Tyrosinemia, Type III

Known as: 4 Hydroxyphenol Pyruvic Acid Oxidase Deficiency Disease, Dioxygenase Deficiency, 4-Hydroxyphenylpyruvate, Deficiency, 4-Hydroxyphenylpyruvate Dioxygenase 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1952-2017
0519522016

Papers overview

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2016
2016
Tet methylcytosine dioxygenase 2 (TET2) mediates the conversion of 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC). The… (More)
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2015
2015
Tyrosinemia type 3 (HT3) is a rare inborn error of tyrosine metabolism caused by mutations in the HPD gene encoding 4… (More)
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Highly Cited
2012
Highly Cited
2012
The modification of DNA by 5-methylcytosine (5mC) has essential roles in cell differentiation and development through epigenetic… (More)
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2011
2011
Heterotrimeric G protein complexes are conserved from plants to mammals, but the complexity of each system varies. Arabidopsis… (More)
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2007
2007
We have previously identified an androgen-responsive gene in rat prostate that shares homology with the aci-reductone dioxygenase… (More)
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2005
2005
Carbazole 1,9a-dioxygenase (CARDO) catalyzes the dihydroxylation of carbazole by angular position (C9a) carbon bonding to the… (More)
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2004
2004
(4-Hydroxyphenyl)pyruvate dioxygenase (HPPD) is an unusual alpha-keto acid-dependent non-heme iron dioxygenase as it incorporates… (More)
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2000
2000
The TcmG or ElmG oxygenase-catalyzed triple hydroxylation of tetracenomycin (Tcm) A2 to Tcm C proceeds via a novel monooxygenase… (More)
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1999
1999
  • K Lee
  • Journal of bacteriology
  • 1999
Naphthalene dioxygenase (NDO) is a multicomponent enzyme system that oxidizes naphthalene to (+)-cis-(1R,2S)-1,2-dihydroxy-1, 2… (More)
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1997
1997
Tyrosinemia type III, caused by deficiency of 4-hydroxyphenylpyruvate dioxygenase, is a rare disorder of tyrosine catabolism… (More)
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