Molecular Mechanisms in the Pathogenesis of Idiopathic Nephrotic Syndrome (Paperback, Softcover reprint of the original 1st ed. 2016)

This comprehensive book reviews our current state of knowledge about the pathogenesis of idiopathic nephrotic syndrome (INS), which comprises a heterogeneous group of diseases with distinct histological characteristics, such as minimal-change nephrotic syndrome (MCNS), focal segmental glomerulosclerosis (FSGS), and idiopathic membranous nephropathy (IMN). As the word "idiopathic" indicates, the pathogenesis of INS remains unclear. Historically, T-cell dysfunction has been thought to play an important part in the pathogenesis of MCNS, while circulating vascular permeabilities have been believed to induce proteinuria in FSGS. The book further describes recent advances in molecular biology, which have allowed us to speculate on the interactions between visceral glomerular epithelial cells (podocytes) and the relative significance of several molecules in the pathogenesis of INS, such as reactive oxygen species, nuclear factor-kappa B, CD80, angiopoietin-like 4, cardiotrophin-like cytokine-1, and M-type phospholipase A2 receptor. The normally rapid pace of scientific progress occasionally devolves into a state of chaos, and the pathogenetic research on INS is one such case. This volume will help researchers and scientists to collaborate, share resources, and expedite the design of protocols to evaluate the putative factors.

General

Imprint:	Springer Verlag,Japan
Country of origin:	Japan
Release date:	August 2016
First published:	2016
Editors:	Kazunari Kaneko
Dimensions:	235 x 155mm (L x W)
Format:	Paperback
Pages:	240
Edition:	Softcover reprint of the original 1st ed. 2016
ISBN-13:	978-4-431-56279-5
Categories:	Books > Medicine > Clinical & internal medicine > Urology & urogenital medicine Books > Medicine > General issues > Medical equipment & techniques > Medical research Books > Medicine > Clinical & internal medicine > Renal medicine > General Promotions
LSN:	4-431-56279-6
Barcode:	9784431562795

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