Genetics of Familial FSGS
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference17 articles.
1. A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13;Mathis;Kidney Int,1998
2. Alpha-actinin-4 is required for normal podocyte adhesion;Dandapani;J Biol Chem,2007
3. Mice with altered alpha-actinin-4 expression have distinct morphologic patterns of glomerular disease;Henderson;Kidney Int,2008
4. Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis;Kaplan;Nat Genet,2000
5. Mutational and biological analysis of alpha-actinin-4 in focal segmental glomerulosclerosis;Weins;J Am Soc Nephrol,2005
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1. Role of formin INF2 in human diseases;Molecular Biology Reports;2021-10-26
2. Spontaneous remission of genetic, apparent primary, FSGS presenting with nephrotic syndrome challenges traditional notions of primary FSGS;Journal of Nephrology;2020-08-27
3. A Deregulated Stress Response Underlies Distinct INF2-Associated Disease Profiles;Journal of the American Society of Nephrology;2020-05-22
4. FSGS-Causing INF2 Mutation Impairs Cleaved INF2 N-Fragment Functions in Podocytes;Journal of the American Society of Nephrology;2020-01-10
5. A deregulated stress response underlies distinct INF2 associated disease profiles;2019-11-12
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