82 related articles for article (PubMed ID: 4049789)
1. [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]
2. [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]
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. [Enzymatic "imprinting" as a result of exposure to genetic enzyme inducers soon after the birth of animals].
Salganik RI; Griaznova IM; Markel' AL; Manankova NM; Solov'eva NA
Dokl Akad Nauk SSSR; 1979; 245(2):473-6. PubMed ID: 35317
[No Abstract] [Full Text] [Related]
5. [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]
6. [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]
7. [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]
8. [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]
9. Modulation of rat tissue galactose-1-phosphate uridyltransferase by uridine and uridine triphosphate.
Rogers S; Segal S
Pediatr Res; 1991 Sep; 30(3):222-6. PubMed ID: 1945559
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. Galactosemia caused by a point mutation that activates cryptic donor splice site in the galactose-1-phosphate uridyltransferase gene.
Wadelius C; Lagerkvist A; Molin AK; Larsson A; von Döbeln U; Pettersson U
Genomics; 1993 Aug; 17(2):525-6. PubMed ID: 8406510
[No Abstract] [Full Text] [Related]
12. [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]
13. 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]
14. Pathways of galactose metabolism by galactosemics: evidence for galactose conversion to hepatic UDPglucose.
Segal S; Wehrli S; Yager C; Reynolds R
Mol Genet Metab; 2006 Feb; 87(2):92-101. PubMed ID: 16260165
[TBL] [Abstract][Full Text] [Related]
15. [Changes in the RNA-dependent DNA-polymerase activity of retrovirus-like particles in the rat liver during postnatal ontogeny].
Pyrinova GB; Korokhov NP; Kiseleva EV; Tomsons VP; Khristoliubova NB
Ontogenez; 1984; 15(6):637-43. PubMed ID: 6084211
[TBL] [Abstract][Full Text] [Related]
16. Evidence for alternate galactose oxidation in a patient with deletion of the galactose-1-phosphate uridyltransferase gene.
Berry GT; Leslie N; Reynolds R; Yager CT; Segal S
Mol Genet Metab; 2001 Apr; 72(4):316-21. PubMed ID: 11286505
[TBL] [Abstract][Full Text] [Related]
17. Duarte allele impairs biostability of galactose-1-phosphate uridyltransferase in human lymphoblasts.
Lai K; Langley SD; Dembure PP; Hjelm LN; Elsas LJ
Hum Mutat; 1998; 11(1):28-38. PubMed ID: 9450900
[TBL] [Abstract][Full Text] [Related]
18. [Stable changes in the nuclear matrix activity and DNA structure of the liver in rats due to neonatal induction of gene expression].
Salganik RI; Knorre VL; Drevich VF; Morozova OV; Zaĭchikov EF
Dokl Akad Nauk SSSR; 1985; 281(5):1237-41. PubMed ID: 2408837
[No Abstract] [Full Text] [Related]
19. 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]
20. Functional analysis of the human galactose-1-phosphate uridyltransferase promoter in Duarte and LA variant galactosemia.
Elsas LJ; Lai K; Saunders CJ; Langley SD
Mol Genet Metab; 2001 Apr; 72(4):297-305. PubMed ID: 11286503
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
