IMPDH1 AND IMPDH2 PHARMACOGENETICS: GENE SEQUENCE VARIATION AND FUNCTIONAL GENOMICS.

被引：0
|
作者：
Wu, T. [1 ]
Pelleymounter, L. L. [1 ]
Moon, I. [1 ]
Weinshilboum, R. M. [1 ]
机构：
[1] Mayo Clin, Rochester, MN USA
来源：
CLINICAL PHARMACOLOGY & THERAPEUTICS | 2010年 / 87卷
关键词：
D O I：
暂无
中图分类号：
R9 [药学];
学科分类号：
1007 ;
摘要：
引用
收藏
页码：S5 / S5
页数：1
相关论文
共 50 条
  • [31] Lymphocyte Counts in Kidney Allograft Recipients Are Associated With IMPDH2 3757T>C Gene Polymorphism
    Pazik, J.
    Oldak, M.
    Podgorska, M.
    Lewandowski, Z.
    Sitarek, E.
    Ploski, R.
    Szmidt, J.
    Chmura, A.
    Durlik, M.
    Malejczyk, J.
    TRANSPLANTATION PROCEEDINGS, 2011, 43 (08) : 2943 - 2945
  • [32] Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa
    Bowne, SJ
    Sullivan, LS
    Blanton, SH
    Cepko, CL
    Blackshaw, S
    Birch, DG
    Hughbanks-Wheaton, D
    Heckenlively, JR
    Daiger, SP
    HUMAN MOLECULAR GENETICS, 2002, 11 (05) : 559 - 568
  • [33] ZNRD1 mediates resistance of gastric cancer cells to methotrexate by regulation of IMPDH2 and Bcl-2
    Hong, Liu
    Qiao, Taidong
    Han, Yu
    Han, Shuang
    Zhang, Xiaoyin
    Lin, Tao
    Gao, Juan
    Zhao, Pengtao
    Chen, Zhen
    Fan, Daiming
    BIOCHEMISTRY AND CELL BIOLOGY, 2006, 84 (02) : 199 - 206
  • [34] Mycophenolate Mofetil Selection of Gene Modified T Cells With an Engineered Human Inosine Monophosphate Dehydrogenase II (IMPDH2)
    Jonnalagadda, Mahesh
    Chang, Wen-Chung
    Jensen, Michael C.
    JOURNAL OF IMMUNOTHERAPY, 2008, 31 (09) : 923 - 923
  • [35] Identification of IMPDH1 as the gene for RP10 following microarray analysis: Implications for detection of other retinal disease genes
    Kennan, A
    Aherne, A
    Palfi, A
    Humphries, M
    Demtroder, K
    Orntoft, T
    Ayuso, C
    Farrar, J
    Kenna, PF
    Humphries, P
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2002, 43 : U179 - U179
  • [36] Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa
    Bowne, SJ
    Sullivan, LS
    Blanton, SH
    Cepko, CL
    Blackshaw, S
    Birch, DG
    Hughbanks-Wheaton, D
    Heckenlively, JR
    Daiger, SP
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2002, 43 : U179 - U179
  • [37] MYBL2 regulates de novo purine synthesis by transcriptionally activating IMPDH1 in hepatocellular carcinoma cells
    Zhao, Jun-Zhang
    Wang, Wei
    Liu, Tao
    Zhang, Lei
    Lin, De-Zheng
    Yao, Jia-Yin
    Peng, Xiang
    Jin, Gang
    Ma, Tian-Tian
    Gao, Jin-Bo
    Huang, Fang
    Nie, Jun
    Lv, Qing
    BMC CANCER, 2022, 22 (01)
  • [38] SHIV KU-1感染恒河猴颞叶皮层中IMPDH2的表达
    赵长城
    丁华明
    鹿伦山
    张千
    杨静
    董颖
    薛群山
    庄柯
    中国比较医学杂志, 2023, (07) : 34 - 40
  • [39] Pharmacogenetics of human 3′-phosphoadenosine 5′-phosphosulfate synthetase 1 (PAPSS1):: gene resequencing, sequence variation, and functional genomics
    Xu, ZH
    Thomae, BA
    Eckloff, BW
    Wieben, ED
    Weinshilboum, RM
    BIOCHEMICAL PHARMACOLOGY, 2003, 65 (11) : 1787 - 1796
  • [40] MYBL2 regulates de novo purine synthesis by transcriptionally activating IMPDH1 in hepatocellular carcinoma cells
    Jun-Zhang Zhao
    Wei Wang
    Tao Liu
    Lei Zhang
    De-Zheng Lin
    Jia-Yin Yao
    Xiang Peng
    Gang Jin
    Tian-Tian Ma
    Jin-Bo Gao
    Fang Huang
    Jun Nie
    Qing Lv
    BMC Cancer, 22
12345