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Results: 1 to 20 of 44

1.

Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.

Sabater-Lleal M, Huang J, Chasman D, Naitza S, Dehghan A, Johnson AD, Teumer A, Reiner AP, Folkersen L, Basu S, Rudnicka AR, Trompet S, Mälarstig A, Baumert J, Bis JC, Guo X, Hottenga JJ, Shin SY, Lopez LM, Lahti J, Tanaka T, Yanek LR, Oudot-Mellakh T, Wilson JF, Navarro P, Huffman JE, Zemunik T, Redline S, Mehra R, Pulanic D, Rudan I, Wright AF, Kolcic I, Polasek O, Wild SH, Campbell H, Curb JD, Wallace R, Liu S, Eaton CB, Becker DM, Becker LC, Bandinelli S, Räikkönen K, Widen E, Palotie A, Fornage M, Green D, Gross M, Davies G, Harris SE, Liewald DC, Starr JM, Williams FM, Grant PJ, Spector TD, Strawbridge RJ, Silveira A, Sennblad B, Rivadeneira F, Uitterlinden AG, Franco OH, Hofman A, van Dongen J, Willemsen G, Boomsma DI, Yao J, Swords Jenny N, Haritunians T, McKnight B, Lumley T, Taylor KD, Rotter JI, Psaty BM, Peters A, Gieger C, Illig T, Grotevendt A, Homuth G, Völzke H, Kocher T, Goel A, Franzosi MG, Seedorf U, Clarke R, Steri M, Tarasov KV, Sanna S, Schlessinger D, Stott DJ, Sattar N, Buckley BM, Rumley A, Lowe GD, McArdle WL, Chen MH, Tofler GH, Song J, Boerwinkle E, Folsom AR, Rose LM, Franco-Cereceda A, Teichert M, Ikram MA, Mosley TH, Bevan S, Dichgans M, Rothwell PM, Sudlow CL, Hopewell JC, Chambers JC, Saleheen D, Kooner JS, Danesh J, Nelson CP, Erdmann J, Reilly MP, Kathiresan S, Schunkert H, Morange PE, Ferrucci L, Eriksson JG, Jacobs D, Deary IJ, Soranzo N, Witteman JC, de Geus EJ, Tracy RP, Hayward C, Koenig W, Cucca F, Jukema JW, Eriksson P, Seshadri S, Markus HS, Watkins H, Samani NJ; VTE Consortium; STROKE Consortium; Wellcome Trust Case Control Consortium 2 (WTCCC2); C4D Consortium; CARDIoGRAM Consortium, Wallaschofski H, Smith NL, Tregouet D, Ridker PM, Tang W, Strachan DP, Hamsten A, O'Donnell CJ.

Circulation. 2013 Sep 17;128(12):1310-24. doi: 10.1161/CIRCULATIONAHA.113.002251. Epub 2013 Aug 22.

PMID:
23969696
[PubMed - indexed for MEDLINE]
2.

HIV-1 Vpr enhances PPARβ/δ-mediated transcription, increases PDK4 expression, and reduces PDC activity.

Shrivastav S, Zhang L, Okamoto K, Lee H, Lagranha C, Abe Y, Balasubramanyam A, Lopaschuk GD, Kino T, Kopp JB.

Mol Endocrinol. 2013 Sep;27(9):1564-76. doi: 10.1210/me.2012-1370. Epub 2013 Jul 10.

PMID:
23842279
[PubMed - indexed for MEDLINE]
3.

Single nucleotide polymorphism in CPT1B and CPT2 genes and its association with blood carnitine levels in acute myocardial infarction patients.

Khan HA, Alhomida AS.

Gene. 2013 Jul 1;523(1):76-81. doi: 10.1016/j.gene.2013.03.086. Epub 2013 Apr 6.

PMID:
23566841
[PubMed - indexed for MEDLINE]
4.

A common haplotype of carnitine palmitoyltransferase 1b is associated with the metabolic syndrome.

Auinger A, Rubin D, Sabandal M, Helwig U, Rüther A, Schreiber S, Foelsch UR, Döring F, Schrezenmeir J.

Br J Nutr. 2013 Mar 14;109(5):810-5. doi: 10.1017/S0007114512002656. Epub 2012 Jul 19.

PMID:
22809552
[PubMed - indexed for MEDLINE]
5.

Exertional rhabdomyolysis: a clinical review with a focus on genetic influences.

Landau ME, Kenney K, Deuster P, Campbell W.

J Clin Neuromuscul Dis. 2012 Mar;13(3):122-36. doi: 10.1097/CND.0b013e31822721ca. Review.

PMID:
22538307
[PubMed - indexed for MEDLINE]
6.

TCRA, P2RY11, and CPT1B/CHKB associations in Chinese narcolepsy.

Han F, Lin L, Li J, Aran A, Dong SX, An P, Zhao L, Li QY, Yan H, Wang JS, Gao HY, Li M, Gao ZC, Strohl KP, Mignot E.

Sleep Med. 2012 Mar;13(3):269-72. doi: 10.1016/j.sleep.2011.06.020. Epub 2011 Dec 15.

PMID:
22177342
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Single nucleotide polymorphisms of matrix metalloproteinase 9 (MMP9) and tumor protein 73 (TP73) interact with Epstein-Barr virus in chronic lymphocytic leukemia: results from the European case-control study EpiLymph.

Casabonne D, Reina O, Benavente Y, Becker N, Maynadié M, Foretová L, Cocco P, González-Neira A, Nieters A, Boffetta P, Middeldorp JM, de Sanjose S.

Haematologica. 2011 Feb;96(2):323-7. doi: 10.3324/haematol.2010.031161. Epub 2010 Nov 3.

PMID:
21048031
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression.

Hendrickson SL, Lautenberger JA, Chinn LW, Malasky M, Sezgin E, Kingsley LA, Goedert JJ, Kirk GD, Gomperts ED, Buchbinder SP, Troyer JL, O'Brien SJ.

PLoS One. 2010 Sep 21;5(9):e12862. doi: 10.1371/journal.pone.0012862.

PMID:
20877624
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.

Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B, Yusuf S, Gerstein HC, Engert JC, Anand S; DREAM investigators.

Diabetes Care. 2010 Oct;33(10):2250-3. doi: 10.2337/dc10-0452. Epub 2010 Jul 13.

PMID:
20628086
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Replacement of C305 in heart/muscle-type isozyme of human carnitine palmitoyltransferase I with aspartic acid and other amino acids.

Matsuo T, Yamamoto A, Yamamoto T, Otsuki K, Yamazaki N, Kataoka M, Terada H, Shinohara Y.

Biochem Genet. 2010 Apr;48(3-4):193-201. doi: 10.1007/s10528-009-9301-z. Epub 2009 Nov 25.

PMID:
19937377
[PubMed - indexed for MEDLINE]
11.

Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.

Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M, Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ, Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S, Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD, Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE, Hingorani AD; ASCOT investigators; NORDIL investigators; BRIGHT Consortium.

Am J Hum Genet. 2009 Nov;85(5):628-42. doi: 10.1016/j.ajhg.2009.10.014.

PMID:
19913121
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Association of the CPT1B gene with skeletal muscle fat infiltration in Afro-Caribbean men.

Miljkovic I, Yerges LM, Li H, Gordon CL, Goodpaster BH, Kuller LH, Nestlerode CS, Bunker CH, Patrick AL, Wheeler VW, Zmuda JM.

Obesity (Silver Spring). 2009 Jul;17(7):1396-401. doi: 10.1038/oby.2008.677. Epub 2009 Feb 19.

PMID:
19553926
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Polymorphism located between CPT1B and CHKB, and HLA-DRB1*1501-DQB1*0602 haplotype confer susceptibility to CNS hypersomnias (essential hypersomnia).

Miyagawa T, Honda M, Kawashima M, Shimada M, Tanaka S, Honda Y, Tokunaga K.

PLoS One. 2009;4(4):e5394. doi: 10.1371/journal.pone.0005394. Epub 2009 Apr 30.

PMID:
19404393
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic leukemia.

Enjuanes A, Benavente Y, Bosch F, Martín-Guerrero I, Colomer D, Pérez-Alvarez S, Reina O, Ardanaz MT, Jares P, García-Orad A, Pujana MA, Montserrat E, de Sanjosé S, Campo E.

Cancer Res. 2008 Dec 15;68(24):10178-86. doi: 10.1158/0008-5472.CAN-08-2221.

PMID:
19074885
[PubMed - indexed for MEDLINE]
Free Article
15.

Physiogenomic comparison of edema and BMI in patients receiving rosiglitazone or pioglitazone.

Ruaño G, Bernene J, Windemuth A, Bower B, Wencker D, Seip RL, Kocherla M, Holford TR, Petit WA, Hanks S.

Clin Chim Acta. 2009 Feb;400(1-2):48-55. doi: 10.1016/j.cca.2008.10.009. Epub 2008 Oct 26.

PMID:
18996102
[PubMed - indexed for MEDLINE]
16.

A genome-wide association study for late-onset Alzheimer's disease using DNA pooling.

Abraham R, Moskvina V, Sims R, Hollingworth P, Morgan A, Georgieva L, Dowzell K, Cichon S, Hillmer AM, O'Donovan MC, Williams J, Owen MJ, Kirov G.

BMC Med Genomics. 2008 Sep 29;1:44. doi: 10.1186/1755-8794-1-44.

PMID:
18823527
[PubMed]
Free PMC Article
17.

Variant between CPT1B and CHKB associated with susceptibility to narcolepsy.

Miyagawa T, Kawashima M, Nishida N, Ohashi J, Kimura R, Fujimoto A, Shimada M, Morishita S, Shigeta T, Lin L, Hong SC, Faraco J, Shin YK, Jeong JH, Okazaki Y, Tsuji S, Honda M, Honda Y, Mignot E, Tokunaga K.

Nat Genet. 2008 Nov;40(11):1324-8. doi: 10.1038/ng.231. Epub 2008 Sep 28.

PMID:
18820697
[PubMed - indexed for MEDLINE]
18.

Multiple genetic variants along candidate pathways influence plasma high-density lipoprotein cholesterol concentrations.

Lu Y, Dollé ME, Imholz S, van 't Slot R, Verschuren WM, Wijmenga C, Feskens EJ, Boer JM.

J Lipid Res. 2008 Dec;49(12):2582-9. doi: 10.1194/jlr.M800232-JLR200. Epub 2008 Jul 25.

PMID:
18660489
[PubMed - indexed for MEDLINE]
Free Article
19.

Homozygous carnitine palmitoyltransferase 1b (muscle isoform) deficiency is lethal in the mouse.

Ji S, You Y, Kerner J, Hoppel CL, Schoeb TR, Chick WS, Hamm DA, Sharer JD, Wood PA.

Mol Genet Metab. 2008 Mar;93(3):314-22. Epub 2007 Nov 19.

PMID:
18023382
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Substitutions of three amino acids in human heart/muscle type carnitine palmitoyltransferase I caused by single nucleotide polymorphisms.

Yamazaki N, Matsuo T, Kurata M, Suzuki M, Fujiwaki T, Yamaguchi S, Terada H, Shinohara Y.

Biochem Genet. 2008 Feb;46(1-2):54-63. Epub 2007 Nov 7.

PMID:
17987377
[PubMed - indexed for MEDLINE]

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