André Pawlak

Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders

Herma Portsteffen, Andreas Beyer, E. Becker et al. · Nature Genetics · 1997 · 151 citations

Complementation Group 1, Peroxisome Biogenesis Disorders, Mendelian Disorder +10

A Novel Approach to Investigation of the Pathogenesis of Active Minimal-Change Nephrotic Syndrome Using Subtracted cDNA Library Screening

Djillali Sahali, André Pawlak, Asta Valančiūtė et al. · Journal of the American Society of Nephrology · 2002 · 110 citations · Full text

c-mip Impairs Podocyte Proximal Signaling and Induces Heavy Proteinuria

Shaoyu Zhang, Maud Kamal, Karine Dahan et al. · Science Signaling · 2010 · 104 citations · Full text

Expression patterns of RelA and c-mip are associated with different glomerular diseases following anti-VEGF therapy

Hassan Izzedine, M. Mangier, Virginie Ory et al. · Kidney International · 2013 · 100 citations · Full text

NEPHRUTIX: A randomized, double-blind, placebo vs Rituximab-controlled trial assessing T-cell subset changes in Minimal Change Nephrotic Syndrome

A. Boumédiène, Pauline Vachin, Kélhia Sendeyo et al. · Journal of Autoimmunity · 2017 · 92 citations

Glomerulonephritis, Rituximab-controlled Trial, T-cell Subset Changes +5