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Items: 1 to 20 of 85

1.

MYLIP p.N342S polymorphism is not associated with lipid profile in the Brazilian population.

Santos PC, Oliveira TG, Lemos PA, Mill JG, Krieger JE, Pereira AC.

Lipids Health Dis. 2012 Jun 28;11:83. doi: 10.1186/1476-511X-11-83.

2.

The MYLIP p.N342S polymorphism is associated with response to lipid-lowering therapy in Brazilian patients with familial hypercholesterolemia.

Santos PC, Morgan AC, Jannes CE, Krieger JE, Santos RD, Pereira AC.

Pharmacogenet Genomics. 2014 Nov;24(11):548-55. doi: 10.1097/FPC.0000000000000089.

3.

The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humans.

Weissglas-Volkov D, Calkin AC, Tusie-Luna T, Sinsheimer JS, Zelcer N, Riba L, Tino AM, Ordoñez-Sánchez ML, Cruz-Bautista I, Aguilar-Salinas CA, Tontonoz P, Pajukanta P.

J Clin Invest. 2011 Aug;121(8):3062-71. doi: 10.1172/JCI45504. Epub 2011 Jul 18.

4.

IDOL N342S Variant, Atherosclerosis Progression and Cardiovascular Disorders in the Italian General Population.

Dhyani A, Tibolla G, Baragetti A, Garlaschelli K, Pellegatta F, Grigore L, Norata GD, Catapano AL.

PLoS One. 2015 Apr 30;10(4):e0122414. doi: 10.1371/journal.pone.0122414. eCollection 2015.

5.

Several genetic polymorphisms interact with overweight/obesity to influence serum lipid levels.

Yin RX, Wu DF, Miao L, Aung LH, Cao XL, Yan TT, Long XJ, Liu WY, Zhang L, Li M.

Cardiovasc Diabetol. 2012 Oct 8;11:123. doi: 10.1186/1475-2840-11-123.

6.

Association between the C242T polymorphism in the p22phox gene with arterial stiffness in the Brazilian population.

de Oliveira Alvim R, Santos PC, Dias RG, Rodrigues MV, de Sa Cunha R, Mill JG, Junior WN, Krieger JE, Pereira AC.

Physiol Genomics. 2012 May 1;44(10):587-92. doi: 10.1152/physiolgenomics.00122.2011. Epub 2012 Apr 10.

7.

Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3.

Proust C, Empana JP, Boutouyrie P, Alivon M, Challande P, Danchin N, Escriou G, Esslinger U, Laurent S, Li Z, Pannier B, Regnault V, Thomas F, Jouven X, Cambien F, Lacolley P.

Circ Cardiovasc Genet. 2015 Aug;8(4):628-36. doi: 10.1161/CIRCGENETICS.114.000979. Epub 2015 Jul 9.

8.

The effect of a single nucleotide polymorphism of the CYP4F2 gene on blood pressure and 20-hydroxyeicosatetraenoic acid excretion after weight loss.

Ward NC, Croft KD, Puddey IB, Phillips M, van Bockxmeer F, Beilin LJ, Barden AE.

J Hypertens. 2014 Jul;32(7):1495-502; discussion 1502. doi: 10.1097/HJH.0000000000000208.

PMID:
24984178
9.

Genetic variant of V825I in the ATP-binding cassette transporter A1 gene and serum lipid levels in the Guangxi Bai Ku Yao and Han populations.

Cao XL, Yin RX, Wu DF, Miao L, Aung LH, Hu XJ, Li Q, Yan TT, Lin WX, Pan SL.

Lipids Health Dis. 2011 Jan 19;10:14. doi: 10.1186/1476-511X-10-14.

10.

The role of common variants of the cholesteryl ester transfer protein gene in left main coronary artery disease.

Kolovou G, Vasiliadis I, Kolovou V, Karakosta A, Mavrogeni S, Papadopoulou E, Papamentzelopoulos S, Giannakopoulou V, Marvaki A, Degiannis D, Bilianou H.

Lipids Health Dis. 2011 Sep 7;10:156. doi: 10.1186/1476-511X-10-156.

11.

+294T/C polymorphism in the PPAR-delta gene is associated with risk of coronary artery disease in normolipidemic Tunisians.

Jguirim-Souissi I, Jelassi A, Hrira Y, Najah M, Slimani A, Addad F, Hassine M, Hamda KB, Maatouk F, Rouis M, Slimane MN.

Genet Mol Res. 2010 Jul 13;9(3):1326-33. doi: 10.4238/vol9-3gmr831.

12.

Association of single nucleotide polymorphism rs6903956 on chromosome 6p24.1 with coronary artery disease and lipid levels in different ethnic groups of the Singaporean population.

Tayebi N, Ke T, Foo JN, Friedlander Y, Liu J, Heng CK.

Clin Biochem. 2013 Jun;46(9):755-9. doi: 10.1016/j.clinbiochem.2013.01.004. Epub 2013 Jan 18.

PMID:
23337689
13.

Lipid profile and apolipoprotein E polymorphism in essential hypertension.

Bhavani AB, Sastry KB, Reddy NK, Padma T.

Indian Heart J. 2005 Mar-Apr;57(2):151-7.

PMID:
16013355
14.
15.

[Genetic factors in myocardial infarction--Results from a candidate gene and a genome-wide approach between beta blockers].

Hengstenberg C, Bröckel U, Holmer S, Mayer B, Fischer M, Baessler A, Erdmann J, Lieb W, Löwel H, Riegger G, Schunkert H.

Herz. 2002 Nov;27(7):649-61. German. Erratum in: Herz. 2003 May;28(3):266.

PMID:
12439636
16.

Common variants in the ATP2B1 gene are associated with hypertension and arterial stiffness in Chinese population.

Wang Y, Zhang Y, Li Y, Zhou X, Wang X, Gao P, Jin L, Zhang X, Zhu D.

Mol Biol Rep. 2013 Feb;40(2):1867-73. doi: 10.1007/s11033-012-2242-3. Epub 2012 Oct 19.

PMID:
23079715
17.

[Association and linkage analysis between the S447X polymorphism of LPL gene and serum lipids, blood pressures in twins].

Huang AQ, Hu YH, Xu B, Zhan SY, Lv J, Qin Y, Cao WH, Li LM.

Beijing Da Xue Xue Bao. 2005 Dec 18;37(6):585-90. Chinese.

18.

[Geographical characteristics of single nucleotide polymorphism of candidate genes associated with coronary artery disease in Chinese Han population].

Wang SH, Cui HB, Wang DQ, Chen XM, Zhang HK, Cui CC, Chen XY, Liu XH, Zhang Z, Bai F, Jb M.

Zhonghua Xin Xue Guan Bing Za Zhi. 2008 Jan;36(1):24-9. Chinese.

PMID:
19099922
19.

APOE polymorphism is associated with lipid profile, but not with arterial stiffness in the general population.

Alvim RO, Freitas SR, Ferreira NE, Santos PC, Cunha RS, Mill JG, Krieger JE, Pereira AC.

Lipids Health Dis. 2010 Nov 8;9:128. doi: 10.1186/1476-511X-9-128.

20.

Scavenger receptor class B type 1 gene rs5888 single nucleotide polymorphism and the risk of coronary artery disease and ischemic stroke: a case-control study.

Wu DF, Yin RX, Cao XL, Chen WX, Aung LH, Wang W, Huang KK, Huang P, Zeng XN, Wu J.

Int J Med Sci. 2013 Oct 16;10(12):1771-7. doi: 10.7150/ijms.7044. eCollection 2013.

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