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Journal Abstract Search


222 related items for PubMed ID: 18927121

  • 41. 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, European IgAN Consortium.
    J Nephrol; 2009; 22(1):152-9. PubMed ID: 19229831
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  • 43. In silico discrimination of single nucleotide polymorphisms and pathological mutations in human gene promoter regions by means of local DNA sequence context and regularity.
    Khan IA, Mort M, Buckland PR, O'Donovan MC, Cooper DN, Chuzhanova NA.
    In Silico Biol; 2006; 6(1-2):23-34. PubMed ID: 16789908
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  • 44. The association of MMP-9 and IL-18 gene promoter polymorphisms with gingivitis in adolescents.
    Vokurka J, Klapusová L, Pantuckova P, Kukletova M, Kukla L, Holla LI.
    Arch Oral Biol; 2009 Feb; 54(2):172-8. PubMed ID: 18930181
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  • 46. [Expression of MT1-MMP and its significance in rabbit VX2 tumor tissues after transarterial embolization with hydroxyapatite nanoparticles].
    Xu T, Chen XP, Guo YX, Li D, Lu L, Huan GZ, Zhang WG.
    Zhonghua Wai Ke Za Zhi; 2008 Apr 15; 46(8):606-9. PubMed ID: 18844058
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  • 48. [Class II human leukocyte antigens in minimal change nephrotic syndrome and focal segmental glomerulosclerosis--preliminary study].
    Krasowska-Kwiecień A, Sancewicz-Pach K, Pogan A.
    Pol Merkur Lekarski; 2001 Apr 15; 10(58):256-8. PubMed ID: 11434170
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  • 51. Single nucleotide polymorphism -799C/T in matrix metalloproteinase-8 promoter region in arterial disease.
    Pradhan-Palikhe P, Pussinen PJ, Vikatmaa P, Palikhe A, Kivimäki AS, Lepäntalo M, Salo T, Sorsa T.
    Innate Immun; 2012 Jun 15; 18(3):511-7. PubMed ID: 21994255
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  • 53. Influence of cytokine gene polymorphisms on focal segmental glomerulosclerosis.
    Bantis C, Heering PJ, Luther Y, Aker S, Kuhr N, Grabensee B, Ivens K.
    Am J Nephrol; 2004 Jun 15; 24(4):427-31. PubMed ID: 15308875
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  • 54. Effect of matrix metalloproteinase-3 functional SNP on serum matrix metalloproteinase-3 level and outcome measures in Japanese RA patients.
    Tsukahara S, Shinozaki M, Ikari K, Mochizuki T, Inoue E, Tomatsu T, Hara M, Yamanaka H, Kamatani N, Momohara S.
    Rheumatology (Oxford); 2008 Jan 15; 47(1):41-4. PubMed ID: 18077489
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  • 57. Vascular endothelial growth factor gene polymorphisms as prognostic markers for ocular manifestations in pseudoxanthoma elasticum.
    Zarbock R, Hendig D, Szliska C, Kleesiek K, Götting C.
    Hum Mol Genet; 2009 Sep 01; 18(17):3344-51. PubMed ID: 19483196
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  • 59. Focal segmental glomerular sclerosis in three generations of a single family.
    Sanchez Tomero JA, Arrieta J, Alguacil A, Alonso A, Macias JF, Tabernero JM.
    Int J Pediatr Nephrol; 1985 Sep 01; 6(3):199-204. PubMed ID: 3902692
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