This review briefly discusses the discovery of the mode of action of the triketone herbicide, 2-(2-nitro-4-trifluormethylbenzoyl)-1,3-cyclohexanedione and its use as a drug Nitisinone for the treatment of inborn errors of tyrosine metabolism. Nitisinone is a potent reversible tight-binding inhibitor of the enzyme 4-hydroxyphenylpyruvate dioxygenase, involved in the catabolism of the amino acid tyrosine. Nitisinone is used to treat the rare disease hereditary tyrosinaemia type 1 where the last enzyme in the breakdown of tyrosine, fumarylacetoacetase is deficient. Nitisinone is also used to treat patients with alkaptonuria where the enzyme homogentisic acid oxidase is deficient. Articles in this issue discuss metabolites of tyrosine catabolis...
BackgroundOne of the major metabolic consequences of using nitisinone to treat patients with alkapto...
Introduction: Nitisinone used in alkaptonuria (AKU) can result in keratopathy due to strongly increa...
Abstract Alkaptonuria (AKU, OMIM 203500) is a rare congenital disorder caused by a deficiency of the...
Alkaptonuria (AKU) is a rare multisystem metabolic disease caused by deficient activity of homogenti...
This review mainly focuses on the physiological function of 4-hydroxyphenylpyruvate dioxygenase (HPP...
Introduction: Alkaptonuria is an iconic disease, dating back to the Egyptians and has continued to p...
For over two decades, nitisinone (NTBC) has been successfully used to manipulate the tyrosine degrad...
Nitisinone or 2-(2-nitro-4-trifluoromethylbenzoyl)cyclohexane-1,3-dione, is a reversible inhibitor o...
Changes in the phenylalanine (PHE)/tyrosine (TYR) pathway metabolites before and during homogentisic...
For over two decades, nitisinone (NTBC) has been successfully used to manipulate the tyrosine degrad...
BackgroundAlthough changes in the tyrosine pathway during nitisinone therapy are known, a complete c...
Alkaptonuria (AKU) is an ultra-rare, autosomal recessive disorder of tyrosine catabolism due to muta...
BACKGROUND: Alkaptonuria (AKU) is a serious genetic disease characterised by premature spondyloarth...
Background Alkaptonuria is a rare, debilitating autosomal recessive disorder affecting tyrosine meta...
Metabolomic analyses in alkaptonuria (AKU) have recently revealed alternative pathways in phenylalan...
BackgroundOne of the major metabolic consequences of using nitisinone to treat patients with alkapto...
Introduction: Nitisinone used in alkaptonuria (AKU) can result in keratopathy due to strongly increa...
Abstract Alkaptonuria (AKU, OMIM 203500) is a rare congenital disorder caused by a deficiency of the...
Alkaptonuria (AKU) is a rare multisystem metabolic disease caused by deficient activity of homogenti...
This review mainly focuses on the physiological function of 4-hydroxyphenylpyruvate dioxygenase (HPP...
Introduction: Alkaptonuria is an iconic disease, dating back to the Egyptians and has continued to p...
For over two decades, nitisinone (NTBC) has been successfully used to manipulate the tyrosine degrad...
Nitisinone or 2-(2-nitro-4-trifluoromethylbenzoyl)cyclohexane-1,3-dione, is a reversible inhibitor o...
Changes in the phenylalanine (PHE)/tyrosine (TYR) pathway metabolites before and during homogentisic...
For over two decades, nitisinone (NTBC) has been successfully used to manipulate the tyrosine degrad...
BackgroundAlthough changes in the tyrosine pathway during nitisinone therapy are known, a complete c...
Alkaptonuria (AKU) is an ultra-rare, autosomal recessive disorder of tyrosine catabolism due to muta...
BACKGROUND: Alkaptonuria (AKU) is a serious genetic disease characterised by premature spondyloarth...
Background Alkaptonuria is a rare, debilitating autosomal recessive disorder affecting tyrosine meta...
Metabolomic analyses in alkaptonuria (AKU) have recently revealed alternative pathways in phenylalan...
BackgroundOne of the major metabolic consequences of using nitisinone to treat patients with alkapto...
Introduction: Nitisinone used in alkaptonuria (AKU) can result in keratopathy due to strongly increa...
Abstract Alkaptonuria (AKU, OMIM 203500) is a rare congenital disorder caused by a deficiency of the...