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Journal Abstract Search

104 related items for PubMed ID: 10023641

  • 1. Evaluation of markers on human chromosome 10, including the homologue of the rodent Rf-1 gene, for linkage to ESRD in black patients.
    Yu H, Sale M, Rich SS, Spray BJ, Roh BH, Bowden DW, Freedman BI.
    Am J Kidney Dis; 1999 Feb; 33(2):294-300. PubMed ID: 10023641
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  • 2. Linkage heterogeneity of end-stage renal disease on human chromosome 10.
    Freedman BI, Rich SS, Yu H, Roh BH, Bowden DW.
    Kidney Int; 2002 Sep; 62(3):770-4. PubMed ID: 12164858
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  • 4. Genetic analysis of nitric oxide and endothelin in end-stage renal disease.
    Freedman BI, Yu H, Anderson PJ, Roh BH, Rich SS, Bowden DW.
    Nephrol Dial Transplant; 2000 Nov; 15(11):1794-800. PubMed ID: 11071967
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  • 5. Identification of human plasma kallikrein gene polymorphisms and evaluation of their role in end-stage renal disease.
    Yu H, Bowden DW, Spray BJ, Rich SS, Freedman BI.
    Hypertension; 1998 Apr; 31(4):906-11. PubMed ID: 9535413
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  • 7. Linkage analysis of candidate loci for end-stage renal disease due to diabetic nephropathy.
    Iyengar SK, Fox KA, Schachere M, Manzoor F, Slaughter ME, Covic AM, Orloff SM, Hayden PS, Olson JM, Schelling JR, Sedor JR.
    J Am Soc Nephrol; 2003 Jul; 14(7 Suppl 2):S195-201. PubMed ID: 12819328
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  • 8. Linkage analysis between loci in the renin-angiotensin axis and end-stage renal disease in African Americans.
    Yu H, Bowden DW, Spray BJ, Rich SS, Freedman BI.
    J Am Soc Nephrol; 1996 Dec; 7(12):2559-64. PubMed ID: 8989734
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  • 9. Genomic structure of the human plasma prekallikrein gene, identification of allelic variants, and analysis in end-stage renal disease.
    Yu H, Anderson PJ, Freedman BI, Rich SS, Bowden DW.
    Genomics; 2000 Oct 15; 69(2):225-34. PubMed ID: 11031105
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  • 11. Candidate gene analysis in African Americans with renal failure.
    Buckalew VM, Freedman BI.
    Ren Fail; 1999 Oct 15; 21(3-4):403-7. PubMed ID: 10416219
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  • 12. Susceptibility locus for Alzheimer's disease on chromosome 10.
    Myers A, Holmans P, Marshall H, Kwon J, Meyer D, Ramic D, Shears S, Booth J, DeVrieze FW, Crook R, Hamshere M, Abraham R, Tunstall N, Rice F, Carty S, Lillystone S, Kehoe P, Rudrasingham V, Jones L, Lovestone S, Perez-Tur J, Williams J, Owen MJ, Hardy J, Goate AM.
    Science; 2000 Dec 22; 290(5500):2304-5. PubMed ID: 11125144
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  • 14. Racial variation in autosomal dominant polycystic kidney disease.
    Freedman BI, Soucie JM, Chapman A, Krisher J, McClellan WM.
    Am J Kidney Dis; 2000 Jan 22; 35(1):35-9. PubMed ID: 10620541
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  • 19. Mitochondrial DNA mutations in black Americans with hypertension-associated end-stage renal disease.
    Watson B, Khan MA, Desmond RA, Bergman S.
    Am J Kidney Dis; 2001 Sep 22; 38(3):529-36. PubMed ID: 11532685
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  • 20. MYH9 is associated with nondiabetic end-stage renal disease in African Americans.
    Kao WH, Klag MJ, Meoni LA, Reich D, Berthier-Schaad Y, Li M, Coresh J, Patterson N, Tandon A, Powe NR, Fink NE, Sadler JH, Weir MR, Abboud HE, Adler SG, Divers J, Iyengar SK, Freedman BI, Kimmel PL, Knowler WC, Kohn OF, Kramp K, Leehey DJ, Nicholas SB, Pahl MV, Schelling JR, Sedor JR, Thornley-Brown D, Winkler CA, Smith MW, Parekh RS, Family Investigation of Nephropathy and Diabetes Research Group.
    Nat Genet; 2008 Oct 22; 40(10):1185-92. PubMed ID: 18794854
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