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Hydroxykynureninuria: Disease Bioinformatics
Research of Hydroxykynureninuria has been linked to Inborn Errors Of Metabolism, Pellagra, Metabolic Diseases, Kidney Calculi, Tyrosine Transaminase Deficiency Disease. The study of Hydroxykynureninuria has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Hydroxykynureninuria include Excretion, Glycolysis. These pathways complement our catalog of research reagents for the study of Hydroxykynureninuria including antibodies and ELISA kits against KYNU.
Hydroxykynureninuria Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Hydroxykynureninuria below!
For more information on how to use Laverne, please read the How to Guide
Top Research Reagents
We have 19 products for the study of Hydroxykynureninuria that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Applications IHC, IHC-P
Hydroxykynureninuria has been researched against:
Hydroxykynureninuria has been linked to:
Hydroxykynureninuria has been studied in relation to diseases such as:
Alternate NamesHydroxykynureninuria is also known as hydroxykynureninuria, kynureninase deficiency, xanthurenic aciduria.