BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

84 related articles for article (PubMed ID: 1166519)

  • 1. [Stimulation of DNA synthesis and mitoses in the rat liver in experimental galactosemia caused by the prolonged administration of galactose].
    Kostyrev OA; Solov'eva NA
    Tsitologiia; 1975 Sep; 17(9):1042-6. PubMed ID: 1166519
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Development of a rat subline with symptoms of hereditary galactosemia and study of its biochemical characteristics].
    Solov'eva NA; Morozkova TS; Salganik RI
    Genetika; 1975; 11(5):63-71. PubMed ID: 1240812
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. [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]  

  • 5. [Mechanism of enzymatic imprinting induced in rats by an early postnatal administration of galactose].
    Salganik RI; Solov'eva NA; Knorre VL; Tomsons VP; Iurkina EA
    Vopr Med Khim; 1985; 31(4):65-70. PubMed ID: 4049789
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Use of neonatal induction of enzymes for the correction of experimental hereditary enzymopathies].
    Salganik RI; Solov'eva NA; Manankova NM; Tomsons VP
    Vopr Med Khim; 1982; 28(3):8-15. PubMed ID: 6179300
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. Galactose metabolism in mice with galactose-1-phosphate uridyltransferase deficiency: sucklings and 7-week-old animals fed a high-galactose diet.
    Ning C; Reynolds R; Chen J; Yager C; Berry GT; Leslie N; Segal S
    Mol Genet Metab; 2001 Apr; 72(4):306-15. PubMed ID: 11286504
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Metabolic fate of administered [13C]galactose in tissues of galactose-1-phosphate uridyl transferase deficient mice determined by nuclear magnetic resonance.
    Wehrli S; Reynolds R; Segal S
    Mol Genet Metab; 2007 Jan; 90(1):42-8. PubMed ID: 16935536
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Induction of galactose-1-phosphate uridylyltransferase in rat liver by galactose and experimental galactosemia].
    Salganik RI; Solov'eva NA
    Vopr Med Khim; 1972; 18(5):472-7. PubMed ID: 4117776
    [No Abstract]   [Full Text] [Related]  

  • 11. UDP-galactose pyrophosphorylase in mice with galactose-1-phosphate uridyltransferase deficiency.
    Leslie N; Yager C; Reynolds R; Segal S
    Mol Genet Metab; 2005 May; 85(1):21-7. PubMed ID: 15862277
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Termination of experimental galactosemia in rats, and progression of retinal metabolic abnormalities.
    Kowluru RA; Koppolu P
    Invest Ophthalmol Vis Sci; 2002 Oct; 43(10):3287-91. PubMed ID: 12356836
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Prenatal diagnosis of galactose-1-phosphate uridyltransferase (GALT)-deficient galactosemia.
    Elsas LJ
    Prenat Diagn; 2001 Apr; 21(4):302-3. PubMed ID: 11288121
    [No Abstract]   [Full Text] [Related]  

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

  • 16. Stimulation of DNA synthesis and cell proliferation in the liver of rats fed a choline-devoid diet and their suppression by phenobarbital.
    Abanobi SE; Lombardi B; Shinozuka H
    Cancer Res; 1982 Feb; 42(2):412-5. PubMed ID: 7055794
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evidence of cataplerosis in a patient with neonatal classical galactosemia presenting as citrin deficiency.
    Feillet F; Merten M; Battaglia-Hsu SF; Rabier D; Kobayashi K; Straczek J; Brivet M; Favre E; Guéant JL
    J Hepatol; 2008 Mar; 48(3):517-22. PubMed ID: 18207281
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [From gene to disease; galactosemia and galactose-1-phosphate uridyltransferase deficiency].
    Bosch AM; Waterham HR; Bakker HD
    Ned Tijdschr Geneeskd; 2004 Jan; 148(2):80-1. PubMed ID: 14753129
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Expression of galactose-1-phosphate uridyltransferase in the anterior pituitary of rat during the estrous cycle.
    Daude N; Lestage J; Reichardt JK; Petry KG
    Neuroendocrinology; 1996 Jul; 64(1):42-8. PubMed ID: 8811665
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Oxaloacetate induces DNA synthesis and mitosis in primary cultured rat hepatocytes in the absence of EGF.
    Li Y; Sattler GL; Pitot HC
    Biochem Biophys Res Commun; 1993 Jun; 193(3):1339-46. PubMed ID: 8323554
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.