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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2003 | 1 |
2008 | 1 |
2009 | 2 |
2010 | 1 |
2024 | 0 |
PubMed for id: 12360
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SF4 and SFRS14, two related putative splicing factors on human chromosome 19p13.11.
Gene. 2003 Feb 13;305(1):91-100. doi: 10.1016/s0378-1119(02)01230-1.
Gene. 2003.
PMID: 12594045
Large-scale proteomic analysis of the human spliceosome.
Rappsilber J, Ryder U, Lamond AI, Mann M.
Rappsilber J, et al.
Genome Res. 2002 Aug;12(8):1231-45. doi: 10.1101/gr.473902.
Genome Res. 2002.
PMID: 12176931
Free PMC article.
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A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia.
Hegele RA, Ban MR, Hsueh N, Kennedy BA, Cao H, Zou GY, Anand S, Yusuf S, Huff MW, Wang J.
Hegele RA, et al.
Hum Mol Genet. 2009 Nov 1;18(21):4189-94. doi: 10.1093/hmg/ddp361. Epub 2009 Aug 5.
Hum Mol Genet. 2009.
PMID: 19656773
Free PMC article.
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Genetic variants influencing circulating lipid levels and risk of coronary artery disease.
Waterworth DM, Ricketts SL, Song K, Chen L, Zhao JH, Ripatti S, Aulchenko YS, Zhang W, Yuan X, Lim N, Luan J, Ashford S, Wheeler E, Young EH, Hadley D, Thompson JR, Braund PS, Johnson T, Struchalin M, Surakka I, Luben R, Khaw KT, Rodwell SA, Loos RJ, Boekholdt SM, Inouye M, Deloukas P, Elliott P, Schlessinger D, Sanna S, Scuteri A, Jackson A, Mohlke KL, Tuomilehto J, Roberts R, Stewart A, Kesäniemi YA, Mahley RW, Grundy SM; Wellcome Trust Case Control Consortium; McArdle W, Cardon L, Waeber G, Vollenweider P, Chambers JC, Boehnke M, Abecasis GR, Salomaa V, Järvelin MR, Ruokonen A, Barroso I, Epstein SE, Hakonarson HH, Rader DJ, Reilly MP, Witteman JC, Hall AS, Samani NJ, Strachan DP, Barter P, van Duijn CM, Kooner JS, Peltonen L, Wareham NJ, McPherson R, Mooser V, Sandhu MS.
Waterworth DM, et al.
Arterioscler Thromb Vasc Biol. 2010 Nov;30(11):2264-76. doi: 10.1161/ATVBAHA.109.201020. Epub 2010 Sep 23.
Arterioscler Thromb Vasc Biol. 2010.
PMID: 20864672
Free PMC article.
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Common variants at 30 loci contribute to polygenic dyslipidemia.
Kathiresan S, Willer CJ, Peloso GM, Demissie S, Musunuru K, Schadt EE, Kaplan L, Bennett D, Li Y, Tanaka T, Voight BF, Bonnycastle LL, Jackson AU, Crawford G, Surti A, Guiducci C, Burtt NP, Parish S, Clarke R, Zelenika D, Kubalanza KA, Morken MA, Scott LJ, Stringham HM, Galan P, Swift AJ, Kuusisto J, Bergman RN, Sundvall J, Laakso M, Ferrucci L, Scheet P, Sanna S, Uda M, Yang Q, Lunetta KL, Dupuis J, de Bakker PI, O'Donnell CJ, Chambers JC, Kooner JS, Hercberg S, Meneton P, Lakatta EG, Scuteri A, Schlessinger D, Tuomilehto J, Collins FS, Groop L, Altshuler D, Collins R, Lathrop GM, Melander O, Salomaa V, Peltonen L, Orho-Melander M, Ordovas JM, Boehnke M, Abecasis GR, Mohlke KL, Cupples LA.
Kathiresan S, et al.
Nat Genet. 2009 Jan;41(1):56-65. doi: 10.1038/ng.291. Epub 2008 Dec 7.
Nat Genet. 2009.
PMID: 19060906
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