BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 related articles for article (PubMed ID: 14204065)

  • 1. GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE ACTIVITY IN GALACTOSAEMIA.
    WONGIN NG; BERGREN WR; DONNELL GN
    Nature; 1964 Aug; 203():845-7. PubMed ID: 14204065
    [No Abstract]   [Full Text] [Related]  

  • 2. ERYTHROCYTIC GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE LEVELS IN HEPATIC CIRRHOSIS.
    FISHER MM; SPEAR S; SAMOLS E; SHERLOCK S
    Gut; 1964 Apr; 5(2):170-2. PubMed ID: 14159408
    [No 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. 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]  

  • 5. Clinical significance of plasma galactose and erythrocyte galactose-1-phosphate measurements in transferase-deficient galactosemia and in individuals with below-normal transferase activity.
    Pesce MA; Bodourian SH
    Clin Chem; 1982 Feb; 28(2):301-5. PubMed ID: 6276048
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The use of glucose-1-[32P]phosphate for the determination of hexose-1-phosphate uridyl transferase activity in red blood cells.
    Grodzka Z; Chojnacki T
    Biochem Med; 1976 Dec; 16(3):182-6. PubMed ID: 1016259
    [No Abstract]   [Full Text] [Related]  

  • 7. [Galactose 1-phosphate level in children with various types of hexosephosphate uridylyltransferase deficiency].
    Grodzka Z; Zbieg-Sendecka E; Mańkowski T
    Pediatr Pol; 1985 Sep; 60(9):631-7. PubMed ID: 3008074
    [No Abstract]   [Full Text] [Related]  

  • 8. Biochemical studies of a human low-activity galactose-1-phosphate uridyl transferase variant.
    Ng WG; Kline F; Lin J; Koch R; Donnell GN
    J Inherit Metab Dis; 1978; 1(4):145-51. PubMed ID: 117249
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Clinical and biochemical diagnosis of galactosemia among our cases].
    Bozkowa K; Zbieg-Sendecka E; Grodzka Z; Cabalska B
    Probl Med Wieku Rozwoj; 1979; 8():63-9. PubMed ID: 263527
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Galactose-1-phosphate uridyl transferase activity in haemolysate mixtures.
    BERGREN WR; DONNELL GN
    Ann Hum Genet; 1962 Nov; 26():135-6. PubMed ID: 13970785
    [No Abstract]   [Full Text] [Related]  

  • 11. Study of a family with Los Angeles, Duarte, and classical galactosemia variants of galactose-1-phosphate uridyl transferase.
    Applegarth DA; Donnell GN; Mullinger M; Ng WG; Lowry AB
    Biochem Med; 1976 Apr; 15(2):206-11. PubMed ID: 962903
    [No Abstract]   [Full Text] [Related]  

  • 12. Pitfalls in the radioactive method of galactose-1-phosphate uridyltransferase activity measurement.
    Shin-Buehring YS; Schaub J
    Clin Chim Acta; 1980 Sep; 106(2):231-4. PubMed ID: 6250747
    [No Abstract]   [Full Text] [Related]  

  • 13. GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE ASSAY BY USE OF RADIOACTIVE GALACTOSE-1-PHOSPHATE.
    NG WG; BERGEN WR; DONNELL GN
    Clin Chim Acta; 1964 Oct; 10():337-43. PubMed ID: 14219578
    [No Abstract]   [Full Text] [Related]  

  • 14. [Double heterozygosity (transferase-/epimerase-defect) and galactosemia cataract].
    Heyne K; Shin YS; Schwinger E
    Monatsschr Kinderheilkd; 1988 Dec; 136(12):828-30. PubMed ID: 2853298
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Correlation of ovarian function with galactose-1-phosphate uridyl transferase levels in galactosemia.
    Kaufman FR; Xu YK; Ng WG; Donnell GN
    J Pediatr; 1988 May; 112(5):754-6. PubMed ID: 2834527
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. A screening procedure and a specific quantitative method for UDPglucose: alpha-D-galactose-1-phosphate uridylyltransferase (EC 2.7.7.12).
    Ibbott FA
    Clin Chem; 1977 Jul; 23(7):1348-55. PubMed ID: 872388
    [No Abstract]   [Full Text] [Related]  

  • 19. Prenatal and postnatal diagnostic difficulties in a family with rare alleles of the galactose-1-phosphate uridyl transferase locus.
    Christensen E; Brandt NJ
    J Inherit Metab Dis; 1978; 1(4):167-9. PubMed ID: 117252
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A mouse model of galactose-1-phosphate uridyl transferase deficiency.
    Leslie ND; Yager KL; McNamara PD; Segal S
    Biochem Mol Med; 1996 Oct; 59(1):7-12. PubMed ID: 8902187
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.