Associated Papers
Regulation of Human Hydrolases and Its Implications in Pharmacokinetics and Pharmacodynamics.
Jung SM et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals, 2024
A Case-Control Study Supports Genetic Contribution of the PON Gene Family in Obesity and Metabolic Dysfunction Associated Steatotic Liver Disease.
Van Dijck E et al.
Antioxidants (basel, Switzerland), 2024
39334710 (PubMed )
Supplement: antioxidants-13-01051-s001.zip › antioxidants-3169066-supplementary.pdf
Paraoxonase 3: Structure and Its Role in Pathophysiology of Coronary Artery Disease.
Priyanka K et al.
Biomolecules, 2019
Exome Sequencing in BRCA1- and BRCA2-Negative Greek Families Identifies MDM1 and NBEAL1 as Candidate Risk Genes for Hereditary Breast Cancer.
Glentis S et al.
Frontiers in Genetics, 2019
31681433 (PubMed )
Supplement: DataSheet_1.xlsx › Supplemetary_Table_10
Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations.
Bujakowska KM et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2017
27735924 (PubMed )
Supplement: NIHMS819557-supplement-Supplementary___Appendix__online_only_material__etc__.pdf
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A8-A07G-01A.domain
Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencing.
Kenna KP et al.
Journal of Medical Genetics, 2013
23881933 (PubMed )
Supplement: jmedgenet-2013-101795-s1.pdf
Paraoxonase (PON1 and PON3) Polymorphisms: Impact on Liver Expression and Atorvastatin-Lactone Hydrolysis.
Riedmaier S et al.
Frontiers in Pharmacology, 2011
Paraoxonase gene mutations in amyotrophic lateral sclerosis.
Ticozzi N et al.
Annals of Neurology, 2010
Paraoxonase 1, 2 and 3 DNA variants and susceptibility to childhood inflammatory bowel disease.
Sanchez R et al.
Gut, 2006
Identification of paraoxonase 3 gene (PON3) missense mutations in a population of southern Italy.
Campo S et al.
Mutation Research, 2004
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