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Kidney International|March 14, 2018
Single-nephron proteomes connect morphology and function in proteinuric kidney diseaseMartin Höhne, Christian K Frese, Florian Grahammer, et al.
Nature Metabolism|July 23, 2020
A molecular mechanism explaining albuminuria in kidney diseaseLinus Butt, David Unnersjö-Jess, Martin Höhne, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 30, 2022
Definition, diagnosis and clinical management of non-obstructive kidney dysplasia: a consensus statement by the ERKNet Working Group on Kidney MalformationsStefan Kohl, Fred E Avni, Peter Boor, et al.
The EMBO Journal|August 23, 2012
AATF/Che-1 acts as a phosphorylation-dependent molecular modulator to repress p53-driven apoptosisKatja Höpker, Henning Hagmann, Safiya Khurshid, et al.
Cell Death & Disease|September 20, 2022
Primary cilia contribute to the aggressiveness of atypical teratoid/rhabdoid tumorsLena Blümel, Nan Qin, Johannes Berlandi, et al.
Kidney International|January 23, 2025
KDIGO 2025 clinical practice guideline for the evaluation, management, and treatment of autosomal dominant polycystic kidney disease (ADPKD): executive summaryVicente E Torres, Curie Ahn, Thijs R M Barten, et al.
Journal of the American Society of Nephrology : JASN|October 5, 2021
mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and CardiomyopathyKarl P Schlingmann, François Jouret, Kuang Shen, et al.
Kidney International Reports|August 19, 2024
Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 MicrodeletionsBénédicte Buffin-Meyer, Juliette Richard, Vincent Guigonis, et al.
Kidney International|March 23, 2025
Insights from ADPedKD, ERKReg and RaDaR registries provide a multi-national perspective on the presentation of childhood autosomal dominant polycystic kidney disease in high- and middle-income countriesCharlotte Gimpel, Steffen Fieuws, Jonas Hofstetter, et al.
Cell|August 7, 2012
Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signalingMoumita Chaki, Rannar Airik, Amiya K Ghosh, et al.
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