19 results for author:"Senti M." in Literature citations
Results Customize
› Repeat search in UniProtKB (1)
| Post-genomic update on a classical candidate gene for coronary artery disease: ESR1. CARDIoGRAM Consortium Circ Cardiovasc Genet 4:647-654(2011) · Mapped (58) |
| A gain-of-function SNP in TRPC4 cation channel protects against myocardial infarction. Jung C., Gene G.G., Tomas M., Plata C., Selent J., Pastor M., Fandos C., Senti M., Lucas G., Elosua R. et al. Cardiovasc. Res. 91:465-471(2011) · Mapped (6) |
| Additive effect of multiple genetic variants on the risk of coronary artery disease. Lluis-Ganella C., Lucas G., Subirana I., Senti M., Jimenez-Conde J., Marrugat J., Tomas M., Elosua R. Rev Esp Cardiol 63:925-933(2010) · Mapped (78) |
| Qualitative assessment of previous evidence and an updated meta-analysis confirms lack of association between the ESR1 rs2234693 (PvuII) variant and coronary heart disease in men and women. Lluis-Ganella C., Lucas G., Subirana I., Escurriol V., Tomas M., Senti M., Sala J., Marrugat J., Elosua R. Atherosclerosis 207:480-486(2009) · Mapped (58) |
| Genetic variation in the KCNMA1 potassium channel alpha subunit as risk factor for severe essential hypertension and myocardial infarction. Tomas M., Vazquez E., Fernandez-Fernandez J.M., Subirana I., Plata C., Heras M., Vila J., Marrugat J., Valverde M.A., Senti M. J. Hypertens. 26:2147-2153(2008) · Mapped (15) |
| Association between paraoxonase-1 and paraoxonase-2 polymorphisms and the risk of acute myocardial infarction. Guxens M., Tomas M., Elosua R., Aldasoro E., Segura A., Fiol M., Sala J., Vila J., Fullana M., Senti M. et al. Rev Esp Cardiol 61:269-275(2008) · Mapped (11) |
| Relationship of classical and non-classical risk factors with genetic variants relevant to coronary heart disease. Manresa J.M., Zamora A., Tomas M., Senti M., Fito M., Covas M.I., Alcantara M., Latorre G., Escurriol V., Domingues S. et al. Eur J Cardiovasc Prev Rehabil 13:738-744(2006) · Mapped (34) |
| Protective effect of the KCNMB1 E65K genetic polymorphism against diastolic hypertension in aging women and its relevance to cardiovascular risk. Senti M., Fernandez-Fernandez J.M., Tomas M., Vazquez E., Elosua R., Marrugat J., Valverde M.A. Circ. Res. 97:1360-1365(2005) · Mapped (3) |
| Gain-of-function mutation in the KCNMB1 potassium channel subunit is associated with low prevalence of diastolic hypertension. Fernandez-Fernandez J.M., Tomas M., Vazquez E., Orio P., Latorre R., Senti M., Marrugat J., Valverde M.A. J. Clin. Invest. 113:1032-1039(2004) · UniProtKB (1) |
| Paraoxonase 1 gene 192 polymorphism, physical activity and lipoprotein in women. Manresa J.M., Tomas M., Ribes E., Pi-Figueras M., Aguilera A., Senti M., Marrugat J. Med Clin (Barc) 122:126-129(2004) · Mapped (3) |
| Antioxidant paraoxonase 1 activity in the metabolic syndrome. Senti M., Tomas M., Fito M., Weinbrenner T., Covas M.I., Sala J., Masia R., Marrugat J. J. Clin. Endocrinol. Metab. 88:5422-5426(2003) · Mapped (4) |
| The paraoxonase-1 codon 192 polymorphism is associated with fasting total cholesterol and LDL-cholesterol concentrations only in postmenopausal women. The REGICOR study. Senti M., Tomas M., Elosual R., Sala J., Masia R., Marrugat J. Clin. Chem. Lab. Med. 40:677-683(2002) · Mapped (3) |
| Paraoxonase1-192 polymorphism modulates the effects of regular and acute exercise on paraoxonase1 activity. Tomas M., Elosua R., Senti M., Molina L., Vila J., Anglada R., Fito M., Covas M.I., Marrugat J. J. Lipid Res. 43:713-720(2002) · Mapped (3) |
| Interaction between the Gln-Arg 192 variants of the paraoxonase gene and oleic acid intake as a determinant of high-density lipoprotein cholesterol and paraoxonase activity. Tomas M., Senti M., Elosua R., Vila J., Sala J., Masia R., Marrugat J. Eur. J. Pharmacol. 432:121-128(2001) · Mapped (3) |
| Physical activity modulates the combined effect of a common variant of the lipoprotein lipase gene and smoking on serum triglyceride levels and high-density lipoprotein cholesterol in men. Senti M., Elosua R., Tomas M., Sala J., Masia R., Ordovas J.M., Shen H., Marrugat J. Hum. Genet. 109:385-392(2001) · Mapped (9) |
| Relationship of age-related myocardial infarction risk and Gln/Arg 192 variants of the human paraoxonase1 gene: the REGICOR study. Senti M., Tomas M., Vila J., Marrugat J., Elosua R., Sala J., Masia R. Atherosclerosis 156:443-449(2001) · Mapped (3) |
| Paraoxonase1-192 polymorphism modulates the nonfatal myocardial infarction risk associated with decreased HDLs. Senti M., Tomas M., Marrugat J., Elosua R. Arterioscler. Thromb. Vasc. Biol. 21:415-420(2001) · Mapped (3) |
| Risk of myocardial infarction associated with Gln/Arg 192 polymorphism in the human paraoxonase gene and diabetes mellitus. The REGICOR Investigators. Aubo C., Senti M., Marrugat J., Tomas M., Vila J., Sala J., Masia R. Eur. Heart J. 21:33-38(2000) · Mapped (1) |
| Platelet glycoprotein IIb/IIIa genetic polymorphism is associated with plasma fibrinogen levels in myocardial infarction patients. The REGICOR Investigators. Senti M., Aubo C., Bosch M., Pavesi M., Pena A., Masia R., Marrugat J. Clin. Biochem. 31:647-651(1998) · Mapped (6) |