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Hydroxyproline metabolism in mouse models of primary hyperoxaluria

Primary hyperoxaluria type 1 (PH1) and type 2 (PH2) are rare genetic diseases that result from deficiencies in glyoxylate metabolism. The increased oxalate synthesis that occurs can lead to kidney stone formation, deposition of calcium oxalate in the kidney and other tissues, and renal failure. Hydr...

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Détails bibliographiques
Auteurs principaux: Knight, John, Holmes, Ross P., Cramer, Scott D., Takayama, Tatsuya, Salido, Eduardo
Format: Artigo
Langue:Inglês
Publié: American Physiological Society 2012
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3311317/
https://ncbi.nlm.nih.gov/pubmed/22189945
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajprenal.00473.2011
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