Defining cellular and molecular identities within the kidney is necessary to understand its organization and function in health and disease. Here we demonstrate a reproducible method with minimal arti
Mis-sense mutations of Inverted Formin 2 (INF2) are among the most common causes of genetic FSGS with or without Charcot-Marie-Tooth (CMT) disease. Here, we extracted glomeruli from Heterozygous INF2
Background: Chemokines are a family of proteins mainly mediating the homing and migration of various cells. The CXC chemokine CXCL12 is a member of low-weight-molecular chemokines. In the kidney, CXCL
To analyze gene expression differences between WT proximal tubule cells and cells in which, by siRNA transfection, we blunted the expression of GLUT2 gene to mimic Fanconi Bickel Syndrome Total RNA wa
ALT - alanine aminotransferase, genotypes of IL28B: CC and not CC (CT and TT). In liverbiopsy: G- grade of inflammation and necrosis, S-stage of fibrosis.*Genotype 1 versus 3 p = 0.0501, genotype 1 ve