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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
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Related topics
Related topics
2 relations
Narrower (1)
4-hydroxyphenylpyruvate
Broader (1)
Phenylpyruvic Acids
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Determination of α-keto acids in pork meat and Iberian ham via tandem mass spectrometry.
F. Hidalgo
,
J. Navarro
,
R. Delgado
,
R. Zamora
Food Chemistry
2013
Corpus ID: 20487027
2007
2007
Manifestation of hawkinsinuria in a patient compound heterozygous for hawkinsinuria and tyrosinemia III.
C. Item
,
I. Mihalek
,
+4 authors
O. Bodamer
Molecular Genetics and Metabolism
2007
Corpus ID: 23982690
1998
1998
Increased excretion of aromatic amino acid catabolites in animals infected with Trypanosoma brucei evansi.
A. el Sawalhy
,
J. Seed
,
J. Hall
,
H. El Attar
Journal of Parasitology
1998
Corpus ID: 39988932
Aromatic amino acid catabolism by Trypanosoma brucei evansi was investigated in vivo using C3HeB/FeJ mice. The major catabolites…
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1997
1997
In vivo correction with recombinant adenovirus of 4-hydroxyphenylpyruvic acid dioxygenase deficiencies in strain III mice.
S. Kubo
,
K. Kiwaki
,
+7 authors
F. Endo
Human Gene Therapy
1997
Corpus ID: 24045862
Tyrosinemia type 3, caused by a genetic deficiency of 4-hydroxyphenylpyruvic acid dioxygenase (HPD) in tyrosine catabolism, is…
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1992
1992
Primary structure deduced from complementary DNA sequence and expression in cultured cells of mammalian 4-hydroxyphenylpyruvic acid dioxygenase. Evidence that the enzyme is a homodimer of identical…
Fumio Endo
,
H. Awata
,
+4 authors
Ichiro Matsuda
Journal of Biological Chemistry
1992
Corpus ID: 22396820
1990
1990
Putative genetic deficiency of 4-hydroxyphenylpyruvic acid dioxygenase in mice: A murine model for hereditary tyrosinaemia type III
F. Endo
,
H. Katoh
,
I. Matsuda
Journal of Inherited Metabolic Disease
1990
Corpus ID: 38457077
Three types of hereditary tyrosinaemia have been described. Type I disease (McKusick 27670) is clinically characterized by liver…
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1979
1979
Conversion of 4‐hydroxyphenylpyruvic acid into homogentisic acid at the thylakoid membrane of Lemna gibba
W. Löffelhardt
,
H. Kindl
FEBS Letters
1979
Corpus ID: 9112471
1979
1979
Metabolism of l-Tyrosine to 4-Hydroxybenzaldehyde and 3-Bromo-4-Hydroxybenzaldehyde by Chloroplast-containing Fractions of Odonthalia floccosa (Esp.) Falk.
S. Manley
,
D. Chapman
Plant Physiology
1979
Corpus ID: 29793312
The biosynthesis of 4-hydroxybenzaldehyde and 3-bromo-4-hydroxybenzaldehyde from l-[U-(14)C]tyrosine has been demonstrated in…
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Highly Cited
1976
Highly Cited
1976
Catabolism of L-tyrosine by the homoprotocatechuate pathway in gram-positive bacteria
V. L. Sparnins
,
P. Chapman
Journal of Bacteriology
1976
Corpus ID: 22303571
A metabolic pathway for L-tyrosine catabolism involves 3,4-dihydroxyphenylacetic acid (homoprotocatechuic acid) as substrate for…
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1975
1975
Occurrence of 4-hydroxyphenylpyruvic acid oxime in the marine spongeHymeniacidon sanguinea
G. Cimino
,
S. D. Stefano
,
L. Minale
Experientia
1975
Corpus ID: 35345892
The occurrence from a marine sponge of 4-hydroxyphenylpyruvic acid oxime is good evidence that an oxime (4) is the biogenetic…
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