA; Duffy T; Wilson LA; Schimenti KJ; Schimenti JC
Genetics; 2003 Mar; 163(3):1031-40. PubMed ID: 12663541
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]