WordNet

any of various enzymes that move a chemical group from one compound to another compound

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1. ヘキソースリン酸側路およびグルタチオン代謝疾患（グルコース-6-リン酸脱水素酵素欠損症を除く） disorders of the hexose monophosphate shunt and glutathione metabolism other than glucose 6 phosphate dehydrogenase deficiency
2. 尿路上皮（移行上皮）膀胱癌の疫学および病因 epidemiology and etiology of urothelial transitional cell carcinoma of the bladder
3. 慢性閉塞性肺疾患（COPD）：危険因子およびリスク低減 chronic obstructive pulmonary disease risk factors and risk reduction
4. 前立腺癌の分子生物学 molecular biology of prostate cancer
5. ビリルビン代謝 bilirubin metabolism

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

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)

リンク元	「ウリジルトランスフェラーゼ」「UDPglucose-hexose-1-phosphate uridylyltransferase」
拡張検索	「galactose-1-phosphate uridyl transferase」「galactose 1-phosphate uridyl transferase」
関連記事	「transferase」「transferases」