74 related articles for article (PubMed ID: 21178826)
1. Linkage and association study of neurotrophins and their receptors as novel susceptibility genes for childhood IgA nephropathy.
Hahn WH; Suh JS; Cho BS
Pediatr Res; 2011 Apr; 69(4):299-305. PubMed ID: 21178826
[TBL] [Abstract][Full Text] [Related]
2. Neurotrophin serum concentrations and polymorphisms of neurotrophins and their receptors in children with asthma.
Szczepankiewicz A; Rachel M; Sobkowiak P; Kycler Z; Wojsyk-Banaszak I; Schöneich N; Szczawińska-Popłonyk A; Bręborowicz A
Respir Med; 2013 Jan; 107(1):30-6. PubMed ID: 23195334
[TBL] [Abstract][Full Text] [Related]
3. Search for genetic association between IgA nephropathy and candidate genes selected by function or by gene mapping at loci IGAN2 and IGAN3.
Bertinetto FE; Calafell F; Roggero S; Chidichimo R; Garino E; Marcuccio C; Coppo R; Scolari F; Frascá GM; Savoldi S; Schena FP; Amoroso A;
Nephrol Dial Transplant; 2012 Jun; 27(6):2328-37. PubMed ID: 22131235
[TBL] [Abstract][Full Text] [Related]
4. Association study of 10 genes encoding neurotrophic factors and their receptors in adult and child attention-deficit/hyperactivity disorder.
Ribasés M; Hervás A; Ramos-Quiroga JA; Bosch R; Bielsa A; Gastaminza X; Fernández-Anguiano M; Nogueira M; Gómez-Barros N; Valero S; Gratacòs M; Estivill X; Casas M; Cormand B; Bayés M
Biol Psychiatry; 2008 May; 63(10):935-45. PubMed ID: 18179783
[TBL] [Abstract][Full Text] [Related]
5. Polymorphisms of signal transducers and activators of transcription 1 and 4 (STAT1 and STAT4) contribute to progression of childhood IgA nephropathy.
Hahn WH; Suh JS; Cho SH; Cho BS; Kim SD
Cytokine; 2010 Apr; 50(1):69-74. PubMed ID: 20045654
[TBL] [Abstract][Full Text] [Related]
6. [Association of single nucleotide polymorphism of megsin gene with IgA nephropathy].
Wang ZH; Chen N; Pan XX; Ren H; Wang WM; Zhang W; Hao CL; Zhu J; Lu Y; Han B
Zhonghua Yi Xue Za Zhi; 2006 May; 86(19):1337-41. PubMed ID: 16796905
[TBL] [Abstract][Full Text] [Related]
7. Phosphodiesterase-5 gene (PDE5A) polymorphisms are associated with progression of childhood IgA nephropathy.
Hahn WH; Suh JS; Cho BS
Pediatr Nephrol; 2010 Sep; 25(9):1663-71. PubMed ID: 20563733
[TBL] [Abstract][Full Text] [Related]
8. Interleukin-1 cluster gene polymorphisms in childhood IgA nephropathy.
Hahn WH; Cho BS; Kim SD; Kim SK; Kang S
Pediatr Nephrol; 2009 Jul; 24(7):1329-36. PubMed ID: 19280228
[TBL] [Abstract][Full Text] [Related]
9. Extensive genotyping of the BDNF and NTRK2 genes define protective haplotypes against obsessive-compulsive disorder.
Alonso P; Gratacòs M; Menchón JM; Saiz-Ruiz J; Segalàs C; Baca-García E; Labad J; Fernández-Piqueras J; Real E; Vaquero C; Pérez M; Dolengevich H; González JR; Bayés M; de Cid R; Vallejo J; Estivill X
Biol Psychiatry; 2008 Mar; 63(6):619-28. PubMed ID: 17884018
[TBL] [Abstract][Full Text] [Related]
10. Linkage and association study of discoidin domain receptor 1 as a novel susceptibility gene for childhood IgA nephropathy.
Hahn WH; Suh JS; Cho BS; Kim SD
Int J Mol Med; 2010 May; 25(5):785-91. PubMed ID: 20372823
[TBL] [Abstract][Full Text] [Related]
11. Association of FOS-like antigen 1 promoter polymorphism with podocyte foot process effacement in immunoglobulin A nephropathy patients.
Park HJ; Kim JW; Cho BS; Chung JH
J Clin Lab Anal; 2014 Sep; 28(5):391-7. PubMed ID: 24652774
[TBL] [Abstract][Full Text] [Related]
12. Morphometric analysis of podocyte foot process effacement in IgA nephropathy and its association with proteinuria.
Choi SY; Suh KS; Choi DE; Lim BJ
Ultrastruct Pathol; 2010 Aug; 34(4):195-8. PubMed ID: 20594038
[TBL] [Abstract][Full Text] [Related]
13. Genetic variant of C1GalT1 contributes to the susceptibility to IgA nephropathy.
Pirulli D; Crovella S; Ulivi S; Zadro C; Bertok S; Rendine S; Scolari F; Foramitti M; Ravani P; Roccatello D; Savoldi S; Cerullo G; Lanzilotta SG; Bisceglia L; Zelante L; Floege J; Alexopoulos E; Kirmizis D; Ghiggeri GM; Frascà G; Schena FP; Amoroso A;
J Nephrol; 2009; 22(1):152-9. PubMed ID: 19229831
[TBL] [Abstract][Full Text] [Related]
14. Polymorphisms of insulin-like growth factor-1 (IGF-1) and IGF-1 receptor (IGF-1R) contribute to pathologic progression in childhood IgA nephropathy.
Hahn WH; Suh JS; Cho BS
Growth Factors; 2011 Feb; 29(1):8-13. PubMed ID: 21047277
[TBL] [Abstract][Full Text] [Related]
15. [Variable number of tandem repeats polymorphism of MUC20 is associated with the progression of IgA nephropathy].
Li GS; Zhang H; Lü JC; Hou P; Zhou Y; Ma XZ; Wang HY
Zhonghua Yi Xue Za Zhi; 2005 May; 85(19):1333-8. PubMed ID: 16029633
[TBL] [Abstract][Full Text] [Related]
16. Human trabecular meshwork cells secrete neurotrophins and express neurotrophin receptors (Trk).
Wordinger RJ; Lambert W; Agarwal R; Talati M; Clark AF
Invest Ophthalmol Vis Sci; 2000 Nov; 41(12):3833-41. PubMed ID: 11053283
[TBL] [Abstract][Full Text] [Related]
17. Variants of the ST6GALNAC2 promoter influence transcriptional activity and contribute to genetic susceptibility to IgA nephropathy.
Li GS; Zhu L; Zhang H; Lv JC; Ding JX; Zhao MH; Shen Y; Wang HY
Hum Mutat; 2007 Oct; 28(10):950-7. PubMed ID: 17480010
[TBL] [Abstract][Full Text] [Related]
18. Genetic effect of the NPHS2 gene variants on proteinuria in minimal change disease and immunoglobulin A nephropathy.
Zhu L; Yu L; Wang CD; Lv JC; Li GS; Zhang H; Wang HY
Nephrology (Carlton); 2009 Dec; 14(8):728-34. PubMed ID: 20025681
[TBL] [Abstract][Full Text] [Related]
19. Genetic polymorphisms in the promoter and 5' UTR region of the Fc alpha receptor (CD89) are not associated with a risk of IgA nephropathy.
Narita I; Goto S; Saito N; Sakatsume M; Jin S; Omori K; Gejyo F
J Hum Genet; 2001; 46(12):694-8. PubMed ID: 11776381
[TBL] [Abstract][Full Text] [Related]
20. Single-nucleotide polymorphisms in the class II region of the major histocompatibility complex in Japanese patients with immunoglobulin A nephropathy.
Akiyama F; Tanaka T; Yamada R; Ohnishi Y; Tsunoda T; Maeda S; Takei T; Obara W; Ito K; Honda K; Uchida K; Tsuchiya K; Nitta K; Yumura W; Nihei H; Ujiie T; Nagane Y; Miyano S; Suzuki Y; Fujioka T; Narita I; Gejyo F; Nakamura Y
J Hum Genet; 2002; 47(10):532-8. PubMed ID: 12376743
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]