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Results: 1 to 20 of 113

1.

Genetics of focal segmental glomerulosclerosis and human immunodeficiency virus-associated collapsing glomerulopathy: the role of MYH9 genetic variation.

Winkler CA, Nelson G, Oleksyk TK, Nava MB, Kopp JB.

Semin Nephrol. 2010 Mar;30(2):111-25. doi: 10.1016/j.semnephrol.2010.01.003. Review.

PMID:
20347641
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

MYH9 genetic variants associated with glomerular disease: what is the role for genetic testing?

Kopp JB, Winkler CA, Nelson GW.

Semin Nephrol. 2010 Jul;30(4):409-17. doi: 10.1016/j.semnephrol.2010.06.007.

PMID:
20807613
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.

Tzur S, Rosset S, Shemer R, Yudkovsky G, Selig S, Tarekegn A, Bekele E, Bradman N, Wasser WG, Behar DM, Skorecki K.

Hum Genet. 2010 Sep;128(3):345-50. doi: 10.1007/s00439-010-0861-0. Epub 2010 Jul 16.

PMID:
20635188
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Coincident idiopathic focal segmental glomerulosclerosis collapsing variant and diabetic nephropathy in an African American homozygous for MYH9 risk variants.

Gopalakrishnan I, Iskandar SS, Daeihagh P, Divers J, Langefeld CD, Bowden DW, Hicks PJ, Rocco MV, Freedman BI.

Hum Pathol. 2011 Feb;42(2):291-4. doi: 10.1016/j.humpath.2010.07.016. Epub 2010 Nov 13.

PMID:
21074826
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Is collapsing C1q nephropathy another MYH9-associated kidney disease? A case report.

Reeves-Daniel AM, Iskandar SS, Bowden DW, Bostrom MA, Hicks PJ, Comeau ME, Langefeld CD, Freedman BI.

Am J Kidney Dis. 2010 May;55(5):e21-4. doi: 10.1053/j.ajkd.2009.10.060. Epub 2010 Jan 29.

PMID:
20116156
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis.

Kopp JB, Smith MW, Nelson GW, Johnson RC, Freedman BI, Bowden DW, Oleksyk T, McKenzie LM, Kajiyama H, Ahuja TS, Berns JS, Briggs W, Cho ME, Dart RA, Kimmel PL, Korbet SM, Michel DM, Mokrzycki MH, Schelling JR, Simon E, Trachtman H, Vlahov D, Winkler CA.

Nat Genet. 2008 Oct;40(10):1175-84. doi: 10.1038/ng.226. Epub 2008 Sep 14.

PMID:
18794856
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.

Nelson GW, Freedman BI, Bowden DW, Langefeld CD, An P, Hicks PJ, Bostrom MA, Johnson RC, Kopp JB, Winkler CA.

Hum Mol Genet. 2010 May 1;19(9):1805-15. doi: 10.1093/hmg/ddq039. Epub 2010 Feb 2.

PMID:
20124285
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans.

Freedman BI, Kopp JB, Langefeld CD, Genovese G, Friedman DJ, Nelson GW, Winkler CA, Bowden DW, Pollak MR.

J Am Soc Nephrol. 2010 Sep;21(9):1422-6. doi: 10.1681/ASN.2010070730. Epub 2010 Aug 5. Review.

PMID:
20688934
[PubMed - indexed for MEDLINE]
Free Article
9.

Podocyte-specific deletion of Myh9 encoding nonmuscle myosin heavy chain 2A predisposes mice to glomerulopathy.

Johnstone DB, Zhang J, George B, Léon C, Gachet C, Wong H, Parekh R, Holzman LB.

Mol Cell Biol. 2011 May;31(10):2162-70. doi: 10.1128/MCB.05234-11. Epub 2011 Mar 14.

PMID:
21402784
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9.

Genovese G, Tonna SJ, Knob AU, Appel GB, Katz A, Bernhardy AJ, Needham AW, Lazarus R, Pollak MR.

Kidney Int. 2010 Oct;78(7):698-704. doi: 10.1038/ki.2010.251. Epub 2010 Jul 28.

PMID:
20668430
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Susceptibility genes in common complex kidney disease.

Divers J, Freedman BI.

Curr Opin Nephrol Hypertens. 2010 Jan;19(1):79-84. doi: 10.1097/MNH.0b013e3283331e50. Review.

PMID:
19838113
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

APOL1 variants increase risk for FSGS and HIVAN but not IgA nephropathy.

Papeta N, Kiryluk K, Patel A, Sterken R, Kacak N, Snyder HJ, Imus PH, Mhatre AN, Lawani AK, Julian BA, Wyatt RJ, Novak J, Wyatt CM, Ross MJ, Winston JA, Klotman ME, Cohen DJ, Appel GB, D'Agati VD, Klotman PE, Gharavi AG.

J Am Soc Nephrol. 2011 Nov;22(11):1991-6. doi: 10.1681/ASN.2011040434. Epub 2011 Oct 13.

PMID:
21997397
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

The spectrum of MYH9-associated nephropathy.

Bostrom MA, Freedman BI.

Clin J Am Soc Nephrol. 2010 Jun;5(6):1107-13. doi: 10.2215/CJN.08721209. Epub 2010 Mar 18. Review.

PMID:
20299374
[PubMed - indexed for MEDLINE]
Free Article
14.

Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans.

Freedman BI, Hicks PJ, Bostrom MA, Cunningham ME, Liu Y, Divers J, Kopp JB, Winkler CA, Nelson GW, Langefeld CD, Bowden DW.

Kidney Int. 2009 Apr;75(7):736-45. doi: 10.1038/ki.2008.701. Epub 2009 Jan 28.

PMID:
19177153
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

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;24(11):3366-71. doi: 10.1093/ndt/gfp316. Epub 2009 Jun 30.

PMID:
19567477
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study.

Freedman BI, Kopp JB, Winkler CA, Nelson GW, Rao DC, Eckfeldt JH, Leppert MF, Hicks PJ, Divers J, Langefeld CD, Hunt SC.

Am J Nephrol. 2009;29(6):626-32. doi: 10.1159/000194791. Epub 2009 Jan 20.

PMID:
19153477
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

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;40(10):1185-92. doi: 10.1038/ng.232. Epub 2008 Sep 14.

PMID:
18794854
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans.

Cooke JN, Bostrom MA, Hicks PJ, Ng MC, Hellwege JN, Comeau ME, Divers J, Langefeld CD, Freedman BI, Bowden DW.

Nephrol Dial Transplant. 2012 Apr;27(4):1505-11. doi: 10.1093/ndt/gfr522. Epub 2011 Oct 3.

PMID:
21968013
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

The association of the MYH9 gene and kidney outcomes in American Indians: the Strong Heart Family Study.

Franceschini N, Voruganti VS, Haack K, Almasy L, Laston S, Goring HH, Umans JG, Lee ET, Best LG, Fabsitz RR, MacCluer JW, Howard BV, North KE, Cole SA.

Hum Genet. 2010 Mar;127(3):295-301. doi: 10.1007/s00439-009-0769-8.

PMID:
19921264
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

HIV-associated nephropathy: experimental models.

Avila-Casado C, Fortoul TI, Chugh SS.

Contrib Nephrol. 2011;169:270-85. doi: 10.1159/000320212. Epub 2011 Jan 20.

PMID:
21252526
[PubMed - indexed for MEDLINE]

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