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Page 1
A new locus for familial FSGS on chromosome 2p.
Gbadegesin R, Lavin P, Janssens L, Bartkowiak B, Homstad A, Wu G, Bowling B, Eckel J, Potocky C, Abbott D, Conlon P, Scott WK, Howell D, Hauser E, Winn MP. Gbadegesin R, et al. Among authors: winn mp. J Am Soc Nephrol. 2010 Aug;21(8):1390-7. doi: 10.1681/ASN.2009101046. Epub 2010 Jul 8. J Am Soc Nephrol. 2010. PMID: 20616172 Free PMC article.
TRPC6 enhances angiotensin II-induced albuminuria.
Eckel J, Lavin PJ, Finch EA, Mukerji N, Burch J, Gbadegesin R, Wu G, Bowling B, Byrd A, Hall G, Sparks M, Zhang ZS, Homstad A, Barisoni L, Birbaumer L, Rosenberg P, Winn MP. Eckel J, et al. Among authors: winn mp. J Am Soc Nephrol. 2011 Mar;22(3):526-35. doi: 10.1681/ASN.2010050522. Epub 2011 Jan 21. J Am Soc Nephrol. 2011. PMID: 21258036 Free PMC article.
TNXB mutations can cause vesicoureteral reflux.
Gbadegesin RA, Brophy PD, Adeyemo A, Hall G, Gupta IR, Hains D, Bartkowiak B, Rabinovich CE, Chandrasekharappa S, Homstad A, Westreich K, Wu G, Liu Y, Holanda D, Clarke J, Lavin P, Selim A, Miller S, Wiener JS, Ross SS, Foreman J, Rotimi C, Winn MP. Gbadegesin RA, et al. Among authors: winn mp. J Am Soc Nephrol. 2013 Jul;24(8):1313-22. doi: 10.1681/ASN.2012121148. Epub 2013 Apr 25. J Am Soc Nephrol. 2013. PMID: 23620400 Free PMC article.
Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS.
Gbadegesin RA, Hall G, Adeyemo A, Hanke N, Tossidou I, Burchette J, Wu G, Homstad A, Sparks MA, Gomez J, Jiang R, Alonso A, Lavin P, Conlon P, Korstanje R, Stander MC, Shamsan G, Barua M, Spurney R, Singhal PC, Kopp JB, Haller H, Howell D, Pollak MR, Shaw AS, Schiffer M, Winn MP. Gbadegesin RA, et al. Among authors: winn mp. J Am Soc Nephrol. 2014 Sep;25(9):1991-2002. doi: 10.1681/ASN.2013090976. Epub 2014 Mar 27. J Am Soc Nephrol. 2014. PMID: 24676636 Free PMC article.
A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.
Hall G, Gbadegesin RA, Lavin P, Wu G, Liu Y, Oh EC, Wang L, Spurney RF, Eckel J, Lindsey T, Homstad A, Malone AF, Phelan PJ, Shaw A, Howell DN, Conlon PJ, Katsanis N, Winn MP. Hall G, et al. Among authors: winn mp. J Am Soc Nephrol. 2015 Apr;26(4):831-43. doi: 10.1681/ASN.2013101053. Epub 2014 Aug 21. J Am Soc Nephrol. 2015. PMID: 25145932 Free PMC article.
TORCing up the importance of calcium signaling.
Lavin PJ, Winn MP. Lavin PJ, et al. Among authors: winn mp. J Am Soc Nephrol. 2011 Aug;22(8):1391-3. doi: 10.1681/ASN.2011060595. Epub 2011 Jul 14. J Am Soc Nephrol. 2011. PMID: 21757772 No abstract available.
Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis.
Gbadegesin RA, Lavin PJ, Hall G, Bartkowiak B, Homstad A, Jiang R, Wu G, Byrd A, Lynn K, Wolfish N, Ottati C, Stevens P, Howell D, Conlon P, Winn MP. Gbadegesin RA, et al. Among authors: winn mp. Kidney Int. 2012 Jan;81(1):94-9. doi: 10.1038/ki.2011.297. Epub 2011 Aug 24. Kidney Int. 2012. PMID: 21866090 Free PMC article.
43 results