https://pmc.ncbi.nlm.nih.gov/articles/PMC21376/
Hepatocyte injury in tyrosinemia type 1 is induced by fumarylacetoacetate and is inhibited by...
Tyrosinemia type 1, caused by mutations in the fumarylacetoacetate hydrolase gene (Fah), is characterized by severe liver injury. We earlier developed a...
https://pubmed.ncbi.nlm.nih.gov/23138988/
Fumarylacetoacetate inhibits the initial step of the base excision repair pathway: implication for...
Hereditary tyrosinemia type I (HT1) is an autosomal recessive disease caused by a deficiency in human fumarylacetoacetate (FAA) hydrolase (FAH), which is the...
base excision repair
https://pubchem.ncbi.nlm.nih.gov/protein/Q1YGK7
Fumarylacetoacetate hydrolase family protein (Aurantimonas manganoxydans SI85-9A1) | Protein Target...
Protein target information for Fumarylacetoacetate hydrolase family protein (Aurantimonas manganoxydans SI85-9A1). Find diseases associated with this...
hydrolasefamilyproteintarget