These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 173062)

  • 1. Studies on the molecular defect in galactosemia.
    Tedesco TA
    UCLA Forum Med Sci; 1975; (18):467-77. PubMed ID: 173062
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Biochemical mechanisms of the development of hereditary galactosemia in W/SSM strain rats].
    Solov'eva NA; Salganik RI
    Genetika; 1982 Mar; 18(3):420-7. PubMed ID: 7200438
    [TBL] [Abstract][Full Text] [Related]  

  • 3. THE ASSAY OF GALACTOKINASE AND GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE ACTIVITY IN HUMAN ERYTHROCYTES. A PRESUMED TEST FOR HETEROZYGOUS CARRIERS OF THE GALACTOSEMIC DEFECT.
    ROBINSON A
    J Exp Med; 1963 Sep; 118(3):359-70. PubMed ID: 14077997
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Galactosemia: alterations in sulfate metabolism secondary to galactose-1-phosphate uridyltransferase deficiency.
    Tedesco TA; Miller KL
    Science; 1979 Sep; 205(4413):1395-7. PubMed ID: 472754
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Galactose and glucose metabolism in galactokinase deficient, galactose-1-P-uridyl transferase deficient and normal human fibroblasts.
    Friedman TB; Yarkin RJ; Merril CR
    J Cell Physiol; 1975 Jun; 85(3):569-78. PubMed ID: 167035
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Abnormal galactosylation of complex carbohydrates in cultured fibroblasts from patients with galactose-1-phosphate uridyltransferase deficiency.
    Ornstein KS; McGuire EJ; Berry GT; Roth S; Segal S
    Pediatr Res; 1992 May; 31(5):508-11. PubMed ID: 1603629
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis of galactosemia.
    Ng WG; Donnell GN; Bergren WR; Alfi O; Golbus MS
    Clin Chim Acta; 1977 Feb; 74(3):227-35. PubMed ID: 188570
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Problems in the diagnosis of transferase and galactokinase deficient galactosemia.
    Pesce MA; Bodourian SH
    Ann Clin Lab Sci; 1980; 10(1):26-32. PubMed ID: 7362195
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular basis of disorders of human galactose metabolism: past, present, and future.
    Novelli G; Reichardt JK
    Mol Genet Metab; 2000; 71(1-2):62-5. PubMed ID: 11001796
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Transferase-deficiency galactosemia: immunochemical studies of the Duarte and Los Angeles variants.
    Andersen MW; Williams VP; Sparkes MC; Sparkes RS
    Hum Genet; 1984; 65(3):287-90. PubMed ID: 6321325
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Hereditary galactosemia in rats: biochemical mechanisms of the disease].
    Solov'eva NA; Kandaurov VA; Zaĭdman AM; Salganik RI
    Vopr Med Khim; 1982; 28(3):15-21. PubMed ID: 6213094
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rare cases of galactose metabolic disorders: identification of more than two mutations per patient.
    Schulpis KH; Thodi G; Chatzidaki M; Iakovou K; Molou E; Dotsikas Y; Loukas YL
    J Pediatr Endocrinol Metab; 2017 Oct; 30(10):1119-1120. PubMed ID: 28902631
    [No Abstract]   [Full Text] [Related]  

  • 13. [Galactosemia: a problem still unsolved].
    Szczypka M
    Pediatr Pol; 1996 Jun; 71(6):487-92. PubMed ID: 8756765
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Galactosemia].
    Owada M
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):647-51. PubMed ID: 3270877
    [No Abstract]   [Full Text] [Related]  

  • 15. [Correction of the symptoms of hereditary galactosemia in W/SSM strain rats by enzymatic imprinting].
    Salganik RI; Solov'eva NA; Kandaurov VV
    Genetika; 1982 Mar; 18(3):428-33. PubMed ID: 7200439
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Galactosemia. Repository identification Nos. GM-438 to GM-442.
    Kaffe S; Beratis NG; Hirschhorn K; Greene AE; Coriell LL
    Cytogenet Cell Genet; 1976; 17(1):62-4. PubMed ID: 181209
    [No Abstract]   [Full Text] [Related]  

  • 17. Rennes-like variant of galactosemia: clinical and biochemical studies.
    Hammersen G; Houghton S; Levy HL
    J Pediatr; 1975 Jul; 87(1):50-57. PubMed ID: 1151546
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Galactose-1-phosphate uridyltransferase and galactokinase activity in cultured human diploid fibroblasts and peripheral blood leukocytes. I. Analysis of transferase genotypes by the ratio of the activities of the two enzymes.
    Tedesco TA; Mellman WJ
    J Clin Invest; 1969 Dec; 48(12):2390-7. PubMed ID: 5355349
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The activity of galactose-1-phosphate uridyltransferase and galactokinase in human fetal organs.
    Shin-Buehring YS; Beier T; Tan A; Osang M; Schaub J
    Pediatr Res; 1977 Oct; 11(10 Pt 1):1045-51. PubMed ID: 198730
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fluorinated Galactoses Inhibit Galactose-1-Phosphate Uridyltransferase and Metabolically Induce Galactosemia-like Phenotypes in HEK-293 Cells.
    Janes V; Grabany S; Delbrouck J; Vincent SP; Gottschalk J; Elling L; Hanisch FG
    Cells; 2020 Mar; 9(3):. PubMed ID: 32138379
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.