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Journal Abstract Search

242 related items for PubMed ID: 27197912

  • 1. Association Analysis of the Cubilin (CUBN) and Megalin (LRP2) Genes with ESRD in African Americans.
    Ma J, Guan M, Bowden DW, Ng MCY, Hicks PJ, Lea JP, Ma L, Gao C, Palmer ND, Freedman BI.
    Clin J Am Soc Nephrol; 2016 Jun 06; 11(6):1034-1043. PubMed ID: 27197912
    [Abstract] [Full Text] [Related]

  • 2. Cubilin Single Nucleotide Polymorphism Variants are Associated with Macroangiopathy While a Matrix Metalloproteinase-9 Single Nucleotide Polymorphism Flip-Flop may Indicate Susceptibility of Diabetic Nephropathy in Type-2 Diabetic Patients.
    Albert C, Kube J, Albert A, Schanze D, Zenker M, Mertens PR.
    Nephron; 2019 Jun 06; 141(3):156-165. PubMed ID: 30557881
    [Abstract] [Full Text] [Related]

  • 3. Coding variants in nephrin (NPHS1) and susceptibility to nephropathy in African Americans.
    Bonomo JA, Ng MC, Palmer ND, Keaton JM, Larsen CP, Hicks PJ, T2D-GENES Consortium, Langefeld CD, Freedman BI, Bowden DW.
    Clin J Am Soc Nephrol; 2014 Aug 07; 9(8):1434-40. PubMed ID: 24948143
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Analysis of coding variants identified from exome sequencing resources for association with diabetic and non-diabetic nephropathy in African Americans.
    Bailey JNC, Palmer ND, Ng MCY, Bonomo JA, Hicks PJ, Hester JM, Langefeld CD, Freedman BI, Bowden DW.
    Hum Genet; 2014 Jun 08; 133(6):769-779. PubMed ID: 24385048
    [Abstract] [Full Text] [Related]

  • 6. A genome-wide association study for diabetic nephropathy genes in African Americans.
    McDonough CW, Palmer ND, Hicks PJ, Roh BH, An SS, Cooke JN, Hester JM, Wing MR, Bostrom MA, Rudock ME, Lewis JP, Talbert ME, Blevins RA, Lu L, Ng MC, Sale MM, Divers J, Langefeld CD, Freedman BI, Bowden DW.
    Kidney Int; 2011 Mar 08; 79(5):563-72. PubMed ID: 21150874
    [Abstract] [Full Text] [Related]

  • 7. Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans.
    Freedman BI, Langefeld CD, Lu L, Divers J, Comeau ME, Kopp JB, Winkler CA, Nelson GW, Johnson RC, Palmer ND, Hicks PJ, Bostrom MA, Cooke JN, McDonough CW, Bowden DW.
    PLoS Genet; 2011 Jun 08; 7(6):e1002150. PubMed ID: 21698141
    [Abstract] [Full Text] [Related]

  • 8. Polymorphisms in LRP2 and CUBN genes and their association with serum vitamin D levels and sleep apnea.
    Anatolou D, Steiropoulos P, Zissimopoulos A, Chadia K, Archontogeorgis K, Kolios G, Manolopoulos VG, Ragia G.
    Sleep Breath; 2024 May 08; 28(2):959-966. PubMed ID: 38008818
    [Abstract] [Full Text] [Related]

  • 9. Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD.
    Freedman BI, Hicks PJ, Bostrom MA, Comeau ME, Divers J, Bleyer AJ, Kopp JB, Winkler CA, Nelson GW, Langefeld CD, Bowden DW.
    Nephrol Dial Transplant; 2009 Nov 08; 24(11):3366-71. PubMed ID: 19567477
    [Abstract] [Full Text] [Related]

  • 10. A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria.
    Ahluwalia TS, Schulz CA, Waage J, Skaaby T, Sandholm N, van Zuydam N, Charmet R, Bork-Jensen J, Almgren P, Thuesen BH, Bedin M, Brandslund I, Christensen CK, Linneberg A, Ahlqvist E, Groop PH, Hadjadj S, Tregouet DA, Jørgensen ME, Grarup N, Pedersen O, Simons M, Groop L, Orho-Melander M, McCarthy MI, Melander O, Rossing P, Kilpeläinen TO, Hansen T.
    Diabetologia; 2019 Feb 08; 62(2):292-305. PubMed ID: 30547231
    [Abstract] [Full Text] [Related]

  • 11. Relevance of the ACTN4 gene in African-Americans with non-diabetic end-stage renal disease.
    Bostrom MA, Perlegas P, Lu L, Hicks PJ, Hawkins G, Ng MC, Langefeld CD, Freedman BI, Bowden DW.
    Am J Nephrol; 2012 Feb 08; 36(3):252-60. PubMed ID: 22965004
    [Abstract] [Full Text] [Related]

  • 12. Sickle cell trait is not independently associated with susceptibility to end-stage renal disease in African Americans.
    Hicks PJ, Langefeld CD, Lu L, Bleyer AJ, Divers J, Nachman PH, Derebail VK, Bowden DW, Freedman BI.
    Kidney Int; 2011 Dec 08; 80(12):1339-43. PubMed ID: 21849968
    [Abstract] [Full Text] [Related]

  • 13. CUBN as a novel locus for end-stage renal disease: insights from renal transplantation.
    Reznichenko A, Snieder H, van den Born J, de Borst MH, Damman J, van Dijk MC, van Goor H, Hepkema BG, Hillebrands JL, Leuvenink HG, Niesing J, Bakker SJ, Seelen M, Navis G, REGaTTA (REnal GeneTics TrAnsplantation) Groningen group.
    PLoS One; 2012 Dec 08; 7(5):e36512. PubMed ID: 22574174
    [Abstract] [Full Text] [Related]

  • 14. Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans.
    Uglebjerg N, Ahmadizar F, Aly DM, Cañadas-Garre M, Hill C, Naber A, Oddsson A, Singh SS, Smyth L, Trégouët DA, Chaker L, Ghanbari M, Steinthorsdottir V, Ahlqvist E, Hadjadj S, Van Hoek M, Kavousi M, McKnight AJ, Sijbrands EJ, Stefansson K, Simons M, Rossing P, Ahluwalia TS.
    Front Endocrinol (Lausanne); 2023 Dec 08; 14():1081741. PubMed ID: 36926036
    [Abstract] [Full Text] [Related]

  • 15. Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with nondiabetic nephropathy than strong APOL1-second gene interactions.
    Langefeld CD, Comeau ME, Ng MCY, Guan M, Dimitrov L, Mudgal P, Spainhour MH, Julian BA, Edberg JC, Croker JA, Divers J, Hicks PJ, Bowden DW, Chan GC, Ma L, Palmer ND, Kimberly RP, Freedman BI.
    Kidney Int; 2018 Sep 08; 94(3):599-607. PubMed ID: 29885931
    [Abstract] [Full Text] [Related]

  • 16. Association Analysis of the Reticulon 1 Gene in End-Stage Kidney Disease.
    Bonomo JA, Palmer ND, He JC, Fan Y, Hicks PJ, Lea JP, Okusa MD, Bowden DW, Freedman BI.
    Am J Nephrol; 2015 Sep 08; 42(4):259-64. PubMed ID: 26496126
    [Abstract] [Full Text] [Related]

  • 17. Investigation of the estrogen receptor-alpha gene with type 2 diabetes and/or nephropathy in African-American and European-American populations.
    Gallagher CJ, Keene KL, Mychaleckyj JC, Langefeld CD, Hirschhorn JN, Henderson BE, Gordon CJ, Freedman BI, Rich SS, Bowden DW, Sale MM.
    Diabetes; 2007 Mar 08; 56(3):675-84. PubMed ID: 17327435
    [Abstract] [Full Text] [Related]

  • 18. Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy.
    Bostrom MA, Kao WH, Li M, Abboud HE, Adler SG, Iyengar SK, Kimmel PL, Hanson RL, Nicholas SB, Rasooly RS, Sedor JR, Coresh J, Kohn OF, Leehey DJ, Thornley-Brown D, Bottinger EP, Lipkowitz MS, Meoni LA, Klag MJ, Lu L, Hicks PJ, Langefeld CD, Parekh RS, Bowden DW, Freedman BI, Family Investigation of Nephropathy and Diabetes (FIND) Research Group.
    Am J Kidney Dis; 2012 Feb 08; 59(2):210-21. PubMed ID: 22119407
    [Abstract] [Full Text] [Related]

  • 19. APOL1 renal-risk genotypes associate with longer hemodialysis survival in prevalent nondiabetic African American patients with end-stage renal disease.
    Ma L, Langefeld CD, Comeau ME, Bonomo JA, Rocco MV, Burkart JM, Divers J, Palmer ND, Hicks PJ, Bowden DW, Lea JP, Krisher JO, Clay MJ, Freedman BI.
    Kidney Int; 2016 Aug 08; 90(2):389-395. PubMed ID: 27157696
    [Abstract] [Full Text] [Related]

  • 20. The ras responsive transcription factor RREB1 is a novel candidate gene for type 2 diabetes associated end-stage kidney disease.
    Bonomo JA, Guan M, Ng MC, Palmer ND, Hicks PJ, Keaton JM, Lea JP, Langefeld CD, Freedman BI, Bowden DW.
    Hum Mol Genet; 2014 Dec 15; 23(24):6441-7. PubMed ID: 25027322
    [Abstract] [Full Text] [Related]

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