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PUBMED FOR HANDHELDS

Journal Abstract Search


208 related items for PubMed ID: 7832803

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  • 4. Novel six-nucleotide deletion in the hepatic fructose-1,6-bisphosphate aldolase gene in a patient with hereditary fructose intolerance and enzyme structure-function implications.
    Santamaria R, Vitagliano L, Tamasi S, Izzo P, Zancan L, Zagari A, Salvatore F.
    Eur J Hum Genet; 1999; 7(4):409-14. PubMed ID: 10352930
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  • 6. Molecular cloning, expression, purification, and characterization of fructose 1,6-bisphosphate aldolase from Mycobacterium tuberculosis--a novel Class II A tetramer.
    Ramsaywak PC, Labbé G, Siemann S, Dmitrienko GI, Guillemette JG.
    Protein Expr Purif; 2004 Sep; 37(1):220-8. PubMed ID: 15294302
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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
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  • 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
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  • 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
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  • 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
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  • 16. Human sphingosine kinase: purification, molecular cloning and characterization of the native and recombinant enzymes.
    Pitson SM, D'andrea RJ, Vandeleur L, Moretti PA, Xia P, Gamble JR, Vadas MA, Wattenberg BW.
    Biochem J; 2000 Sep 01; 350 Pt 2(Pt 2):429-41. PubMed ID: 10947957
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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
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  • 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
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