Paraoxonase Arg 192 allele is an independent risk factor for three-vessel stenosis of coronary artery disease

Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia

(2010) Muhammad Ajmal et al.   MOLECULAR BIOLOGY REPORTS

Association of homocysteine thiolactonase activity and PON1 polymorphisms with the severity of acute coronary syndrome

(2009) Nadia Koubaa et al.   CLINICAL BIOCHEMISTRY

The relationship between paraoxonase1-192 polymorphism and activity with coronary artery disease

(2009) Randa H. Mohamed et al.   CLINICAL BIOCHEMISTRY

Non-diabetic metabolic syndrome and obesity do not affect serum paraoxonase and arylesterase activities but do affect oxidative stress and inflammation

(2009) Suzan Tabur et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

Association of genetic variants in Methylenetetrahydrofolate Reductase and Paraoxonase-1 genes with homocysteine, folate and vitamin B12 in coronary artery disease

(2009) Makbule Aydin et al.   MOLECULAR AND CELLULAR BIOCHEMISTRY

Genetic variants on apolipoprotein gene cluster influence triglycerides with a risk of coronary artery disease among Indians

(2009) Manickaraj AshokKumar et al.   MOLECULAR BIOLOGY REPORTS

Butyrylcholinesterase K variant and the APOE-ε4 allele work in synergy to increase the risk of coronary artery disease especially in diabetic patients

(2009) Asad Vaisi-Raygani et al.   MOLECULAR BIOLOGY REPORTS

Serum butyrylcholinesterase activity and phenotype associations with lipid profile in stroke patients

(2008) Asad Vaisi-Raygani et al.   CLINICAL BIOCHEMISTRY

Butyrylcholinesterase K variants increase the risk of coronary artery disease in the population of western Iran

(2008) A. Vaisi‐Raygani et al.   SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION