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Common variants in glyoxalase I do not increase chronic pancreatitis risk.

Tom Kaune | Marcus Hollenbach | Bettina Keil | Jian-Min Chen | Emmanuelle Masson | Carla Becker | Marko Damm | Claudia Ruffert | Robert Grützmann | Albrecht Hoffmeister | Rene H M Te Morsche | Giulia Martina Cavestro | Raffaella Alessia Zuppardo | Adrian Saftoiu | Ewa Malecka-Panas | Stanislaw Głuszek | Peter Bugert | Markus M Lerch | Frank Ulrich Weiss | Wen-Bin Zou | Zhuan Liao | Peter Hegyi | Joost Ph Drenth | Jan Riedel | Claude Férec | Markus Scholz | Holger Kirsten | Andrea Tóth | Maren Ewers | Heiko Witt | Heidi Griesmann | Patrick Michl | Jonas Rosendahl
PloS one | 2019

Chronic pancreatitis (CP) may be caused by oxidative stress. An important source of reactive oxygen species (ROS) is the methylglyoxal-derived formation of advanced glycation endproducts (AGE). Methylglyoxal is detoxified by Glyoxalase I (GLO1). A reduction in GLO1 activity results in increased ROS. Single nucleotide polymorphisms (SNPs) of GLO1 have been linked to various inflammatory diseases. Here, we analyzed whether common GLO1 variants are associated with alcoholic (ACP) and non-alcoholic CP (NACP).

Pubmed ID: 31661534

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GraphPad Prism (tool)

RRID:SCR_002798

Statistical analysis software that combines scientific graphing, comprehensive curve fitting (nonlinear regression), understandable statistics, and data organization. Designed for biological research applications in pharmacology, physiology, and other biological fields for data analysis, hypothesis testing, and modeling.

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