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 *

71 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]
    of 4.