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  1. 1.   Disruption of MAGI2-RapGEF2-Rap1 signaling contributes to podocyte dysfunction in congenital nephrotic syndrome caused by mutations in MAGI2
  2. Zhu, Bingbing; Cao, Aili; Li, Jianhua; Young, James; Wong, Jenny; Ashraf, Shazia; Bierzynska, Agnieszka; Menon, Madhav C; Hou,Steven; Sawyers, Charles; Campbell, Kirk N; Saleem, Moin A; He, John C; Hildebrandt, Friedhelm; D'Agati, Vivette D; Peng, Wen; Kaufman, Lewis
  3. Kidney international. 2019, Sep; 96(3): 642-655.
  1. 2.   NPHS2 V260E Is a Frequent Cause of Steroid-Resistant Nephrotic Syndrome in Black South African Children
  2. Asharam, Kareshma; Bhimma, Rajendra; David,Victor; Coovadia, Hoosen M.; Qulu, Wenkosi P.; Naicker, Thajasvarie; Gillies, Christopher E.; Vega-Warner, Virginia; Johnson,Randy; Limou, Sophie; Kopp, Jeffrey B.; Sampson, Mathew; Nelson,George; Winkler,Cheryl
  3. KIDNEY INTERNATIONAL REPORTS. 2018, NOV; 3(6): 1354-1362.
  1. 3.   African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans
  2. Behar, D. M.; Rosset, S.; Tzur, S.; Selig, S.; Yudkovsky, G.; Bercovici, S.; Kopp, J. B.; Winkler, C. A.; Nelson, G. W.; Wasser, W. G.; Skorecki, K.
  3. Human Molecular Genetics. 2010, May; 19(9): 1816-1827.
  1. 4.   NPHS2 variation in sporadic focal segmental glomerulosclerosis
  2. McKenzie, L. M.; Hendrickson, S. L.; Briggs, W. A.; Dart, R. A.; Korbet, S. M.; Mokrzycki, M. H.; Kimmel, P. L.; Ahuja, T. S.; Berns, J. S.; Simon, E. E.; Smith, M. C.; Trachtman, H.; Michel, D. M.; Schelling, J. R.; Cho, M.; Zhou, Y. C.; Binns-Roemer, E.; Kirk, G. D.; Kopp, J. B.; Winkler, C. A.
  3. Journal of the American Society of Nephrology. 2007, Nov; 18(11): 2987-2995.
  1. 5.   NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: A HuGE review
  2. Franceschini, N.; North, K. E.; Kopp, J. B.; McKenzie, L.; Winkler, C.
  3. Genetics in Medicine. 2006, Feb; 8(2): 63-75.
  1. 6.   Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population
  2. Orloff, M. S.; Iyengar, S. K.; Winkler, C. A.; Goddard, K. A. B.; Dart, R. A.; Ahuja, T. S.; Mokrzycki, M.; Briggs, W. A.; Korbet, S. M.; Kimmel, P. L.; Simon, E. E.; Trachtman, H.; Vlahov, D.; Michel, D. M.; Berns, J. S.; Smith, M. C.; Schelling, J. R.; Sedor, J. R.; Kopp, J. B.
  3. Physiological Genomics. 2005, APR 14; 21(2): 212-221.
  1. 7.   CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility
  2. Kim, J. M.; Wu, H.; Green, G.; Winkler, C. A.; Kopp, J. B.; Miner, J. H.; Unanue, E. R.; Shaw, A. S.
  3. Science. 2003 300(5623): 1298-1300.
  1. 8.   Focal Segmental Glomerulosclerosis in Primates Infected With a Simian Immunodeficiency Virus
  2. Alpers, C. E.; Tsai, C. C.; Hudkins, K. L.; Cui, Y.; Kuller, L.; Benveniste, R. E.; Ward, J. M.; Morton, W. R.
  3. Aids Research and Human Retroviruses. 1997 13(5): 413-424.
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