Increased formation of methylglyoxal and protein glycation, oxidation and nitrosation in triosephosphate isomerase deficiency

Author:

Ahmed Naila,Battah Sinan,Karachalias Nikolaos,Babaei-Jadidi Roya,Horányi Margit,Baróti Klára,Hollan Susan,Thornalley Paul J.

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference34 articles.

1. Triosephosphate isomerase deficiency: historical perspectives and molecular aspects;Schneider;Bailliere's Clin. Haematol.,2000

2. Human triose-phosphate isomerase deficiency: a single amino acid substitution results in a thermolabile enzyme;Daar;Proc. Natl. Acad. Sci. U. S. A.,1986

3. Human triosephosphate isomerase deficiency resulting from mutations of the Phe-240;Chang;Am. J. Hum. Genet.,1993

4. Identical germ-line mutations in the triosephosphate isomerase alleles of two brothers are associated with distinct clinical phenotypes;Valentin;Life Sci.,2000

5. Hereditary triosephosphate isomerase (TPI) deficiency: two severely affected brothers one with and one without neurological problems;Hollan;Hum. Genet.,1993

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