137 related articles for article (PubMed ID: 28963667)
1. The association between genetic variation in interleukin-10 gene and susceptibility to Henoch-Schönlein purpura in Chinese children.
Xu H; Jiang G; Shen H; Pan Y; Zhang J; Li W; Mao J
Clin Rheumatol; 2017 Dec; 36(12):2761-2767. PubMed ID: 28963667
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Association of TLR4 gene polymorphisms with childhood Henoch-Schönlein purpura in a Chinese population.
Xu H; Jiang G; Shen H; Li W; Mao J; Pan Y
Rheumatol Int; 2017 Nov; 37(11):1909-1915. PubMed ID: 28905155
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Lack of association between macrophage migration inhibitory factor gene promoter (-173 G/C) polymorphism and childhood Henoch-Schönlein purpura in Turkish patients.
Nalbantoglu S; Tabel Y; Mir S; Berdeli A
Cytokine; 2013 Apr; 62(1):160-4. PubMed ID: 23523092
[TBL] [Abstract][Full Text] [Related]
7. Association between HLA-A and -B polymorphisms and susceptibility to Henoch-Schönlein purpura in Han and Mongolian children from Inner Mongolia.
Ren SM; Yang GL; Liu CZ; Zhang CX; Shou QH; Yu SF; Li WC; Su XL
Genet Mol Res; 2012 Feb; 11(1):221-8. PubMed ID: 22370889
[TBL] [Abstract][Full Text] [Related]
8. Association of mannose binding lectin codon 54 polymorphism with predisposition to Henoch-Schönlein purpura in childhood.
Durmaz B; Aykut A; Hursitoglu G; Bak M; Serdaroglu E; Onay H; Ozkinay F
Int J Rheum Dis; 2014 Mar; 17(3):317-20. PubMed ID: 24576294
[TBL] [Abstract][Full Text] [Related]
9. Renin-angiotensin system gene polymorphisms: association with susceptibility to Henoch-Schonlein purpura and renal involvement.
Ozkaya O; Söylemezoğlu O; Gönen S; Misirlioğlu M; Tuncer S; Kalman S; Buyan N; Hasanoğlu E
Clin Rheumatol; 2006 Nov; 25(6):861-5. PubMed ID: 16521052
[TBL] [Abstract][Full Text] [Related]
10. Role of PTPN22 and CSK gene polymorphisms as predictors of susceptibility and clinical heterogeneity in patients with Henoch-Schönlein purpura (IgA vasculitis).
López-Mejías R; Genre F; Remuzgo-Martínez S; Pérez BS; Castañeda S; Llorca J; Ortego-Centeno N; Ubilla B; Mijares V; Pina T; Calvo-Río V; Palmou N; Miranda-Filloy JA; Parejo AN; Argila D; Sánchez-Pérez J; Rubio E; Luque ML; Blanco-Madrigal JM; Galíndez-Aguirregoikoa E; Ocejo-Vinyals JG; Martín J; Blanco R; González-Gay MA
Arthritis Res Ther; 2015 Oct; 17():286. PubMed ID: 26458874
[TBL] [Abstract][Full Text] [Related]
11. No evidence of association between functional polymorphisms located within IL6R and IL6ST genes and Henoch-Schönlein purpura.
López-Mejías R; Sevilla Pérez B; Genre F; Castañeda S; Ortego-Centeno N; Llorca J; Ubilla B; Ochoa R; Pina T; Marquez A; Sala-Icardo L; Miranda-Filloy JA; Rueda-Gotor J; Martín J; Blanco R; González-Gay MA
Tissue Antigens; 2013 Dec; 82(6):416-9. PubMed ID: 24498998
[TBL] [Abstract][Full Text] [Related]
12. Association of the paired box 2 gene polymorphism with the susceptibility and pathogenesis of Henoch‑Schönlein purpura in children.
Chen J; Fang X; Dang X; Wu X; Yi Z
Mol Med Rep; 2015 Mar; 11(3):1997-2003. PubMed ID: 25385517
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Association study between matrix metalloproteinase-9 gene (MMP9) polymorphisms and the risk of Henoch-Schönlein purpura in children.
Xu ED; Xiao YF; Wang JJ; Dong L
Genet Mol Res; 2016 Jun; 15(2):. PubMed ID: 27323137
[TBL] [Abstract][Full Text] [Related]
15. Association between functional haplotypes of vascular endothelial growth factor and renal complications in Henoch-Schönlein purpura.
Rueda B; Perez-Armengol C; Lopez-Lopez S; Garcia-Porrua C; Martín J; Gonzalez-Gay MA
J Rheumatol; 2006 Jan; 33(1):69-73. PubMed ID: 16395752
[TBL] [Abstract][Full Text] [Related]
16. Polymorphism at codon 469 of the intercellular adhesion molecule-1 locus is associated with protection against severe gastrointestinal complications in Henoch-Schönlein purpura.
Amoli MM; Mattey DL; Calviño MC; Garcia-Porrua C; Thomson W; Hajeer AH; Ollier WE; Gonzalez-Gay MA
J Rheumatol; 2001 May; 28(5):1014-8. PubMed ID: 11361181
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. HLA class 1 associations in Henoch Schonlein purpura: increased and decreased frequencies.
Peru H; Soylemezoglu O; Gonen S; Cetinyurek A; Bakkaloğlu SA; Buyan N; Hasanoglu E
Clin Rheumatol; 2008 Jan; 27(1):5-10. PubMed ID: 17487448
[TBL] [Abstract][Full Text] [Related]
19. Association of endothelial nitric oxide synthase gene polymorphism with the risk of Henoch-Schönlein purpura/Henoch-Schönlein purpura nephritis.
Zhong W; Zhou TB; Jiang Z
Ren Fail; 2015 Apr; 37(3):372-6. PubMed ID: 25585947
[TBL] [Abstract][Full Text] [Related]
20. The association between transforming growth factor-beta gene promoter C-509T polymorphism and Chinese children with Henoch-Schönlein purpura.
Yang YH; Lai HJ; Kao CK; Lin YT; Chiang BL
Pediatr Nephrol; 2004 Sep; 19(9):972-5. PubMed ID: 15257453
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
