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 *

153 related articles for article (PubMed ID: 27796522)

  • 1. The association between MEFV gene polymorphisms and Henoch-Schönlein purpura, and additional SNP-SNP interactions in Chinese Han children.
    Xiong S; Xiong Y; Huang Q; Wang J; Zhang X
    Rheumatol Int; 2017 Mar; 37(3):455-460. PubMed ID: 27796522
    [TBL] [Abstract][Full Text] [Related]  

  • 2. MEFV E148Q polymorphism is associated with Henoch-Schönlein purpura in Chinese children.
    He X; Lu H; Kang S; Luan J; Liu Z; Yin W; Yao H; Ding Y; Li T; Heng CK
    Pediatr Nephrol; 2010 Oct; 25(10):2077-82. PubMed ID: 20602240
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association between IL17A and IL17F polymorphisms and risk of Henoch-Schonlein purpura in Chinese children.
    Xu H; Pan Y; Li W; Fu H; Zhang J; Shen H; Han X
    Rheumatol Int; 2016 Jun; 36(6):829-35. PubMed ID: 27021337
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inducible nitric oxide synthase gene polymorphisms are associated with a risk of nephritis in Henoch-Schönlein purpura children.
    Jiang J; Duan W; Shang X; Wang H; Gao Y; Tian P; Zhou Q
    Eur J Pediatr; 2017 Aug; 176(8):1035-1045. PubMed ID: 28593405
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A study on the association between C1GALT1 polymorphisms and the risk of Henoch-Schönlein purpura in a Chinese population.
    An J; Lü Q; Zhao H; Cao Y; Yan B; Ma Z
    Rheumatol Int; 2013 Oct; 33(10):2539-42. PubMed ID: 23624553
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Heat shock protein 70-2 and tumor necrosis factor-α gene polymorphisms in Chinese children with Henoch-Schönlein purpura.
    Ding GX; Wang CH; Che RC; Guan WZ; Yuan YG; Su M; Zhang AH; Huang SM
    World J Pediatr; 2016 Feb; 12(1):49-54. PubMed ID: 26547206
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of adiponectin gene polymorphisms and additional gene-gene interaction with nonalcoholic fatty liver disease in the Chinese Han population.
    Wei Z; Li-Qun Z; Xiao-Ling H; Jian Q; Guo-Yue Y
    Hepatol Int; 2016 May; 10(3):511-7. PubMed ID: 26865047
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Impact of the PDE4D gene polymorphism and additional SNP-SNP and gene-smoking interaction on ischemic stroke risk in Chinese Han population.
    Wang X; Sun Z; Zhang Y; Tian X; Li Q; Luo J
    Neurol Res; 2017 Apr; 39(4):351-356. PubMed ID: 28191858
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Association of CYP1A1 Gene With Cervical Cancer and Additional SNP-SNP Interaction in Chinese Women.
    Li S; Li G; Kong F; Liu Z; Li N; Li Y; Guo X
    J Clin Lab Anal; 2016 Nov; 30(6):1220-1225. PubMed ID: 27265845
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Interaction between SELP genetic polymorphisms with inflammatory cytokine interleukin-6 (IL-6) gene variants on cardiovascular disease in Chinese Han population.
    Kou L; Yang N; Dong B; Li Y; Yang J; Qin Q
    Mamm Genome; 2017 Oct; 28(9-10):436-442. PubMed ID: 28819827
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Case-Control Study on Impact of the Telomerase Reverse Transcriptase Gene Polymorphism and Additional Single Nucleotide Polymorphism (SNP)- SNP Interaction on Non-Small Cell Lung Cancers Risk in Chinese Han Population.
    Xing YL; Liu F; Li JF; Lin JC; Zhu GD; Li M; Zhang CR; Niu YY
    J Clin Lab Anal; 2016 Nov; 30(6):1071-1077. PubMed ID: 27154632
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Interferon-gamma gene polymorphism +874 (a/t) in Chinese children with Henoch-Schonlein purpura.
    Xu H; Li W; Fu H; Jiang G
    Iran J Allergy Asthma Immunol; 2014 Jun; 13(3):184-9. PubMed ID: 24659122
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The association of CYP1A1 genetic polymorphisms and additional gene-gene interaction with ischemic stroke in the eastern Han of China.
    Zhang M; Wu JM; Zhang QS; Yan DW; Ren LJ; Li WP
    Neurol Sci; 2016 Oct; 37(10):1679-84. PubMed ID: 27383824
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Impact of interaction between the G870A and EFEMP1 gene polymorphism on glioma risk in Chinese Han population.
    Yang L; Qu B; Xia X; Kuang Y; Li J; Fan K; Guo H; Zheng H; Ma Y
    Oncotarget; 2017 Jun; 8(23):37561-37567. PubMed ID: 28380465
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chemokine MCP1/CCL2 and RANTES/CCL5 gene polymorphisms influence Henoch-Schönlein purpura susceptibility and severity.
    Yu HH; Liu PH; Yang YH; Lee JH; Wang LC; Chen WJ; Chiang BL
    J Formos Med Assoc; 2015 Apr; 114(4):347-52. PubMed ID: 25839768
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association of Endothelial Nitric Oxide Synthase Gene Polymorphism with Susceptibility and Nephritis Development of Henoch-Schönlein Purpura in Chinese Han Children.
    Wang A; Wang A; Xiao Y; Wang J; Xu E
    Genet Test Mol Biomarkers; 2017 Jun; 21(6):373-381. PubMed ID: 28409662
    [TBL] [Abstract][Full Text] [Related]  

  • 17. MEFV gene variants in children with Henoch-Schönlein purpura and association with clinical manifestations: a single-center Mediterranean experience.
    Ekinci RMK; Balci S; Bisgin A; Atmis B; Dogruel D; Altintas DU; Yilmaz M
    Postgrad Med; 2019 Jan; 131(1):68-72. PubMed ID: 30513227
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Impact of CRP gene and additional gene-smoking interaction on ischemic stroke in a Chinese Han population.
    Wu Z; Huang Y; Huang J; Fan L
    Neurol Res; 2017 May; 39(5):442-447. PubMed ID: 28287042
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Gene- Gene Interaction between PPARG and APOE Gene on Late-Onset Alzheimer's Disease: A Case- Control Study in Chinese Han Population.
    Wang S; Guan L; Luo D; Liu J; Lin H; Li X; Liu X
    J Nutr Health Aging; 2017; 21(4):397-403. PubMed ID: 28346566
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of ACE, VEGF and CCL2 gene polymorphisms with Henoch-Schönlein purpura and an evaluation of the possible interaction effects of these loci in HSP patients.
    Mohammadian T; Bonyadi M; Nabat E; Rafeey M
    Adv Clin Exp Med; 2017 Jul; 26(4):661-664. PubMed ID: 28691415
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.