Tobias Hermle
Universitätsklinikum Freiburg
28 papers found
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Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Download from www.nature.comMutations in multiple components of the nuclear pore complex cause nephrotic syndrome
Download from doi.orgMutations in WDR4 as a new cause of Galloway-Mowat syndrome
UploadGAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic Syndrome
UploadMutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment
Download from doi.orgPanel sequencing distinguishes monogenic forms of nephritis from nephrosis in children
UploadGenetic variants in the LAMA5 gene in pediatric nephrotic syndrome
UploadUsing the Drosophila Nephrocyte to Model Podocyte Function and Disease
Download from doi.orgWhole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome
UploadMutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
Download from www.nature.comMutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome
Download from www.nature.comRegulation of Frizzled-Dependent Planar Polarity Signaling by a V-ATPase Subunit
Download from doi.orgMissing publications? Search for publications with a matching author name.