This project describes a drug discovery plan for Classic Galactosemia, a rare disorder of galactose metabolism where there is currently no disease-transforming therapy. This TEP provides the protein reagents, biophysical assays, and structural information to facilitate two aspects of galactosemia research: (i) to understand the molecular basis of the disease due to defective GALT enzyme, and (ii) to provide chemical starting points to explore metabolic intervention of the upstream enzyme GALK1 aimed at mitigating the GALT defect (substrate reduction).This document represents version 2 of the TEP datasheet and includes all updates on the project as of June 2019. For more information about TEPs and the TEP Programme, please visit https://thes...
Classic galactosemia is an autosomal recessive disorder caused by deleterious variants in the galact...
Hereditary galactosemia is an inborn error of carbohydrate metabolism. Galactose is metabolized by L...
Classic Galactosemia (CG) is an autosomal recessive disorder caused by deleterious mutations of gala...
This project describes a drug discovery plan for Classic Galactosemia, a rare disorder of galactose ...
This project describes a drug discovery plan for Classic Galactosemia, a rare disorder of galactose ...
This project describes a drug discovery plan for Classic Galactosemia, a rare disorder of galactose ...
Galactosemia is an inherited metabolic disease affecting enzymes of the Leloir pathway of galactose ...
Reduced galactose 1-phosphate uridylyltransferase (GALT) activity is associated with the genetic dis...
Type I galactosemia is a genetic disorder that is caused by the impairment of galactose-1-phosphate ...
AbstractType I galactosemia is a genetic disorder that is caused by the impairment of galactose-1-ph...
Type I (classic) galactosemia, galactose 1-phosphate uridylyltransferase (GALT)-deficiency is a here...
Type I galactosemia results from reduced galactose 1-phosphate uridylyltransferase (GALT) activity. ...
Type I galactosemia results from reduced galactose 1-phosphate uridylyltransferase (GALT) activity. ...
The purpose of this project was to find inhibitors of the human galactokinase (GALK) enzyme. GALK is...
Galactosemia, an inborn error of galactose metabolism, was first described in the 1900s by von Ruess...
Classic galactosemia is an autosomal recessive disorder caused by deleterious variants in the galact...
Hereditary galactosemia is an inborn error of carbohydrate metabolism. Galactose is metabolized by L...
Classic Galactosemia (CG) is an autosomal recessive disorder caused by deleterious mutations of gala...
This project describes a drug discovery plan for Classic Galactosemia, a rare disorder of galactose ...
This project describes a drug discovery plan for Classic Galactosemia, a rare disorder of galactose ...
This project describes a drug discovery plan for Classic Galactosemia, a rare disorder of galactose ...
Galactosemia is an inherited metabolic disease affecting enzymes of the Leloir pathway of galactose ...
Reduced galactose 1-phosphate uridylyltransferase (GALT) activity is associated with the genetic dis...
Type I galactosemia is a genetic disorder that is caused by the impairment of galactose-1-phosphate ...
AbstractType I galactosemia is a genetic disorder that is caused by the impairment of galactose-1-ph...
Type I (classic) galactosemia, galactose 1-phosphate uridylyltransferase (GALT)-deficiency is a here...
Type I galactosemia results from reduced galactose 1-phosphate uridylyltransferase (GALT) activity. ...
Type I galactosemia results from reduced galactose 1-phosphate uridylyltransferase (GALT) activity. ...
The purpose of this project was to find inhibitors of the human galactokinase (GALK) enzyme. GALK is...
Galactosemia, an inborn error of galactose metabolism, was first described in the 1900s by von Ruess...
Classic galactosemia is an autosomal recessive disorder caused by deleterious variants in the galact...
Hereditary galactosemia is an inborn error of carbohydrate metabolism. Galactose is metabolized by L...
Classic Galactosemia (CG) is an autosomal recessive disorder caused by deleterious mutations of gala...