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7. Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation. Cross NC; Tolan DR; Cox TM Cell; 1988 Jun; 53(6):881-5. PubMed ID: 3383242 [TBL] [Abstract][Full Text] [Related]
8. Alteration of substrate specificity by a naturally-occurring aldolase B mutation (Ala337-->Val) in fructose intolerance. Rellos P; Ali M; Vidailhet M; Sygusch J; Cox TM Biochem J; 1999 May; 340 ( Pt 1)(Pt 1):321-7. PubMed ID: 10229688 [TBL] [Abstract][Full Text] [Related]
9. A newly identified aldolase B splicing mutation (G-->C, 5' intron 5) in hereditary fructose intolerance from New Zealand. Ali M; James CL; Cox TM Hum Mutat; 1996; 7(2):155-7. PubMed ID: 8829634 [No Abstract] [Full Text] [Related]
10. Hereditary fructose intolerance. Wong D Mol Genet Metab; 2005 Jul; 85(3):165-7. PubMed ID: 16086449 [No Abstract] [Full Text] [Related]
11. Case report: heterogeneity of aldolase B in hereditary fructose intolerance. Kaiser UB; Hegele RA Am J Med Sci; 1991 Dec; 302(6):364-8. PubMed ID: 1772121 [TBL] [Abstract][Full Text] [Related]
12. The temperature dependence of activity and structure for the most prevalent mutant aldolase B associated with hereditary fructose intolerance. Malay AD; Procious SL; Tolan DR Arch Biochem Biophys; 2002 Dec; 408(2):295-304. PubMed ID: 12464284 [TBL] [Abstract][Full Text] [Related]
13. Mutation of aldolase B genes in hereditary fructose intolerance. de Souza M; Lindeman R; Volpato F; Trent RJ; Kamath R Lancet; 1990 Apr; 335(8693):856. PubMed ID: 1969579 [No Abstract] [Full Text] [Related]
14. Identification of a novel mutation (Leu256-->Pro) in the human aldolase B gene associated with hereditary fructose intolerance. Ali M; Sebastio G; Cox TM Hum Mol Genet; 1994 Apr; 3(4):684. PubMed ID: 8069328 [No Abstract] [Full Text] [Related]
15. Partial aldolase B gene deletions in hereditary fructose intolerance. Cross NC; Cox TM Am J Hum Genet; 1990 Jul; 47(1):101-6. PubMed ID: 2349937 [TBL] [Abstract][Full Text] [Related]
16. Molecular analysis of the aldolase B gene in patients with hereditary fructose intolerance from Spain. Sánchez-Gutiérrez JC; Benlloch T; Leal MA; Samper B; García-Ripoll I; Felíu JE J Med Genet; 2002 Sep; 39(9):e56. PubMed ID: 12205126 [No Abstract] [Full Text] [Related]
17. A possible case of transient hereditary fructose intolerance. Catto-Smith AG; Adams A J Inherit Metab Dis; 1993; 16(1):73-7. PubMed ID: 8487506 [TBL] [Abstract][Full Text] [Related]
18. 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 [TBL] [Abstract][Full Text] [Related]
19. Activation of AMPD2 drives metabolic dysregulation and liver disease in mice with hereditary fructose intolerance. Andres-Hernando A; Orlicky DJ; Kuwabara M; Fini MA; Tolan DR; Johnson RJ; Lanaspa MA Commun Biol; 2024 Jul; 7(1):849. PubMed ID: 38992061 [TBL] [Abstract][Full Text] [Related]
20. [Study of hereditary fructose intolerance by methods of molecular biology]. Dreyfus JC; Schapira F; Besmond C; Gregori C; Kahn A Ann Med Interne (Paris); 1985; 136(6):456-8. PubMed ID: 3841265 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]