159 related articles for article (PubMed ID: 25163389)
21. [Uteroglobin G38A polymorphism is associated with the progression of IgA nephropathy in Chinese patients].
Lü JC; Zhang H; Chen YQ; Liu G; Wang HY
Zhonghua Nei Ke Za Zhi; 2004 Jan; 43(1):37-40. PubMed ID: 14990020
[TBL] [Abstract][Full Text] [Related]
22. Genetic polymorphism of C3 and Bf in IgA nephropathy.
Rambausek M; van den Wall Bake AW; Schumacher-Ach R; Spitzenberg R; Rother U; van Es LA; Ritz E
Nephrol Dial Transplant; 1987; 2(4):208-11. PubMed ID: 3118258
[TBL] [Abstract][Full Text] [Related]
23. Influence of cytokine gene polymorphisms on IgA nephropathy.
Bantis C; Heering P; Aker S; Kuhr N; Grabensee B; Ivens K
Ren Fail; 2008; 30(2):135-40. PubMed ID: 18300111
[TBL] [Abstract][Full Text] [Related]
24. Genetic polymorphism of vascular endothelial growth factor: impact on progression of IgA nephropathy.
Chow KM; Szeto CC; Lai FM; Poon P; Wong TY; Li PK
Ren Fail; 2006; 28(1):15-20. PubMed ID: 16526314
[TBL] [Abstract][Full Text] [Related]
25. [The association of single nucleotide P-selectin gene polymorphism with IgA nephropathy].
Wang ZH; Wang WM; Zhou T; Chen XN; Pan XX; Zhu J; Lu Y; Han B; Chen N
Zhonghua Nei Ke Za Zhi; 2006 Jul; 45(7):559-64. PubMed ID: 17074110
[TBL] [Abstract][Full Text] [Related]
26. Polymorphism of angiotensin converting enzyme, angiotensinogen, and angiotensin II type 1 receptor genes and end-stage renal failure in IgA nephropathy: IGARAS--a study of 274 Men.
Frimat L; Philippe C; Maghakian MN; Jonveaux P; DE Ligny BH; Guillemin F; Kessler M
J Am Soc Nephrol; 2000 Nov; 11(11):2062-2067. PubMed ID: 11053482
[TBL] [Abstract][Full Text] [Related]
27. A meta-analysis of the association between angiotensin-converting enzyme insertion/deletion gene polymorphism and end-stage renal disease risk in IgA nephropathy patients.
Zhou TB; Yin SS; Liang R
J Renin Angiotensin Aldosterone Syst; 2013 Sep; 14(3):235-41. PubMed ID: 23060471
[TBL] [Abstract][Full Text] [Related]
28. CC-chemokine receptor five gene polymorphism in primary IgA nephropathy: the 32 bp deletion allele is associated with late progression to end-stage renal failure with dialysis.
Berthoux FC; Berthoux P; Mariat C; Thibaudin L; Afiani A; Linossier MT
Kidney Int; 2006 Feb; 69(3):565-72. PubMed ID: 16395252
[TBL] [Abstract][Full Text] [Related]
29. Urinary uromodulin excretion predicts progression of chronic kidney disease resulting from IgA nephropathy.
Zhou J; Chen Y; Liu Y; Shi S; Wang S; Li X; Zhang H; Wang H
PLoS One; 2013; 8(8):e71023. PubMed ID: 23990922
[TBL] [Abstract][Full Text] [Related]
30. A-20C angiotensinogen gene polymorphism and proteinuria in childhood IgA nephropathy.
Nakanishi K; Sako M; Yata N; Aoyagi N; Nozu K; Tanaka R; Iijima K; Yoshikawa N
Pediatr Nephrol; 2004 Feb; 19(2):144-7. PubMed ID: 14648325
[TBL] [Abstract][Full Text] [Related]
31. A family-based association study of megsin A23167G polymorphism with susceptibility and progression of IgA nephropathy in a Chinese population.
Xia YF; Huang S; Li X; Yang N; Huang J; Xue C; Zhang M; Leung JC; Lam MF; Li J
Clin Nephrol; 2006 Mar; 65(3):153-9. PubMed ID: 16550745
[TBL] [Abstract][Full Text] [Related]
32. Role of uteroglobin G38A polymorphism in the progression of IgA nephropathy in Japanese patients.
Narita I; Saito N; Goto S; Jin S; Omori K; Sakatsume M; Gejyo F
Kidney Int; 2002 May; 61(5):1853-8. PubMed ID: 11967037
[TBL] [Abstract][Full Text] [Related]
33. Kidney Failure Risk Prediction Equations in IgA Nephropathy: A Multicenter Risk Assessment Study in Chinese Patients.
Xie J; Lv J; Wang W; Li G; Liu Z; Chen H; Xu F; Sun J; Ouyang Y; Zhang X; Yang M; Shi M; Zhang W; Ren H; Kiryluk K; Zhang H; Chen N
Am J Kidney Dis; 2018 Sep; 72(3):371-380. PubMed ID: 29555434
[TBL] [Abstract][Full Text] [Related]
34. Study of Uromodulin Gene Polymorphism in Egyptian Patients with End-Stage Renal Disease.
Abdelsalam M; Motawea M; Kyrillos F; Abdel-Razik A; Zaki MES; Abdel-Wahab A
Saudi J Kidney Dis Transpl; 2021; 32(1):157-162. PubMed ID: 34145125
[TBL] [Abstract][Full Text] [Related]
35. Meta-analysis demonstrates association of the TGF-β1 gene -C509T polymorphism with susceptibility to IgA nephropathy in European but not in Asian populations.
Wang H; Li P; Feng ZC
Genet Mol Res; 2013 Feb; 12(1):434-42. PubMed ID: 23420368
[TBL] [Abstract][Full Text] [Related]
36. Clinical Heterogeneity in Familial IgA Nephropathy.
Fennelly NK; Kennedy C; Jenkinson AC; Connaughton DM; Stapleton C; Dorman AM; Doyle B; Conlon PJ
Nephron; 2018; 139(1):63-69. PubMed ID: 29402819
[TBL] [Abstract][Full Text] [Related]
37. Non-diabetic end-stage renal disease in Saudis associated with polymorphism of MYH9 gene but not UMOD gene.
Adam KM; Mohammed AM; Elamin AA
Medicine (Baltimore); 2020 Jan; 99(3):e18722. PubMed ID: 32011449
[TBL] [Abstract][Full Text] [Related]
38. The pathogenetic aspects and gene polymorphisms of IgA nephropathy.
Maixnerová D; Merta M; Reiterová J; Stekrová J; Rysavá R; Obeidová H; Tesar V
Prague Med Rep; 2006; 107(2):171-88. PubMed ID: 17066738
[TBL] [Abstract][Full Text] [Related]
39. Influence of the endothelial nitric oxide synthase polymorphism on the progression of autosomal dominant polycystic kidney disease and IgA nephropathy.
Merta M; Reiterová J; Tesar V; Stekrová J; Viklický O
Ren Fail; 2002 Jul; 24(4):467-75. PubMed ID: 12212826
[TBL] [Abstract][Full Text] [Related]
40. Common genetic variants of the human uromodulin gene regulate transcription and predict plasma uric acid levels.
Han J; Liu Y; Rao F; Nievergelt CM; O'Connor DT; Wang X; Liu L; Bu D; Liang Y; Wang F; Zhang L; Zhang H; Chen Y; Wang H
Kidney Int; 2013 Apr; 83(4):733-40. PubMed ID: 23344472
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
