BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 203421)

  • 21. Electrophoretic abnormality of galactose-1-phosphate uridyl transferase in galactosemia.
    Schapira F; Kaplan JC
    Biochem Biophys Res Commun; 1969 May; 35(4):451-5. PubMed ID: 5788501
    [No Abstract]   [Full Text] [Related]  

  • 22. Presenile cataract formation and decreased activity of galactosemic enzymes.
    Skalka HW; Prchal JT
    Arch Ophthalmol; 1980 Feb; 98(2):269-73. PubMed ID: 7352874
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Biokinetics of galactose in the homozygotes and heterozygotes of both forms of galactosemia.
    Sitzmann FC; Kaloud H
    Clin Chim Acta; 1976 Nov; 72(3):343-51. PubMed ID: 184990
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Human erythrocyte galactokinase and galactose-1-phosphate uridylyltransferase: a population survey.
    Tedesco TA; Miller KL; Rawnsley BE; Mennuti MT; Spielman RS; Mellman WJ
    Am J Hum Genet; 1975 Nov; 27(6):737-47. PubMed ID: 173184
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Pathological findings in galactosemia caused by a galactose-1-phosphaturidyltransferase defect (author's transl)].
    Gathmann HA
    Klin Padiatr; 1977 Mar; 189(2):177-84. PubMed ID: 558474
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Comparison of galactose-1-phosphate uridyl transferase in fetal and adult tissues.
    Hammersen G; Levy HL; Frigoletto F; Mandell R
    Clin Chim Acta; 1975 May; 60(3):281-4. PubMed ID: 1139775
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal diagnosis of galactosemia and properties of galactose-1-phosphate uridyltransferase in erythrocytes of galactosemic variants as well as in human fetal and adult organs.
    Shin YS; Endres W; Rieth M; Schaub J
    Clin Chim Acta; 1983 Mar; 128(2-3):271-81. PubMed ID: 6303628
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Galactosemia as a result of galactose-1-phosphate uridyltransferase deficiency.
    Vaca G; Sanchez-Corona J; Medina C; Olivares N; Rivera H; Hernández A; Ibarra B; Sotomayor JM; Cantú JM
    Arch Invest Med (Mex); 1978; 9(3):477-84. PubMed ID: 568459
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Falsely normal value in fluorometric transferase screening of galactosemic blood. A cautionary note.
    Beutler E; Gelbart T
    Am J Clin Pathol; 1981 Dec; 76(6):841-2. PubMed ID: 6274187
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Preliminary results of UDP galactose pyrophosphorylase in the erythrocytes of healthy persons and in patients with galactosaemia.
    Mańkowski T; Radomyska B; Zbieg-Sendecka E
    Mater Med Pol; 1990; 22(3):191-3. PubMed ID: 2132425
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular analysis of 11 galactosemia patients.
    Reichardt JK
    Nucleic Acids Res; 1991 Dec; 19(25):7049-52. PubMed ID: 1766867
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Galactose-1-phosphate uridyl transferase deficiency due to Duarte/galactosemia combined variation: clinical and biochemical studies.
    Levy HL; Sepe SJ; Walton DS; Shih VE; Hammersen G; Houghton S; Beutler E
    J Pediatr; 1978 Mar; 92(3):390-3. PubMed ID: 632977
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Galactose-1-phosphate uridyl transferase in fibroblasts: isozymes in normal and variant states.
    Hammersen G; Mandell R; Levy HL
    Ann Hum Genet; 1975 Oct; 39(2):147-50. PubMed ID: 1052762
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [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]  

  • 37. Loss of transferase enzyme activity of transfused erythrocytes in galactosemia.
    Schwartz RP; Roesel RA; Blankenship PR; Hall WK
    South Med J; 1975 Mar; 68(3):301-2. PubMed ID: 1118770
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Radiochemical assay of minute quantities of galactose-1-phosphate uridyltransferase activity in erythrocytes and leukocytes of galactosemia patients.
    Xu YK; Kaufman FR; Donnell GN; Ng WG
    Clin Chim Acta; 1995 Mar; 235(2):125-36. PubMed ID: 7554267
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Galactose intolerance in individuals with double heterozygosity for Duarte variant and galactosemia.
    Schwarz HP; Zuppinger KA; Zimmerman A; Dauwalder H; Scherz R; Bier DM
    J Pediatr; 1982 May; 100(5):704-9. PubMed ID: 7069531
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Letter: Localisation of human gene for galactose-1-phosphate-uridyltransferase.
    Allerdice PW; Tedesco TA
    Lancet; 1975 Jul; 2(7923):39. PubMed ID: 49636
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.