ウリジルトランスフェラーゼ
- 関
- UDPglucose-hexose-1-phosphate uridylyltransferase
WordNet
- any of various enzymes that move a chemical group from one compound to another compound
UpToDate Contents
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English Journal
- Electrophilic and reactive oxygen species detoxification potentials of chalcone dimers is mediated by redox transcription factor Nrf-2.
- Ajiboye TO1, Yakubu MT, Oladiji AT.
- Journal of biochemical and molecular toxicology.J Biochem Mol Toxicol.2014 Jan;28(1):11-22. doi: 10.1002/jbt.21517. Epub 2013 Aug 20.
- Nuclear erythroid related factor-2 (Nrf2), a redox-transcription factor, plays a critical role in the detoxification of electrophilic and reactive oxygen species that halt various biochemical and molecular processes. This makes it a candidate for regulation by polyphenols. This study investigates th
- PMID 23963778
- Unraveling the Leloir pathway of Bifidobacterium bifidum: significance of the uridylyltransferases.
- De Bruyn F1, Beauprez J, Maertens J, Soetaert W, De Mey M.
- Applied and environmental microbiology.Appl Environ Microbiol.2013 Nov;79(22):7028-35. doi: 10.1128/AEM.02460-13. Epub 2013 Sep 6.
- The GNB/LNB (galacto-N-biose/lacto-N-biose) pathway plays a crucial role in bifidobacteria during growth on human milk or mucin from epithelial cells. It is thought to be the major route for galactose utilization in Bifidobacterium longum as it is an energy-saving variant of the Leloir pathway. Both
- PMID 24014529
- Galactosemia in the Turkish population with a high frequency of Q188R mutation and distribution of Duarte-1 and Duarte-2 variations.
- Özgül RK1, Güzel-Ozantürk A, Dündar H, Yücel-Yılmaz D, Coşkun T, Sivri S, Aydoǧdu S, Tokatlı A, Dursun A.
- Journal of human genetics.J Hum Genet.2013 Oct;58(10):675-8. doi: 10.1038/jhg.2013.76. Epub 2013 Aug 8.
- Classical galactosemia is an inherited recessive disorder of galactose metabolism caused by deficiency of the enzyme galactose-1-phosphate uridyl transferase (GALT), which is caused by mutations in the GALT gene. In this study, 56 Turkish patients diagnosed with galactosemia were screened for GALT g
- PMID 23924834
Japanese Journal
- Endometriosis associated with the N314D mutation of galactose-1-phosphate uridyl transferase (GALT)
- Vaginal agenesis (Mayer-Rokitansky-Kuster-Hauser syndrome) associated with the N314D mutation of galactose-1-phosphate uridyl transferase (GALT)
Related Links
- Clinical Use: Clinicians use galactose-1-phosphate uridyl transferase to diagnose Galactose-1-phosphate uridyl transferase deficiency which is the most common cause of galactosemia and can be used a confirmation for abnormal ...
- Revised: 01/21/94 Page 2 of 4 Enzymatic Assay of GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE (EC 2.7.7.12) REAGENTS: (continued) D. 0.2 mM Glucose 1,6-Diphosphate Solution (G 1,6-DiP) (Prepare 1 ml in ...
★リンクテーブル★
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- 英
- uridyl transferase
- 関
- UDPグルコース・ヘキソース-1-リン酸ウリジルトランスフェラーゼ
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UDPグルコース・ヘキソース-1-リン酸ウリジルトランスフェラーゼ
- 関
- uridyl transferase
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ガラクトース-1-リン酸ウリジルトランスフェラーゼ GALT
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ガラクトース-1-リン酸ウリジルトランスフェラーゼ
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- 関
- lyase、synthase、transposase
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トランスフェラーゼ