85 related articles for article (PubMed ID: 20540633)
1. Lack of association between transient receptor potential cation channel 6 polymorphisms and primary membranous glomerulonephritis.
Chen WC; Chen SY; Chen CH; Chen HY; Lin YW; Ho TJ; Huang YC; Shen JL; Tsai FJ; Chen YH
Ren Fail; 2010 Jul; 32(6):666-72. PubMed ID: 20540633
[TBL] [Abstract][Full Text] [Related]
2. Association between genetic polymorphisms of the NPHS1 gene and membranous glomerulonephritis in the Taiwanese population.
Lo WY; Chen SY; Wang HJ; Shih HC; Chen CH; Tsai CH; Tsai FJ
Clin Chim Acta; 2010 May; 411(9-10):714-8. PubMed ID: 20138859
[TBL] [Abstract][Full Text] [Related]
3. Association of STAT4 polymorphisms with susceptibility to primary membranous glomerulonephritis and renal failure.
Chen SY; Chen CH; Huang YC; Chan CJ; Hsieh YY; Yu MC; Tsai CH; Tsai FJ
Clin Chim Acta; 2011 Oct; 412(21-22):1899-904. PubMed ID: 21740896
[TBL] [Abstract][Full Text] [Related]
4. Impact of plasminogen activator inhibitor-1 gene polymorphisms on primary membranous nephropathy.
Chen CH; Shu KH; Wen MC; Chen KJ; Cheng CH; Lian JD; Wu MJ; Yu TM; Tsai FJ
Nephrol Dial Transplant; 2008 Oct; 23(10):3166-73. PubMed ID: 18495745
[TBL] [Abstract][Full Text] [Related]
5. TRPC6 single nucleotide polymorphisms and progression of idiopathic membranous nephropathy.
Hofstra JM; Coenen MJ; Schijvenaars MM; Berden JH; van der Vlag J; Hoefsloot LH; Knoers NV; Wetzels JF; Nijenhuis T
PLoS One; 2014; 9(7):e102065. PubMed ID: 25019165
[TBL] [Abstract][Full Text] [Related]
6. TRPC6 gene variants in Turkish children with steroid-resistant nephrotic syndrome.
Mir S; Yavascan O; Berdeli A; Sozeri B
Nephrol Dial Transplant; 2012 Jan; 27(1):205-9. PubMed ID: 21511817
[TBL] [Abstract][Full Text] [Related]
7. Association of GABA(B)R1 receptor gene polymorphism with obstructive sleep apnea syndrome.
Bayazit YA; Yilmaz M; Kokturk O; Erdal ME; Ciftci T; Gokdogan T; Kemaloglu Y; Ileri F
ORL J Otorhinolaryngol Relat Spec; 2007; 69(3):190-7. PubMed ID: 17264536
[TBL] [Abstract][Full Text] [Related]
8. Clinical and morphological prognostic factors in membranous nephropathy: significance of focal segmental glomerulosclerosis.
Dumoulin A; Hill GS; Montseny JJ; Meyrier A
Am J Kidney Dis; 2003 Jan; 41(1):38-48. PubMed ID: 12500220
[TBL] [Abstract][Full Text] [Related]
9. Primary IgA nephropathy is more severe in TGF-beta1 high secretor patients.
Brezzi B; Del Prete D; Lupo A; Magistroni R; Gomez-Lira M; Bernich P; Anglani F; Mezzabotta F; Turco A; Furci L; Ceol M; Antonucci F; Abaterusso C; Bonfante L; D'Angelo A; Albertazzi A; Gambaro G
J Nephrol; 2009; 22(6):747-59. PubMed ID: 19967654
[TBL] [Abstract][Full Text] [Related]
10. Effects of genetic polymorphisms of the renin-angiotensin system in children with nephrotic syndrome.
Tabel Y; Berdeli A; Mir S; Serdaroğlu E; Yilmaz E
J Renin Angiotensin Aldosterone Syst; 2005 Dec; 6(3):138-44. PubMed ID: 16525944
[TBL] [Abstract][Full Text] [Related]
11. Demographic and Clinicopathologic features of membranous glomerulonephritis.
Azad NS; Muzaffar S; Pervez S; Ahmed A; Rabbani A; Ali A
J Coll Physicians Surg Pak; 2004 Jan; 14(1):35-8. PubMed ID: 14764259
[TBL] [Abstract][Full Text] [Related]
12. New TRPC6 gain-of-function mutation in a non-consanguineous Dutch family with late-onset focal segmental glomerulosclerosis.
Hofstra JM; Lainez S; van Kuijk WH; Schoots J; Baltissen MP; Hoefsloot LH; Knoers NV; Berden JH; Bindels RJ; van der Vlag J; Hoenderop JG; Wetzels JF; Nijenhuis T
Nephrol Dial Transplant; 2013 Jul; 28(7):1830-8. PubMed ID: 23291369
[TBL] [Abstract][Full Text] [Related]
13. Impact of de novo membranous glomerulonephritis on the clinical course after kidney transplantation.
Schwarz A; Krause PH; Offermann G; Keller F
Transplantation; 1994 Sep; 58(6):650-4. PubMed ID: 7940683
[TBL] [Abstract][Full Text] [Related]
14. Molecular and clinical analysis of TRPC6 and AGTR1 genes in patients with pulmonary arterial hypertension.
Pousada G; Baloira A; Valverde D
Orphanet J Rare Dis; 2015 Jan; 10():1. PubMed ID: 25603901
[TBL] [Abstract][Full Text] [Related]
15. CD20-positive infiltrates in human membranous glomerulonephritis.
Cohen CD; Calvaresi N; Armelloni S; Schmid H; Henger A; Ott U; Rastaldi MP; Kretzler M
J Nephrol; 2005; 18(3):328-33. PubMed ID: 16013025
[TBL] [Abstract][Full Text] [Related]
16. VEGF -460 genotype plays an important role in progression to chronic kidney disease stage 5.
Summers AM; Coupes BM; Brennan MF; Ralph SA; Short CD; Brenchley PE
Nephrol Dial Transplant; 2005 Nov; 20(11):2427-32. PubMed ID: 16046504
[TBL] [Abstract][Full Text] [Related]
17. Single nucleotide polymorphisms in the phospholipase A2 receptor gene are associated with genetic susceptibility to idiopathic membranous nephropathy.
Kim S; Chin HJ; Na KY; Kim S; Oh J; Chung W; Noh JW; Lee YK; Cho JT; Lee EK; Chae DW;
Nephron Clin Pract; 2011; 117(3):c253-8. PubMed ID: 20805699
[TBL] [Abstract][Full Text] [Related]
18. TRPC6 mutational analysis in a large cohort of patients with focal segmental glomerulosclerosis.
Santín S; Ars E; Rossetti S; Salido E; Silva I; García-Maset R; Giménez I; Ruíz P; Mendizábal S; Luciano Nieto J; Peña A; Camacho JA; Fraga G; Cobo MA; Bernis C; Ortiz A; de Pablos AL; Sánchez-Moreno A; Pintos G; Mirapeix E; Fernández-Llama P; Ballarín J; Torra R; ; Zamora I; López-Hellin J; Madrid A; Ventura C; Vilalta R; Espinosa L; García C; Melgosa M; Navarro M; Giménez A; Cots JV; Alexandra S; Caramelo C; Egido J; San José MD; de la Cerda F; Sala P; Raspall F; Vila A; Daza AM; Vázquez M; Ecija JL; Espinosa M; Justa ML; Poveda R; Aparicio C; Rosell J; Muley R; Montenegro J; González D; Hidalgo E; de Frutos DB; Trillo E; Gracia S; de los Ríos FJ
Nephrol Dial Transplant; 2009 Oct; 24(10):3089-96. PubMed ID: 19458060
[TBL] [Abstract][Full Text] [Related]
19. Focal segmental glomerulosclerosis after membranous glomerulonephritis in remission: temporal diversity of glomerulopathy after bone marrow transplantation.
Chan GS; Chim S; Fan YS; Chan KW
Hum Pathol; 2006 Dec; 37(12):1607-10. PubMed ID: 17020780
[TBL] [Abstract][Full Text] [Related]
20. Methylenetetrahydrofolate reductase gene polymorphisms c.677C/T and c.1298A/C are not associated with open angle glaucoma.
Mabuchi F; Tang S; Kashiwagi K; Yamagata Z; Iijima H; Tsukahara S
Mol Vis; 2006 Jul; 12():735-9. PubMed ID: 16862068
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
