The Cys(311)Ser polymorphism of paraoxonase 2 (PON2) is associated with albumin-to-creatinine ratio (ACR) in Mexican Americans

Nephrology Dialysis Transplantation

Volumn 23, Issue 1, 2008, Pages 416-417

  Thameem, Farook ^a   Puppala, Sobha ^c   Arar, Nedal H ^a   Farook, Vidya S ^c   Stern, Michael P ^b   Blangero, John ^c   Duggirala, Ravindranath ^c   Abboud, Hanna E ^a  

^a UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO   (United States)

^b University of Texas Health Science Center   (United States)

^c SOUTHWEST FOUNDATION FOR BIOMEDICAL RESEARCH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARYLDIALKYLPHOSPHATASE 2; CYSTEINE; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; SERINE; TRIACYLGLYCEROL; ARYLDIALKYLPHOSPHATASE; CREATININE; PON2 PROTEIN, HUMAN;

BLOOD PRESSURE MEASUREMENT; BODY MASS; CARDIOVASCULAR DISEASE; CORRELATION ANALYSIS; DISEASE ASSOCIATION; DNA POLYMORPHISM; ENZYME ACTIVITY; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC CODE; GENETIC VARIABILITY; GENOTYPE; HIGH RISK POPULATION; HISPANIC; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; INTRON; LETTER; MICROALBUMINURIA; MICROANGIOPATHY; NON INSULIN DEPENDENT DIABETES MELLITUS; OXIDATIVE STRESS; PATHOGENESIS; PATHOPHYSIOLOGY; PHENOTYPE; PRIORITY JOURNAL; QUANTITATIVE TRAIT; SYSTOLIC BLOOD PRESSURE; ALBUMINURIA; FEMALE; GENETIC POLYMORPHISM; GENETICS; MALE; MIDDLE AGED; URINE;

ALBUMINURIA; ARYLDIALKYLPHOSPHATASE; CREATININE; DIABETES MELLITUS, TYPE 2; FEMALE; HUMANS; MALE; MEXICAN AMERICANS; MIDDLE AGED; POLYMORPHISM, GENETIC;

EID: 44449170079     PISSN: 09310509     EISSN: 14602385     Source Type: Journal    
DOI: 10.1093/ndt/gfm633     Document Type: Letter

References (5)

1. Li H, Liu De, Liang C. Paraoxonase gene polymorphisms, oxidative stress, and diseases. J Mol Med 2003; 81: 766-779
2. Calle R, McCarthy MI, Banerjee P et al. Paraoxonase 2 (PON2) polymorphisms and development of renal dysfunction in type 2 diabetes: UKPDS 76. Diabetologia 2006; 49: 2892-2899
3. Puppala S, Dodd GD, Fowler S et al. A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans. Am J Hum Genet 2006; 78: 377-392
4. Lehman DM, Leach RJ, Johnson-Pais T et al. Evaluation of tight junction protein 1 encoding zona occludens 1 as a candidate gene for albuminuria in a Mexican American population. Exp Clin Endocrinol Diabetes 2006; 114: 432-437
5. Almasy L, Blangero J. Exploring positional candidate genes: linkage conditional on measured genotype. Behav Genet 2004; 34: 173-177