homogentisic acid/necrosis

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NakalaMajaribio ya klinikiHati miliki

Chagua aina ya aina

2 matokeo

Alkaptonuria--a review of surgical and autopsy pathology.

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Ingia / Ingia

Alkaptonuria is a rare, inherited defect of homogentisic acid 1,2-dioxygenase that leads to the widespread deposition of polymeric homogentisic acid, and clinical symptoms from degeneration of joints and the aortic valve. Pathological descriptions are few and mainly those of late-stage changes

Chronic liver disease in murine hereditary tyrosinemia type 1 induces resistance to cell death.

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Ingia / Ingia

The murine model of hereditary tyrosinemia type 1 (HT1) was used to analyze the relationship between chronic liver disease and programmed cell death in vivo. In healthy fumarylacetoacetate hydrolase deficient mice (Fah(-/-)), protected from liver injury by the drug 2-(2-

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Herbal & Natural Medicine

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