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26. Expression, purification, and characterization of natural mutants of human aldolase B. Role of quaternary structure in catalysis. Rellos P; Sygusch J; Cox TM J Biol Chem; 2000 Jan; 275(2):1145-51. PubMed ID: 10625657 [TBL] [Abstract][Full Text] [Related]
27. Molecular analysis of aldolase B genes in hereditary fructose intolerance. Cross NC; de Franchis R; Sebastio G; Dazzo C; Tolan DR; Gregori C; Odievre M; Vidailhet M; Romano V; Mascali G Lancet; 1990 Feb; 335(8685):306-9. PubMed ID: 1967768 [TBL] [Abstract][Full Text] [Related]
28. Molecular analysis of common aldolase B alleles for hereditary fructose intolerance in North Americans. Tolan DR; Brooks CC Biochem Med Metab Biol; 1992 Aug; 48(1):19-25. PubMed ID: 1524867 [TBL] [Abstract][Full Text] [Related]
29. A functional role for a flexible loop containing Glu182 in the class II fructose-1,6-bisphosphate aldolase from Escherichia coli. Zgiby S; Plater AR; Bates MA; Thomson GJ; Berry A J Mol Biol; 2002 Jan; 315(2):131-40. PubMed ID: 11779234 [TBL] [Abstract][Full Text] [Related]
30. Exploring substrate binding and discrimination in fructose1, 6-bisphosphate and tagatose 1,6-bisphosphate aldolases. Zgiby SM; Thomson GJ; Qamar S; Berry A Eur J Biochem; 2000 Mar; 267(6):1858-68. PubMed ID: 10712619 [TBL] [Abstract][Full Text] [Related]
31. Characterization of recombinant human aldolase B and purification by metal chelate chromatography. Doyle SA; Tolan DR Biochem Biophys Res Commun; 1995 Jan; 206(3):902-8. PubMed ID: 7832803 [TBL] [Abstract][Full Text] [Related]
32. [Congenital fructose intolerance. New molecular aspects]. Larsen K; Adnanes O; Aarskog NK; Runde I; Ogreid D Tidsskr Nor Laegeforen; 1994 Nov; 114(28):3312-4. PubMed ID: 7809888 [TBL] [Abstract][Full Text] [Related]
33. Aldolase B mutations and prevalence of hereditary fructose intolerance in a Polish population. Gruchota J; Pronicka E; Korniszewski L; Stolarski B; Pollak A; Rogaszewska M; Płoski R Mol Genet Metab; 2006 Apr; 87(4):376-8. PubMed ID: 16406649 [TBL] [Abstract][Full Text] [Related]
34. Subunit interface mutants of rabbit muscle aldolase form active dimers. Beernink PT; Tolan DR Protein Sci; 1994 Sep; 3(9):1383-91. PubMed ID: 7833800 [TBL] [Abstract][Full Text] [Related]
36. Molecular basis of hereditary fructose intolerance in Italy: identification of two novel mutations in the aldolase B gene. Santamaria R; Tamasi S; Del Piano G; Sebastio G; Andria G; Borrone C; Faldella G; Izzo P; Salvatore F J Med Genet; 1996 Sep; 33(9):786-8. PubMed ID: 8880583 [TBL] [Abstract][Full Text] [Related]
37. Molecular basis of hereditary fructose intolerance: mutations and polymorphisms in the human aldolase B gene. Tolan DR Hum Mutat; 1995; 6(3):210-8. PubMed ID: 8535439 [TBL] [Abstract][Full Text] [Related]
38. 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; 268(2):1095-100. PubMed ID: 8419316 [TBL] [Abstract][Full Text] [Related]
39. Aldolase B A149P mutation and hereditary fructose intolerance are not associated with sudden infant death syndrome. Aarskog NK; Ogreid D Acta Paediatr; 1995 Aug; 84(8):947-8. PubMed ID: 7488826 [No Abstract] [Full Text] [Related]
40. 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; 380(Pt 1):51-6. PubMed ID: 14766013 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]