Pages that link to "Q73807435"

The following pages link to Evidence for founder effect of the Glu104Asp substitution and identification of new mutations in triosephosphate isomerase deficiency (Q73807435):

Displaying 19 items.

• Triose phosphate isomerase deficiency is caused by altered dimerization--not catalytic inactivity--of the mutant enzymes (Q21092265) (← links)
• Drosophila model of human inherited triosephosphate isomerase deficiency glycolytic enzymopathy (Q24676326) (← links)
• Crystal structure of triosephosphate isomerase complexed with 2-phosphoglycolate at 0.83-A resolution (Q27640295) (← links)
• The molecular basis of disorders of red cell enzymes (Q33727120) (← links)
• Hsp70- and Hsp90-mediated proteasomal degradation underlies TPIsugarkill pathogenesis in Drosophila (Q34204041) (← links)
• Triosephosphate isomerase I170V alters catalytic site, enhances stability and induces pathology in a Drosophila model of TPI deficiency (Q34714976) (← links)
• The return of metabolism: biochemistry and physiology of the pentose phosphate pathway (Q35752267) (← links)
• Structure and Stability of the Dimeric Triosephosphate Isomerase from the Thermophilic Archaeon Thermoplasma acidophilum (Q35879341) (← links)
• Mechanism for activation of triosephosphate isomerase by phosphite dianion: the role of a hydrophobic clamp (Q36049435) (← links)
• Sequencing and genotypic analysis of the triosephosphate isomerase (TPI1) locus in a large sample of long-lived Germans (Q36713340) (← links)
• Degradation of functional triose phosphate isomerase protein underlies sugarkill pathology (Q36724350) (← links)
• Early mitochondrial dysfunction leads to altered redox chemistry underlying pathogenesis of TPI deficiency (Q36773904) (← links)
• Evidence of a triosephosphate isomerase non-catalytic function crucial to behavior and longevity (Q37012024) (← links)
• Structural analysis on mutation residues and interfacial water molecules for human TIM disease understanding (Q37368236) (← links)
• Inhibition of triosephosphate isomerase by phosphoenolpyruvate in the feedback-regulation of glycolysis (Q37676973) (← links)
• Compensatory role of inducible annexin A2 for impaired biliary epithelial anion-exchange activity of inflammatory cholangiopathy. (Q39788223) (← links)
• Enzyme Architecture: Modeling the Operation of a Hydrophobic Clamp in Catalysis by Triosephosphate Isomerase (Q41246660) (← links)
• Bone marrow transplantation corrects haemolytic anaemia in a novel ENU mutagenesis mouse model of TPI deficiency. (Q55420913) (← links)
• Chronic axonal neuropathy with triosephosphate isomerase deficiency (Q63677348) (← links)