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Journal Abstract Search
144 related items for PubMed ID: 7488826
41. 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 15; 340 ( Pt 1)(Pt 1):321-7. PubMed ID: 10229688 [Abstract] [Full Text] [Related]
50. 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 Mar 26; 7(4):409-14. PubMed ID: 10352930 [Abstract] [Full Text] [Related]
51. Allelic heterogeneity in adult hereditary fructose intolerance. Detection of structural mutations in the aldolase B molecule. Cox TM, O'Donnell MW, Camilleri M. Mol Biol Med; 1983 Nov 26; 1(4):393-400. PubMed ID: 6680153 [Abstract] [Full Text] [Related]
52. DNA analysis in patients with hereditary fructose intolerance. Grégori C, Besmond C, Odievre M, Kahn A, Dreyfus JC. Ann Hum Genet; 1984 Oct 26; 48(4):291-6. PubMed ID: 6093679 [Abstract] [Full Text] [Related]
53. Stabilization of the predominant disease-causing aldolase variant (A149P) with zwitterionic osmolytes. Stopa JD, Chandani S, Tolan DR. Biochemistry; 2011 Feb 08; 50(5):663-71. PubMed ID: 21166391 [Abstract] [Full Text] [Related]
56. [Hereditary fructose intolerance]. Lopes AI, Almeida AG, Costa AE, Costa A, Leite M. Acta Med Port; 1998 Dec 08; 11(12):1121-5. PubMed ID: 10192989 [Abstract] [Full Text] [Related]
57. Increased prevalence of mutant null alleles that cause hereditary fructose intolerance in the American population. Coffee EM, Yerkes L, Ewen EP, Zee T, Tolan DR. J Inherit Metab Dis; 2010 Feb 08; 33(1):33-42. PubMed ID: 20033295 [Abstract] [Full Text] [Related]