期刊文献+

新生儿高未结合胆红素血症代谢通路相关的遗传学研究进展 被引量:6

原文传递
导出
摘要 新生儿高胆红素血症是胆红素的产生与代谢能力不平衡所致,其病因复杂,遗传因素对胆红素的影响越来越被人们所认识。胆红素代谢途径的相关研究中,尿苷二磷酸葡萄糖醛酸转移酶(uridine diphosphate glucuronosyltransferase,UGT)、有机阴离子转运多肽(organic anion transporting polypeptide,OATP)、血红素加氧酶(heme oxygenase,HO)、胆绿素还原酶(biliverdin reductase,BLVRA)4个基因与新生儿高胆红素血症的相关性报道较多。本文对以上4个基因的研究进展进行综述。
出处 《中华新生儿科杂志(中英文)》 CAS 2019年第2期144-146,共3页 Chinese Journal of Neonatology
  • 相关文献

参考文献3

二级参考文献150

  • 1Shabana Farheen,Sanghamitra Sengupta,Amal Santra,Suparna Pal,Gopal Krishna Dhali,Meenakshi Chakravorty,Partha P Majumder,Abhijit Chowdhury.Gilbert's syndrome: High frequency of the (TA)_7 TAA allele in India and its interaction with a novel CAT insertion in promoter of the gene for bilirubin UDP-glucuronosyltransferase 1 gene[J].World Journal of Gastroenterology,2006,12(14):2269-2275. 被引量:29
  • 2Dilek Iusuf,Evita van de Steeg,Alfred H. Schinkel.Functions of OATP1A and 1B transporters in vivo: insights from mouse models[J]. Trends in Pharmacological Sciences . 2011 (2)
  • 3MeganRoth,AmandaObaidat,BrunoHagenbuch.OATPs, OATs and OCTs: the organic anion and cation transporters of the SLCO and SLC22A gene superfamilies[J]. British Journal of Pharmacology . 2012 (5)
  • 4van de Steeg, Evita,Stránecky, Viktor,Hartmannová, Hana,Nosková, Lenka,Hrebícek, Martin,Wagenaar, Els,van Esch, Anita,de Waart, Dirk R,Elferink, Ronald P J Oude,Kenworthy, Kathryn E,Sticová, Eva,al-Edreesi, Mohammad,Knisely, A S,Kmoch, Stanislav,Jirsa, Milan,Schinkel, Alfred H.Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liver[J]. EN . 2012 (2)
  • 5van de Steeg, Evita,Wagenaar, Els,van der Kruijssen, Cornelia M M,Burggraaff, Johanna E C,de Waart, Dirk R,Elferink, Ronald P J Oude,Kenworthy, Kathryn E,Schinkel, Alfred H.Organic anion transporting polypeptide 1a/1b-knockout mice provide insights into hepatic handling of bilirubin, bile acids, and drugs[J]. Journal of Clinical Investigation . 2010 (8)
  • 6MartinLacko,Hennie M.J.Roelofs,Rene H.M.te Morsche,Adri C.Voogd,Michel B. OudeOphuis,Wilbert H.M.Peters,Johannes J.Manni.Genetic polymorphism in the conjugating enzyme UGT1A1 and the risk of head and neck cancer[J]. Int. J. Cancer . 2010 (12)
  • 7Tristan M. Sissung,Caitlin E. Baum,C. Tyler Kirkland,Rui Gao,Erin R. Gardner,William D. Figg.Pharmacogenetics of Membrane Transporters: An Update on Current Approaches[J]. Molecular Biotechnology . 2010 (2)
  • 8AnnikkaKalliokoski,MikkoNeuvonen,Pertti J.Neuvonen,MikkoNiemi.The effect of SLCO1B1 polymorphism on repaglinide pharmacokinetics persists over a wide dose range[J]. British Journal of Clinical Pharmacology . 2008 (6)
  • 9Wandee Udomuksorn,David J. Elliot,Benjamin C. Lewis,Peter I. Mackenzie,Krongtong Yoovathaworn,John O. Miners.Influence of mutations associated with Gilbert and Crigler–Najjar type II syndromes on the glucuronidation kinetics of bilirubin and other UDP-glucuronosyltransferase 1A substrates[J]. Pharmacogenetics and Genomics . 2007 (12)
  • 10Waddah A. Alrefai,Ravinder K. Gill.Bile Acid Transporters: Structure, Function, Regulation and Pathophysiological Implications[J]. Pharmaceutical Research . 2007 (10)

共引文献47

同被引文献47

引证文献6

二级引证文献19

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部