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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2008 | 1 |
2009 | 1 |
2010 | 3 |
2024 | 0 |
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Page 1
MYH9 genetic variants associated with glomerular disease: what is the role for genetic testing?
Semin Nephrol. 2010 Jul;30(4):409-17. doi: 10.1016/j.semnephrol.2010.06.007.
Semin Nephrol. 2010.
PMID: 20807613
Free PMC article.
Association of trypanolytic ApoL1 variants with kidney disease in African Americans.
Genovese G, Friedman DJ, Ross MD, Lecordier L, Uzureau P, Freedman BI, Bowden DW, Langefeld CD, Oleksyk TK, Uscinski Knob AL, Bernhardy AJ, Hicks PJ, Nelson GW, Vanhollebeke B, Winkler CA, Kopp JB, Pays E, Pollak MR.
Genovese G, et al.
Science. 2010 Aug 13;329(5993):841-5. doi: 10.1126/science.1193032. Epub 2010 Jul 15.
Science. 2010.
PMID: 20647424
Free PMC article.
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Glomerular pathology in autosomal dominant MYH9 spectrum disorders: what are the clues telling us about disease mechanism?
Kopp JB.
Kopp JB.
Kidney Int. 2010 Jul;78(2):130-3. doi: 10.1038/ki.2010.82.
Kidney Int. 2010.
PMID: 20588287
Free PMC article.
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Advances in the biology and genetics of the podocytopathies: implications for diagnosis and therapy.
Barisoni L, Schnaper HW, Kopp JB.
Barisoni L, et al.
Arch Pathol Lab Med. 2009 Feb;133(2):201-16. doi: 10.5858/133.2.201.
Arch Pathol Lab Med. 2009.
PMID: 19195964
Free PMC article.
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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.
Kopp JB, et al.
Nat Genet. 2008 Oct;40(10):1175-84. doi: 10.1038/ng.226. Epub 2008 Sep 14.
Nat Genet. 2008.
PMID: 18794856
Free PMC article.
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