Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Violetta Antal-Kónya"'
Autor:
Dániel Seidl, Violetta Antal-Kónya, Gusztáv Schay, Aurélia Bertholet-Thomas, György Török, Geraldine Mollet, Miklós Kellermayer, Corinne Antignac, Kálmán Tory
Publikováno v:
Nephrology Dialysis Transplantation. 37
BACKGROUND AND AIMS Mutations of NPHS2 cause autosomal recessive steroid-resistant nephrotic syndrome (SRNS). The encoded podocin, a key component of the slit diaphragm, homo-oligomerizes through two C-terminal oligomerization sites. We formerly foun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::148db9f4c91626f4e7cd925884c403aa
https://doi.org/10.1093/ndt/gfac062.025
https://doi.org/10.1093/ndt/gfac062.025
Autor:
Violetta Antal-Kónya, Domonkos Pap, Gusztáv Schay, Máté Kétszeri, Anita Ungvári-Veres, Tivadar Tulassay, Miklós Kellermayer, Dóra Karancsiné Menyhárd, Kálmán Tory
Publikováno v:
Nephrology Dialysis Transplantation. 37
BACKGROUND AND AIMS The podocin encoding NPHS2 is the most frequently mutated gene in steroid-resistant nephrotic syndrome. Podocin homooligomerizes through C-terminal helical regions [1] and binds nephrin in the glomerular slit diaphragm [2]. We for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d811aa7670bc70c7b5b4a6384015677
https://doi.org/10.1093/ndt/gfac097.002
https://doi.org/10.1093/ndt/gfac097.002