نتایج جستجو برای: slco1b1

تعداد نتایج: 546  

2016
Yi-Hao Weng Ya-Wen Chiu Shao-Wen Cheng Chun-Yuh Yang

BACKGROUND Hyperbilirubinemia is a common disorder during neonatal period in Taiwan. Gene variants may play an important role in the development of neonatal hyperbilirubinemia. The current study investigated the association between neonatal hyperbilirubinemia and common gene variants involving the production and metabolism of bilirubin. METHODS This prospective study enrolled 444 healthy infa...

2015
Hui Yang Qian Wang Lei Zheng Min Lin Xiang-bin Zheng Fen Lin Li-Ye Yang Tonse Raju

The potential for genetic variation to modulate neonatal hyperbilirubinemia risk is increasingly being recognized. A case-control study was designed to assess comprehensive contributions of the multiple genetic modifiers of bilirubin metabolism on significant neonatal hyperbilirubinemia in Chinese descendents. Eleven common mutations and polymorphisms across five bilirubin metabolism genes, nam...

2017
S Bins L van Doorn MA Phelps AA Gibson S Hu L Li A Vasilyeva G Du P Hamberg FALM Eskens P de Bruijn A Sparreboom RHJ Mathijssen SD Baker

The oral multikinase inhibitor sorafenib undergoes extensive UGT1A9-mediated formation of sorafenib-β-D-glucuronide (SG). Using transporter-deficient mouse models, it was previously established that SG can be extruded into bile by ABCC2 or follow a liver-to-blood shuttling loop via ABCC3-mediated efflux into the systemic circulation, and subsequent uptake in neighboring hepatocytes by OATP1B-ty...

2014
Mojca Zajc Avramovič Nataša Toplak Meta Accetto Maruša Debeljak Lara Lusa Vita Dolžan Tadej Avčin

Methods The data of 116 consecutive patients with JIA treated with MTX at the University Children’s Hospital Ljubljana from June 2011 to May 2014 have been retrospectively reviewed. The disease activity was measured by JADAS 71 score 3 and 6 months after the beginning of treatment with MTX and at the last follow up visit. All adverse events were noted separately for different organ systems. Gen...

Journal: :Journal of the American College of Cardiology 2009

Journal: :European Heart Journal 2022

Abstract Background Statins are a cornerstone therapy for management of hypercholesterolaemia in primary and secondary prevention cardiovascular disease, however there is individual variation regarding efficacy adverse side-effects experienced. Purpose Polymorphisms the SLCO1B1 gene have shown correlation with risk statin treatment, real-world clinical practice, their utility remains to be esta...

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