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Journal Abstract Search

147 related items for PubMed ID: 11031105

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  • 4. Evaluation of genetic variation and association in the matrix metalloproteinase 9 (MMP9) gene in ESRD patients.
    Hirakawa S, Lange EM, Colicigno CJ, Freedman BI, Rich SS, Bowden DW.
    Am J Kidney Dis; 2003 Jul; 42(1):133-42. PubMed ID: 12830465
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  • 5. Association of the tissue kallikrein gene promoter with ESRD and hypertension.
    Yu H, Song Q, Freedman BI, Chao J, Chao L, Rich SS, Bowden DW.
    Kidney Int; 2002 Mar; 61(3):1030-9. PubMed ID: 11849458
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  • 7. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
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  • 12. Chromosome 7p linkage and association study for diabetes related traits and type 2 diabetes in an African-American population enriched for nephropathy.
    Leak TS, Langefeld CD, Keene KL, Gallagher CJ, Lu L, Mychaleckyj JC, Rich SS, Freedman BI, Bowden DW, Sale MM.
    BMC Med Genet; 2010 Feb 08; 11():22. PubMed ID: 20144192
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  • 15. Structure of the murine fifth complement component (C5) gene. A large, highly interrupted gene with a variant donor splice site and organizational homology with the third and fourth complement component genes.
    Haviland DL, Haviland JC, Fleischer DT, Wetsel RA.
    J Biol Chem; 1991 Jun 25; 266(18):11818-25. PubMed ID: 1711041
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  • 16. Low prevalence of nonconservative mutations of serum and glucocorticoid-regulated kinase (SGK1) gene in hypertensive and renal patients.
    Trochen N, Ganapathipillai S, Ferrari P, Frey BM, Frey FJ.
    Nephrol Dial Transplant; 2004 Oct 25; 19(10):2499-504. PubMed ID: 15304560
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