Association of KCNJ11 and ABCC8 genetic polymorphisms with response to repaglinide in Chinese diabetic patients

被引：0
|
作者：
Ya-yi He
Rong Zhang
Xin-yu Shao
Cheng Hu
Cong-rong Wang
Jun-xi Lu
Yu-qian Bao
Wei-ping Jia
Kun-san Xiang
机构：
[1] the Sixth People's Hospital,Department of Endocrinology and Metabolism
[2] Shanghai Jiaotong University,undefined
来源：
Acta Pharmacologica Sinica | 2008年 / 29卷
关键词：
repaglinide; polymorphism; pharmacogenomics; type 2 diabetes;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：983 / 989
页数：6
相关论文
共 50 条
  • [21] Could a combination of heterozygous ABCC8 and KCNJ11 mutations cause congenital hyperinsulinism?
    Rozenkova, Klara
    Nessa, Azizun
    Obermannova, Barbora
    Elblova, Lenka
    Dusatkova, Petra
    Sumnik, Zdenek
    Lebl, Jan
    Hussain, Khalid
    Pruhova, Stepanka
    JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2017, 30 (12): : 1311 - 1315
  • [22] Hyperinsulinaemic hypoglycaemia and diabetes mellitus due to dominant ABCC8/KCNJ11 mutations
    R. R. Kapoor
    S. E. Flanagan
    C. T. James
    J. McKiernan
    A. M. Thomas
    S. C. Harmer
    J. P. Shield
    A. Tinker
    S. Ellard
    K. Hussain
    Diabetologia, 2011, 54 : 2575 - 2583
  • [23] The prevalence estimation of PNDM in Poland: the relative contribution of mutations in KCNJ11 and ABCC8 genes
    Klupa, T.
    Gach, A.
    Patch, A.-M.
    Skupien, J.
    Pietrzak, I.
    Ellard, S.
    Hattersley, A.
    Mlynarski, W.
    Malecki, M. T.
    Sieradzki, J.
    DIABETOLOGIA, 2007, 50 : S124 - S124
  • [24] Lack of association between KCNJ11 (rs5219) and ABCC8 (rs757110) polymorphisms and sulphonylurea treatment response in type 2 diabetes patients in Novosibirsk region
    Bondar', I. A.
    Filipenko, M. L.
    Shabel'nikova, O. Yu.
    Sokolova, E. A.
    DIABETES MELLITUS, 2015, 18 (01): : 42 - 47
  • [25] Hyperinsulinism of infancy:: Novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity
    Tornovsky, S
    Crane, A
    Cosgrove, KE
    Hussain, K
    Lavie, J
    Heyman, M
    Nesher, Y
    Kuchinski, N
    Ben-Shushan, E
    Shatz, O
    Nahari, E
    Potikha, T
    Zangen, D
    Tenenbaum-Rakover, Y
    De Vries, L
    Argente, J
    Gracia, R
    Landau, H
    Eliakim, A
    Lindley, K
    Dunne, MJ
    Aguilar-Bryan, L
    Glaser, B
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (12): : 6224 - 6234
  • [26] Screening for Mutations in ABCC8 and KCNJ11 Genes in Saudi Persistent Hyperinsulinemic Hypoglycemia of Infancy (PHHI) Patients
    Adi, Ahmad
    Bin Abbas, Bassam
    Al Hamed, Mohamed
    Al Tassan, Nada
    Bakheet, Dana
    GENES, 2015, 6 (02): : 206 - 215
  • [27] HETEROGENEOUS ISLET CELL ARCHITECTURE OF FOCAL CONGENITAL HYPERINSULINISM DUE TO ABCC8/KCNJ11 MUTATIONS
    Salomon-Estebanez, Maria
    Craigie, Ross J.
    Mal, Walaa
    Han, Bing
    Mosinska, Karolina
    Newbould, Melanie
    Cheesman, Edmund
    Stevens, Adam
    Cosgrove, Karen E.
    Banerjee, Indraneel
    Dunne, Mark J.
    HORMONE RESEARCH IN PAEDIATRICS, 2017, 88 : 468 - 468
  • [28] Effect of genetic variants in KCNJ11, ABCC8, PPARG and HNF4A loci on the susceptibility of type 2 diabetes in Chinese Han population
    Wang Fang
    Han Xue-yao
    Ren Qian
    Zhang Xiu-ying
    Han Ling-chuan
    Luo Ying-ying
    Zhou Xiang-hai
    Ji Li-nong
    CHINESE MEDICAL JOURNAL, 2009, 122 (20) : 2477 - 2482
  • [29] Integration of genomic analysis and transcript expression of ABCC8 and KCNJ11 in focal form of congenital hyperinsulinism
    Wieland, Ilse
    Schanze, Ina
    Felgendreher, Ina Marianti
    Barthlen, Winfried
    Vogelgesang, Silke
    Mohnike, Klaus
    Zenker, Martin
    FRONTIERS IN ENDOCRINOLOGY, 2022, 13
  • [30] Mutational analysis of ABCC8, KCNJ11, GLUD1, HNF4A and GCK genes in 30 Chinese patients with congenital hyperinsulinism
    Sang, Yanmei
    Xu, Zidi
    Liu, Min
    Yan, Jie
    Wu, Yujun
    Zhu, Cheng
    Ni, Guichen
    ENDOCRINE JOURNAL, 2014, 61 (09) : 901 - 910
12345