Contribution of UGT1A1 variations to chemotherapy-induced unconjugated hyperbilirubinemia in pediatric leukemia patients

被引:0
作者
Akitaka Nomura
Yoshihiro Maruo
Takashi Taga
Yoshihiro Takeuchi
机构
[1] Shiga University of Medical Science,Department of Pediatrics
来源
Pediatric Research | 2016年 / 80卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:252 / 257
页数:5
相关论文
共 50 条
  • [41] 816 Ugt1A1 Gene Variants in Neonatal Hyperbilirubinemia
    A Kumar
    P K Tiwari
    A Bhutada
    R Agarwal
    R Raman
    Pediatric Research, 2010, 68 : 410 - 410
  • [42] UGT1A1 promoter polymorphism increases risk of nilotinib-induced hyperbilirubinemia
    J B Singer
    Y Shou
    F Giles
    H M Kantarjian
    Y Hsu
    A S Robeva
    P Rae
    A Weitzman
    J M Meyer
    M Dugan
    O G Ottmann
    Leukemia, 2007, 21 : 2311 - 2315
  • [43] Association between hepatic iron deposition, and serum bilirulin levels, mutations of UGT1A1 and HFE gene in patients with hereditary unconjugated hyperbilirubinemia
    Sun, Lei
    Wang, Peng
    Zhang, Liang
    Teng, Xiaoying
    Zhou, Xingang
    Liu, Honggang
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2016, 9 (03): : 3313 - +
  • [44] Analysis of the UGT1A1 Genotype in Hyperbilirubinemia Patients: Differences in Allele Frequency and Distribution
    Mi, Xiao-xiao
    Yan, Jian
    Ma, Xiao-jie
    Zhu, Ge-li
    Gao, Yi-dan
    Yang, Wen-jun
    Kong, Xiao-wen
    Chen, Gong-ying
    Shi, Jun-ping
    Gong, Ling
    BIOMED RESEARCH INTERNATIONAL, 2019, 2019
  • [45] The Effect of UGT1A1 Promoter Polymorphism in the Development of Hyperbilirubinemia and Cholelithiasis in Hemoglobinopathy Patients
    AlFadhli, Suad
    Al-Jafer, Hassan
    Hadi, Mays
    Al-Mutairi, Mashael
    Nizam, Rasheeba
    PLOS ONE, 2013, 8 (10):
  • [46] UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children A retrospective analysis and quantitative correlation
    Abuduxikuer, Kuerbanjiang
    Fang, Ling-Juan
    Li, Li-Ting
    Gong, Jing-Yu
    Wang, Jian-She
    MEDICINE, 2018, 97 (49)
  • [47] UGT1A1 morpholino antisense oligonucleotides produce mild unconjugated hyperbilirubinemia in cyclosporine A-induced cardiovascular disorders in BLC57 mice
    Marghani, Basma H.
    Ateya, Ahmed I.
    Othman, Basma H.
    Rizk, Mohamed Abdo
    El-Adl, Mohamed
    ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2023, 104
  • [48] UGT1A1 polymorphism and hyperbilirubinemia in a patient who received sorafenib
    Meza-Junco, Judith
    Chu, Quincy S. -C.
    Christensen, Olaf
    Rajagopalan, Prabhu
    Das, Soma
    Stefanyschyn, Ruslan
    Sawyer, Michael B.
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2009, 65 (01) : 1 - 4
  • [49] Gilbert or Crigler–Najjar syndrome? Neonatal severe unconjugated hyperbilirubinemia with P364L UGT1A1 homozygosity
    Laura Cozzi
    Federica Nuti
    Irene Degrassi
    Daniela Civeriati
    Giulia Paolella
    Gabriella Nebbia
    Italian Journal of Pediatrics, 48
  • [50] Pazopanib-induced hyperbilirubinemia is associated with Gilbert's syndrome UGT1A1 polymorphism
    Xu, C-F
    Reck, B. H.
    Xue, Z.
    Huang, L.
    Baker, K. L.
    Chen, M.
    Chen, E. P.
    Ellens, H. E.
    Mooser, V. E.
    Cardon, L. R.
    Spraggs, C. F.
    Pandite, L.
    BRITISH JOURNAL OF CANCER, 2010, 102 (09) : 1371 - 1377