Varaico: Literature-Extracted Genetic Variants

Gene:PON2
Variant:p.A50T
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PON2

NM_000305.3:p.A50T

Associated Papers

Paraoxonase Role in Human Neurodegenerative Diseases.

Reichert CO et al.

Antioxidants (basel, Switzerland), 2020

WTAP and BIRC3 are involved in the posttranscriptional mechanisms that impact on the expression and activity of the human lactonase PON2.

Carusone TM et al.

Cell Death & Disease, 2020

32382056 (PubMed )
Supplement: 41419_2020_2504_MOESM1_ESM.docx

Paraoxonase-2 variants potentially influence insulin resistance, beta-cell function, and their interrelationships with alanine aminotransferase in type 2 diabetes.

Qujeq D et al.

Journal of Research in Medical Sciences : the Official Journal of Isfahan University of Medical Sciences, 2018

PON gene polymorphisms and ischaemic stroke: a systematic review and meta analysis.

Liu H et al.

International Journal of Stroke : Official Journal of the International Stroke Society, 2013

Paraoxonase gene polymorphism in south-western Korean population.

Shin BS

Journal of Korean Medical Science, 2009

The paraoxonase gene polymorphism in stroke patients and lipid profile.

Shin BS et al.

Acta Neurologica Scandinavica, 2008

Study of the relationship between gene polymorphisms of paraoxonase 2 and stroke in a Chinese population.

Xu HW et al.

Cerebrovascular Diseases (basel, Switzerland), 2008

Paraoxonase (PON)1 192R allele carriage is associated with reduced risk of inflammatory bowel disease.

Karban A et al.

Digestive Diseases and Sciences, 2007

[Relationship between single nucleotide polymorphisms of paraoxonase 2 and stroke].

Xu HW et al.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2007

Paraoxonase 1, 2 and 3 DNA variants and susceptibility to childhood inflammatory bowel disease.

Sanchez R et al.

Gut, 2006

[The significance of IL-13 gene +2044G/A mutation in patients with inflammatory bowel disease].

Waterman M et al.

Harefuah, 2006

Case-control study of genotypes in multiple chemical sensitivity: CYP2D6, NAT1, NAT2, PON1, PON2 and MTHFR.

McKeown-Eyssen G et al.

International Journal of Epidemiology, 2004

Association of PON2 and PON3 polymorphism with risk of developing cataract.

Baig A et al.

Saudi Journal of Ophthalmology : Official Journal of the Saudi Ophthalmological Society, 0

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."