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10. Isolation and characterization of a mutant liver aldolase in adult hereditary fructose intolerance. Identification of the enzyme variant by radioassay in tissue biopsy specimens. Cox TM, O'Donnell MW, Camilleri M, Burghes AH. J Clin Invest; 1983 Jul; 72(1):201-13. PubMed ID: 6348085 [Abstract] [Full Text] [Related]
11. Mechanism of the Schiff base forming fructose-1,6-bisphosphate aldolase: structural analysis of reaction intermediates. Lorentzen E, Siebers B, Hensel R, Pohl E. Biochemistry; 2005 Mar 22; 44(11):4222-9. PubMed ID: 15766250 [Abstract] [Full Text] [Related]
12. Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme function. Esposito G, Vitagliano L, Costanzo P, Borrelli L, Barone R, Pavone L, Izzo P, Zagari A, Salvatore F. Biochem J; 2004 May 15; 380(Pt 1):51-6. PubMed ID: 14766013 [Abstract] [Full Text] [Related]
13. Caenorhabditis elegans has two isozymic forms, CE-1 and CE-2, of fructose-1,6-bisphosphate aldolase which are encoded by different genes. Inoue T, Yatsuki H, Kusakabe T, Joh K, Takasaki Y, Nikoh N, Miyata T, Hori K. Arch Biochem Biophys; 1997 Mar 01; 339(1):226-34. PubMed ID: 9056253 [Abstract] [Full Text] [Related]
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17. Starvation-induced lysosomal degradation of aldolase B requires glutamine 111 in a signal sequence for chaperone-mediated transport. Susan PP, Dunn WA. J Cell Physiol; 2001 Apr 01; 187(1):48-58. PubMed ID: 11241348 [Abstract] [Full Text] [Related]
18. Site-directed mutagenesis identifies aspartate 33 as a previously unidentified critical residue in the catalytic mechanism of rabbit aldolase A. Morris AJ, Tolan DR. J Biol Chem; 1993 Jan 15; 268(2):1095-100. PubMed ID: 8419316 [Abstract] [Full Text] [Related]