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182 related items for PubMed ID: 4212946
1. Antibody activation of mutant human fructosediphosphate aldolase B in liver extracts of patients with hereditary fructose intolerance. Gitzelmann R, Steinmann B, Bally C, Lebherz HG. Biochem Biophys Res Commun; 1974 Aug 19; 59(4):1270-7. PubMed ID: 4212946 [No Abstract] [Full Text] [Related]
2. 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 19; 72(1):201-13. PubMed ID: 6348085 [Abstract] [Full Text] [Related]
3. Isoelectrofocusing of aldolase B from normal human livers and from livers with hereditary fructose intolerance. Schapira F, Gregori C, Hatzfeld A. Clin Chim Acta; 1977 Jul 01; 78(1):1-8. PubMed ID: 884843 [Abstract] [Full Text] [Related]
4. Kinetic and immunological abnormalities of aldolase B in herediatry fructose intolerance. Schapira F. Biochem Soc Trans; 1975 Jul 01; 3(2):232-4. PubMed ID: 805723 [No Abstract] [Full Text] [Related]
5. Possible role of thiol groups in the abnormal kinetics of aldolase in hereditary fructose intolerance. Lemonnier F, Gregori C, Schapira F. Biochem Biophys Res Commun; 1974 Nov 06; 61(1):306-12. PubMed ID: 4441399 [No Abstract] [Full Text] [Related]
6. Structural mutation of aldolase B in hereditary fructose intolerance: electrofocusing results. Schapira F, Hatzfeld A, Gregori C. Monogr Hum Genet; 1978 Nov 06; 9():2-6. PubMed ID: 732841 [No Abstract] [Full Text] [Related]
7. Studies on liver aldolases in hereditary fructose intolerance. Schapira F, Hatzfeld A, Gregori C. Enzyme; 1974 Nov 06; 18(1):73-83. PubMed ID: 4212363 [No Abstract] [Full Text] [Related]
8. On the biochemical basis of hereditary fructose intolerance. Koster JF, Slee RG, Fernandes J. Biochem Biophys Res Commun; 1975 May 05; 64(1):289-94. PubMed ID: 1147924 [No Abstract] [Full Text] [Related]
9. Aldolase activities of the small intestinal mucosa in malabsorption states and hereditary fructose intolerance. Streb H, Posselt HG, Wolter K, Bender SW. Eur J Pediatr; 1981 Sep 05; 137(1):5-10. PubMed ID: 7274301 [No Abstract] [Full Text] [Related]
10. Molecular studies of liver aldolase B in hereditary fructose intolerance using blotting and immunological techniques. Grégori C, Schapira F, Kahn A, Delpech M, Dreyfus JC. Ann Hum Genet; 1982 Oct 05; 46(4):281-92. PubMed ID: 6760789 [Abstract] [Full Text] [Related]
11. [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 Oct 05; 136(6):456-8. PubMed ID: 3841265 [Abstract] [Full Text] [Related]
13. Fructose intolerance with normal liver aldolase. Corbeel LM, Eggermont E, Bettens W, Casteels-Van Daele M, Timmermans J. Helv Paediatr Acta; 1970 Dec 05; 25(6):626-33. PubMed ID: 5515944 [No Abstract] [Full Text] [Related]
14. Fructose-1-phosphate aldolase and fructose-1-6-diphosphate aldolase activity in the mucosa of the intestine in hereditary fructose intolerance. Nisell J, Lindén L. Scand J Gastroenterol; 1968 Dec 05; 3(1):80-2. PubMed ID: 5655259 [No Abstract] [Full Text] [Related]
15. [Hereditary fructose intolerance. Description of a clinical case with verified enzyme deficiency]. Cardi E, D'Eufemia P, Gambarara M, Cieri E, Giardini O. Minerva Pediatr; 1979 Dec 31; 31(24):1781-6. PubMed ID: 550065 [No Abstract] [Full Text] [Related]
16. Aldocase activities in the liver in parents of patients with hereditary fructose intolerance. Raivio K, Perheentupa J, Nikkilä EA. Clin Chim Acta; 1967 Aug 31; 17(2):275-9. PubMed ID: 6035549 [No Abstract] [Full Text] [Related]
17. A radioisotopic method for fructose-1-phosphate aldolase assay that facilitates diagnosis of hereditary fructose intolerance. Shin YS, Moro V, Doliwa H, Endres W. Clin Chem; 1983 Nov 31; 29(11):1955-8. PubMed ID: 6627633 [Abstract] [Full Text] [Related]
18. [Liver fructose-1-phosphate and fructose-1,6-diphosphate aldolase deficiency in hereditary fructose intolerance (author's transl)]. Joosten R, Berzdorf M, de Barsy T, Habedank M. Klin Padiatr; 1981 Sep 31; 193(5):392-3. PubMed ID: 7289434 [No Abstract] [Full Text] [Related]
19. 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 17; 53(6):881-5. PubMed ID: 3383242 [Abstract] [Full Text] [Related]
20. Pseudodominant transmission of fructose intolerance in an adult and three offspring: Heterozygote detection by intestinal biopsy. Cox TM, Camilleri M, O'Donnell MW, Chadwick VS. N Engl J Med; 1982 Aug 26; 307(9):537-40. PubMed ID: 7099225 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]