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An unexpected role of steroid on podocytes: from zebrafish to human nephrotic syndrome?
Author(s) -
Catherine Meyer-Schwesinger
Publication year - 2019
Publication title -
kidney international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.499
H-Index - 276
eISSN - 1523-1755
pISSN - 0085-2538
DOI - 10.1016/j.kint.2019.01.044
Subject(s) - nephrotic syndrome , zebrafish , context (archaeology) , proteinuria , medicine , kidney , endocrinology , cancer research , biology , genetics , gene , paleontology
In this issue of Kidney International, Jobst-Schwan et al. developed a zebrafish model of MAGI2-deficiency, which recapitulates findings of human nephrotic syndrome due to MAGI2 mutations. The authors use this model system to screen for drugs that might target and alleviate MAGI2-associated nephrotic syndrome pathways. The scientific context of this publication and the significance of its key findings are discussed in this commentary.

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