[HTML][HTML] Podocyte injury and its consequences
M Nagata - Kidney international, 2016 - Elsevier
Podocytes maintain the glomerular filtration barrier, and the stability of this barrier depends
on their highly differentiated postmitotic phenotype, which also defines the particular …
on their highly differentiated postmitotic phenotype, which also defines the particular …
Alport syndrome—insights from basic and clinical research
J Kruegel, D Rubel, O Gross - Nature Reviews Nephrology, 2013 - nature.com
Abstract In 1927, Arthur C. Alport first published his description of a triad of symptoms in a
family with hereditary congenital haemorrhagic nephritis, deafness and ocular changes. A …
family with hereditary congenital haemorrhagic nephritis, deafness and ocular changes. A …
Hereditary proteinuria syndromes and mechanisms of proteinuria
K Tryggvason, J Patrakka… - New England Journal of …, 2006 - Mass Medical Soc
Hereditary Proteinuria Syndromes and Mechanisms of Proteinuria | New England Journal of
Medicine Skip to main content The New England Journal of Medicine homepage Advanced …
Medicine Skip to main content The New England Journal of Medicine homepage Advanced …
Nck adaptor proteins link nephrin to the actin cytoskeleton of kidney podocytes
N Jones, IM Blasutig, V Eremina, JM Ruston, F Bladt… - Nature, 2006 - nature.com
The glomerular filtration barrier in the kidney is formed in part by a specialized intercellular
junction known as the slit diaphragm, which connects adjacent actin-based foot processes of …
junction known as the slit diaphragm, which connects adjacent actin-based foot processes of …
Defining cell-type specificity at the transcriptional level in human disease
W Ju, CS Greene, F Eichinger, V Nair… - Genome …, 2013 - genome.cshlp.org
Cell-lineage–specific transcripts are essential for differentiated tissue function, implicated in
hereditary organ failure, and mediate acquired chronic diseases. However, experimental …
hereditary organ failure, and mediate acquired chronic diseases. However, experimental …
[HTML][HTML] Podocytes in culture: past, present, and future
SJ Shankland, JW Pippin, J Reiser, P Mundel - Kidney international, 2007 - Elsevier
Human genetic and in vivo studies have helped to define the critical importance of
podocytes for kidney function in health and disease. However, as in any other research …
podocytes for kidney function in health and disease. However, as in any other research …
Epithelial-to-mesenchymal transition is a potential pathway leading to podocyte dysfunction and proteinuria
Y Li, YS Kang, C Dai, LP Kiss, X Wen, Y Liu - The American journal of …, 2008 - Elsevier
Podocyte dysfunction plays an essential role in the pathogenesis of proteinuria and
glomerulosclerosis. However, the mechanism underlying podocyte dysfunction in many …
glomerulosclerosis. However, the mechanism underlying podocyte dysfunction in many …
[HTML][HTML] NPHS2 mutation analysis shows genetic heterogeneityof steroid-resistant nephrotic syndrome and lowpost-transplant recurrence
S Weber, O Gribouval, EL Esquivel, V Morinière… - Kidney international, 2004 - Elsevier
NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic
syndrome and low post-transplant recurrence. Background Mutations of NPHS2 are …
syndrome and low post-transplant recurrence. Background Mutations of NPHS2 are …
Nephrin signaling in the podocyte: an updated view of signal regulation at the slit diaphragm and beyond
Podocytes are a major component of the glomerular blood filtration barrier, and alterations to
the morphology of their unique actin-based foot processes (FP) are a common feature of …
the morphology of their unique actin-based foot processes (FP) are a common feature of …