These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 22093981)

  • 1. [Association of single nucleotide polymorphism in human CYP8B1 gene with gallstone disease].
    Qin J; Jiang ZY; Niu ZM; Zhang KY; Hua Q; Jiang ZH; Wang Y; Huang W; Han TQ; Zhang SD
    Zhonghua Yi Xue Za Zhi; 2011 Aug; 91(30):2092-5. PubMed ID: 22093981
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Single nucleotide polymorphism rs3732860 in the 3'-untranslated region of CYP8B1 gene is associated with gallstone disease in Han Chinese.
    Qin J; Han TQ; Yuan WT; Zhang J; Fei J; Jiang ZY; Niu ZM; Zhang KY; Hua Q; Cai XX; Xu SJ; Huang W; Zhang SD
    J Gastroenterol Hepatol; 2013 Apr; 28(4):717-22. PubMed ID: 23216301
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of three common single nucleotide polymorphisms of ATP binding cassette G8 gene with gallstone disease: a meta-analysis.
    Jiang ZY; Cai Q; Chen EZ
    PLoS One; 2014; 9(1):e87200. PubMed ID: 24498041
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fibroblast growth factor receptor 4 Gly388Arg polymorphism associated with severity of gallstone disease in a Chinese population.
    Chen Q; Li WJ; Wan YY; Yu CD; Li WG
    Genet Mol Res; 2012 Mar; 11(1):548-55. PubMed ID: 22535390
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Reabsorption of bile acids regulated by FXR-OATP1A2 is the main factor for the formation of cholesterol gallstone.
    Cai J; Wang Z; Chen G; Li D; Liu J; Hu H; Qin J
    Am J Physiol Gastrointest Liver Physiol; 2020 Sep; 319(3):G303-G308. PubMed ID: 32597704
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [No association between 3 polymorphisms of transforming growth factor beta3 gene and essential hypertension in Chinese].
    Hu BC; Chu SL; Wang JG; Wang GL; Gao PJ; Zhu DL
    Zhonghua Xin Xue Guan Bing Za Zhi; 2005 Feb; 33(2):127-31. PubMed ID: 15924806
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of -394C>G and -420C>G polymorphisms in the RETN gene with T2DM and CHD and a new potential SNP might be exist in exon 3 of RETN gene in Chinese.
    Chi S; Lan C; Zhang S; Liu H; Wang X; Chen Y; Chen X; Chen S; Zhang W
    Mol Cell Biochem; 2009 Oct; 330(1-2):31-8. PubMed ID: 19381781
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Association of single nucleotide polymorphism in human SCN7A gene with essential hypertension in Chinese].
    Zhang KX; Zhu DL; He X; Zhang Y; Zhang H; Zhao R; Lin J; Wang GL; Zhang KY; Huang W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Dec; 20(6):463-7. PubMed ID: 14669210
    [TBL] [Abstract][Full Text] [Related]  

  • 9. ATP binding cassette G8 T400K polymorphism may affect the risk of gallstone disease among Chinese males.
    Wang Y; Jiang ZY; Fei J; Xin L; Cai Q; Jiang ZH; Zhu ZG; Han TQ; Zhang SD
    Clin Chim Acta; 2007 Sep; 384(1-2):80-5. PubMed ID: 17612515
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cholesterol 7alpha-hydrolase (CYP7A1) c.-278A>C promoter polymorphism in gallstone disease patients.
    Juzyszyn Z; Kurzawski M; Lener A; Modrzejewski A; Pawlik A; Droździk M
    Genet Test; 2008 Mar; 12(1):97-100. PubMed ID: 18307386
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Study on single nucleotide polymorphism of TLR4 in Chinese population].
    Feng K; Zhou GQ; Zhai Y; Zhu PF; Wang ZG; He FC; Jiang JX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):99-101. PubMed ID: 15696495
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Mitochondrial DNA Variant Elevates the Risk of Gallstone Disease by Altering Mitochondrial Function.
    Sun D; Niu Z; Zheng HX; Wu F; Jiang L; Han TQ; Wei Y; Wang J; Jin L
    Cell Mol Gastroenterol Hepatol; 2021; 11(4):1211-1226.e15. PubMed ID: 33279689
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic effect of single-nucleotide polymorphisms in the PPARGC1B gene on airway hyperreactivity in asthmatic patients.
    Lee SH; Jang AS; Woo Park S; Park JS; Kim YK; Uh ST; Kim YH; Chung IY; Park BL; Shin HD; Park CS
    Clin Exp Allergy; 2011 Nov; 41(11):1533-44. PubMed ID: 21692888
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of RAC1 Gene Polymorphisms with Primary End-Stage Renal Disease in Chinese Renal Recipients.
    Liu Y; Zhou J; Luo X; Yang C; Zhang Y; Shi S
    PLoS One; 2016; 11(2):e0148270. PubMed ID: 26841219
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association between PLA2G12A Polymorphisms and Schizophrenia in a Han Chinese Population from Northeast China.
    Yang G; Xu H; Zhang H; Yu Q; Wu Y; Shi J; Rao W; You Y; Kou C; Yu Y
    PLoS One; 2016; 11(7):e0159584. PubMed ID: 27434078
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CT60 single nucleotide polymorphism of the CTLA-4 gene is associated with susceptibility to Graves' disease in the Taiwanese population.
    Weng YC; Wu MJ; Lin WS
    Ann Clin Lab Sci; 2005; 35(3):259-64. PubMed ID: 16081581
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Association of the exon 8 and intron 8 polymorphisms of the human urate transporter 1 gene with primary hyperuricemia in Chinese Han population].
    Meng DM; Han L; Miao ZM; Li CG
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Dec; 27(6):659-63. PubMed ID: 21154327
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A variant of the SLC10A2 gene encoding the apical sodium-dependent bile acid transporter is a risk factor for gallstone disease.
    Renner O; Harsch S; Schaeffeler E; Winter S; Schwab M; Krawczyk M; Rosendahl J; Wittenburg H; Lammert F; Stange EF
    PLoS One; 2009 Oct; 4(10):e7321. PubMed ID: 19823678
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Missense polymorphisms within IL-10R1 exons are not associated with systemic lupus erythematosus in Chinese.
    Cui H; Xue H; Yang L; Liu D; Qi L; Zhang N
    Lupus; 2012 Oct; 21(11):1232-6. PubMed ID: 22652629
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The Potential Mutation of GAK Gene in the Typical Sporadic Parkinson's Disease from the Han Population of Chinese Mainland.
    Zhang J; Zeng H; Zhu L; Deng L; Fang X; Deng X; Liang H; Tang C; Cao X; Lu Y; Li J; Ren X; Zuo W; Zhang X; Xu R
    Mol Neurobiol; 2016 Dec; 53(10):7119-7136. PubMed ID: 26676575
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.