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Items: 1 to 20 of 577

1.

Polymorphism in ERCC1 confers susceptibility of coronary artery disease and severity of coronary artery atherosclerosis in a Chinese Han population.

Zhang S, Wang XB, Han YD, Xiong CL, Zhou Y, Wang C, Liu ZJ, Yang N, Zheng F.

Sci Rep. 2017 Jul 25;7(1):6407. doi: 10.1038/s41598-017-06732-9.

2.

A Nutrigenomic Approach to Non-Alcoholic Fatty Liver Disease.

Dongiovanni P, Valenti L.

Int J Mol Sci. 2017 Jul 16;18(7). pii: E1534. doi: 10.3390/ijms18071534. Review.

3.

Tribbles homolog 1 enhances cholesterol efflux from oxidized low-density lipoprotein-loaded THP-1 macrophages.

Fu Y, Zhao Y, Huang B.

Exp Ther Med. 2017 Jul;14(1):862-866. doi: 10.3892/etm.2017.4551. Epub 2017 Jun 7.

4.

The Association between Pediatric NAFLD and Common Genetic Variants.

Umano GR, Martino M, Santoro N.

Children (Basel). 2017 Jun 18;4(6). pii: E49. doi: 10.3390/children4060049. Review.

5.

Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth.

Hong X, Hao K, Ji H, Peng S, Sherwood B, Di Narzo A, Tsai HJ, Liu X, Burd I, Wang G, Ji Y, Caruso D, Mao G, Bartell TR, Zhang Z, Pearson C, Heffner L, Cerda S, Beaty TH, Fallin MD, Lee-Parritz A, Zuckerman B, Weeks DE, Wang X.

Nat Commun. 2017 Jun 9;8:15608. doi: 10.1038/ncomms15608.

6.

Genetic determinants of inherited susceptibility to hypercholesterolemia - a comprehensive literature review.

Paththinige CS, Sirisena ND, Dissanayake V.

Lipids Health Dis. 2017 Jun 2;16(1):103. doi: 10.1186/s12944-017-0488-4. Review.

7.

Epigenetic Patterns in Blood Associated With Lipid Traits Predict Incident Coronary Heart Disease Events and Are Enriched for Results From Genome-Wide Association Studies.

Hedman ÅK, Mendelson MM, Marioni RE, Gustafsson S, Joehanes R, Irvin MR, Zhi D, Sandling JK, Yao C, Liu C, Liang L, Huan T, McRae AF, Demissie S, Shah S, Starr JM, Cupples LA, Deloukas P, Spector TD, Sundström J, Krauss RM, Arnett DK, Deary IJ, Lind L, Levy D, Ingelsson E.

Circ Cardiovasc Genet. 2017 Jan;10(1). pii: e001487. doi: 10.1161/CIRCGENETICS.116.001487.

8.

The Relationship Between Coronary Artery Disease and Genetic Polymorphisms of Melanoma Inhibitory Activity 3.

Zaimkohan H, Keramatipour M, Mirhafez SR, Tavakkoly-Bazzaz J, Tahooni A, Piryaei M, Ghayour-Mobarhan M, Ghaderian SM.

Iran Red Crescent Med J. 2016 Feb 13;18(9):e31146. doi: 10.5812/ircmj.31146. eCollection 2016 Sep.

9.

Association between genetic loci linked to HDL-C levels and Indian patients with CAD: a pilot study.

Stanley A, Ponde CK, Rajani RM, Ashavaid TF.

Heart Asia. 2017 Jan 4;9(1):9-13. doi: 10.1136/heartasia-2016-010822. eCollection 2017.

10.

The genetic overlap between mood disorders and cardiometabolic diseases: a systematic review of genome wide and candidate gene studies.

Amare AT, Schubert KO, Klingler-Hoffmann M, Cohen-Woods S, Baune BT.

Transl Psychiatry. 2017 Jan 24;7(1):e1007. doi: 10.1038/tp.2016.261. Review.

11.

Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms.

Guo MH, Nandakumar SK, Ulirsch JC, Zekavat SM, Buenrostro JD, Natarajan P, Salem RM, Chiarle R, Mitt M, Kals M, Pärn K, Fischer K, Milani L, Mägi R, Palta P, Gabriel SB, Metspalu A, Lander ES, Kathiresan S, Hirschhorn JN, Esko T, Sankaran VG.

Proc Natl Acad Sci U S A. 2017 Jan 17;114(3):E327-E336. doi: 10.1073/pnas.1619052114. Epub 2016 Dec 28.

12.

Dietary Macronutrient Composition Directs ChREBP Isoform Expression and Glucose Metabolism in Mice.

Jois T, Howard V, Youngs K, Cowley MA, Sleeman MW.

PLoS One. 2016 Dec 19;11(12):e0168797. doi: 10.1371/journal.pone.0168797. eCollection 2016.

13.

Signatures of natural selection on genetic variants affecting complex human traits.

Zhang G, Muglia LJ, Chakraborty R, Akey JM, Williams SM.

Appl Transl Genom. 2013 Nov 7;2:78-94. eCollection 2013 Dec 1.

14.

Role of NCAN rs2228603 polymorphism in the incidence of nonalcoholic fatty liver disease: a case-control study.

Wu MJ, Yuan C, Lu LL, An BQ, Xuan SY, Xin YN.

Lipids Health Dis. 2016 Nov 26;15(1):207.

15.
16.

Exendin-4 Ameliorates Lipotoxicity-induced Glomerular Endothelial Cell Injury by Improving ABC Transporter A1-mediated Cholesterol Efflux in Diabetic apoE Knockout Mice.

Yin QH, Zhang R, Li L, Wang YT, Liu JP, Zhang J, Bai L, Cheng JQ, Fu P, Liu F.

J Biol Chem. 2016 Dec 16;291(51):26487-26501. Epub 2016 Oct 26.

PMID:
27784780
17.

Pharmacogenomics of statins: understanding susceptibility to adverse effects.

Kitzmiller JP, Mikulik EB, Dauki AM, Murkherjee C, Luzum JA.

Pharmgenomics Pers Med. 2016 Oct 3;9:97-106. eCollection 2016. Review.

18.

Association of KCTD10, MVK, and MMAB polymorphisms with dyslipidemia and coronary heart disease in Han Chinese population.

Sun J, Qian Y, Jiang Y, Chen J, Dai J, Jin G, Wang J, Hu Z, Liu S, Shen C, Shen H.

Lipids Health Dis. 2016 Oct 4;15(1):171.

19.

Uncoupling associations of risk alleles with endophenotypes and phenotypes: insights from the ApoB locus and heart-related traits.

Kulminski AM, Kernogitski Y, Culminskaya I, Loika Y, Arbeev KG, Bagley O, Duan M, Arbeeva L, Ukraintseva SV, Wu D, Stallard E, Yashin AI.

Aging Cell. 2017 Feb;16(1):61-72. doi: 10.1111/acel.12526. Epub 2016 Sep 28.

20.

The Genetic Landscape of Renal Complications in Type 1 Diabetes.

Sandholm N, Van Zuydam N, Ahlqvist E, Juliusdottir T, Deshmukh HA, Rayner NW, Di Camillo B, Forsblom C, Fadista J, Ziemek D, Salem RM, Hiraki LT, Pezzolesi M, Trégouët D, Dahlström E, Valo E, Oskolkov N, Ladenvall C, Marcovecchio ML, Cooper J, Sambo F, Malovini A, Manfrini M, McKnight AJ, Lajer M, Harjutsalo V, Gordin D, Parkkonen M; FinnDiane Study Group, Jaakko Tuomilehto, Lyssenko V, McKeigue PM, Rich SS, Brosnan MJ, Fauman E, Bellazzi R, Rossing P, Hadjadj S, Krolewski A, Paterson AD; DCCT/EDIC Study Group, Jose C. Florez, Hirschhorn JN, Maxwell AP; GENIE Consortium, David Dunger, Cobelli C, Colhoun HM, Groop L, McCarthy MI, Groop PH; SUMMIT Consortium.

J Am Soc Nephrol. 2017 Feb;28(2):557-574. doi: 10.1681/ASN.2016020231. Epub 2016 Sep 19.

PMID:
27647854

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