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 *

137 related articles for article (PubMed ID: 962903)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Polymorphism of erythrocyte galactose-1-phosphate uridyl-transferase in Italy: segregation analysis in 693 families.
    Vaccaro AM; Mandara I; Muscillo M; Ciaffoni F; De Pellegrin S; Benincasa A; Novelletto A; Terrenato L
    Hum Hered; 1984; 34(4):197-206. PubMed ID: 6090305
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Isoelectrofocusing of erythrocyte galactose 1 phospho uridyl transferase in a family with both galactosemia and Duarte variants.
    Schapira F; Gregori C; Banroques J; Vidailhet M; Despoisses S; Vigneron C
    Hum Genet; 1979 Jan; 46(1):89-96. PubMed ID: 429011
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Enzymatic micromethod for measuring galactose-1-phosphate uridylyltransferase activity in human erythrocytes.
    Pesce MA; Bodourian SH; Harris RC; Nicholson JF
    Clin Chem; 1977 Sep; 23(9):1711-7. PubMed ID: 890916
    [No Abstract]   [Full Text] [Related]  

  • 10. Study of a family with both galactosemic and Duarte variants of galactose-1-phospho uridyl transferase.
    Schapira F; Gregori C; Poenaru L
    Biochem Med; 1974 Sep; 11(1):87-92. PubMed ID: 4415964
    [No Abstract]   [Full Text] [Related]  

  • 11. [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]  

  • 12. [Galactosemia and cow's milk intolerance (author's transl)].
    Gómez de Terreros I; Gayoso Gómez F; Senín Sánchez J; Castro Gómez A; Muñóz Conde J; de la Rosa A
    An Esp Pediatr; 1978 Feb; 11(2):157-64. PubMed ID: 655510
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Determination of galactose-1-phosphate-uridyl-transferase activity in children with galactosemia and their relatives].
    Knapp W; Winkler G
    Padiatr Grenzgeb; 1972; 11(1):35-47. PubMed ID: 5042112
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Reagent that restores galactose-1-phosphate uridylyltransferase activity in dry blood spots.
    Berry HK; Croft CC
    Clin Chem; 1987 Aug; 33(8):1471-2. PubMed ID: 3038378
    [No Abstract]   [Full Text] [Related]  

  • 18. The Chicago variant of clinical galactosemia.
    Chacko CM; Wappner RS; Brandt IK; Nadler HL
    Hum Genet; 1977 Jul; 37(3):261-70. PubMed ID: 885545
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.