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4-hydroxyphenylpyruvic acid

Known as: (p-hydroxyphenyl)pyruvic acid, 4-hydroxy alpha-oxobenzenepropanoic acid, para-hydroxyphenylpyruvic acid 
National Institutes of Health

Papers overview

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2009
2009
Deficiencies of the pyruvate dehydrogenase complex enzyme and of the mitochondrial respiratory chain enzymes in humans both… 
2007
2007
Hereditary tyrosinemia I (HT I) is a genetic disorder of tyrosine metabolism characterized by progressive liver damage from… 
2003
2003
The activity of the enzyme 4-hydroxyphenylpyruvic acid dioxygenase (HPD) is regulated by transcription factors. Mutations in the… 
2003
2003
The activity of the enzyme 4-hydroxyphenylpyruvic acid dioxygenase (HPD) is regulated by transcription factors. Mutations in the… 
1996
1996
Sir: Transient neonatal tyrosinaemia is thought to be caused by late maturation of the hepatic enzymes 4-hydroxyphenylpyruvate… 
1980
1980
A low-phenylalanine diet was given for a period of three weeks to four untreated adult phenylketonurics with mental deficiency… 
Highly Cited
1976
Highly Cited
1976
A metabolic pathway for L-tyrosine catabolism involves 3,4-dihydroxyphenylacetic acid (homoprotocatechuic acid) as substrate for… 
1975
1975
The occurrence from a marine sponge of 4-hydroxyphenylpyruvic acid oxime is good evidence that an oxime (4) is the biogenetic…