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Abstract

Although the molecular mechanisms underlying the pathophysiology of minimal change nephrotic syndrome (MCNS) remain unclear, clinical and experimental observations point to an immune origin. MCNS is currently considered as being caused by a putative circulating factor which increases glomerular permeability and leads to podocyte cytoskeleton disorganization and proteinuria. We recently identified c-mip (c-maf-inducing protein) as a key factor involved in lymphocyte and podocyte dysfunction observed in MCNS patients. The aim of this review is to describe recent findings about the potential role of c-mip into MCNS pathogenesis.

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Audard, V., Pawlak, A., Sahali, D. (2016). The Role of c-mip in the Pathogenesis of Minimal Change Nephrotic Syndrome. In: Kaneko, K. (eds) Molecular Mechanisms in the Pathogenesis of Idiopathic Nephrotic Syndrome. Springer, Tokyo. https://doi.org/10.1007/978-4-431-55270-3_6

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  • DOI: https://doi.org/10.1007/978-4-431-55270-3_6

  • Publisher Name: Springer, Tokyo

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  • Online ISBN: 978-4-431-55270-3

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