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Biorxiv : the Preprint Server for Biology|July 16, 2025
Loss of Bbs8 leads to cystic kidney disease in mice with reduced acetylation of ciliary alpha-tubulin through HDAC2Emilia Kieckhöfer, Julia Günzler, Peter A Matthiessen, et al.
Kidney Medicine|November 10, 2025
Qualitative Analysis and Comparison of Externally Led Patient-Focused Drug Development Concepts for Autosomal Recessive Polycystic Kidney Disease Against SONG InitiativesBelle Soyfer, Sorin Fedeles, Wendy Ruyle, et al.
Journal of Cellular and Molecular Medicine|October 28, 2020
The carboxy-terminus of the human ARPKD protein fibrocystin can control STAT3 signalling by regulating SRC-activationClaudia Dafinger, Amrei M Mandel, Alina Braun, et al.
Kidney International Reports|September 14, 2019
ADPedKD: A Global Online Platform on the Management of Children With ADPKDStéphanie De Rechter, Detlef Bockenhauer, Lisa M Guay-Woodford, et al.
Plos One|May 22, 2013
Dysregulated autophagy contributes to podocyte damage in Fabry's diseaseMax C Liebau, Fabian Braun, Katja Höpker, et al.
Clinical Kidney Journal|May 5, 2025
Urinary peptide signature distinguishes autosomal recessive polycystic kidney disease from other causes of chronic kidney diseaseKathrin Burgmaier, Bénédicte Buffin-Meyer, Julie Klein, et al.
Neuropediatrics|August 31, 2018
Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech DevelopmentWalid Fazeli, Kerstin Becker, Peter Herkenrath, et al.
Pediatric Nephrology (Berlin, Germany)|November 28, 2017
Mycophenolate mofetil following glucocorticoid treatment in Henoch-Schönlein purpura nephritis: the role of early initiation and therapeutic drug monitoringAgnes Hackl, Jan U Becker, Lisa M Körner, et al.
Archives of Gynecology and Obstetrics|January 5, 2023
Single-center outcome analysis of 46 fetuses with megacystis after intrauterine vesico-amniotic shunting with the Somatex®intrauterine shuntI Gottschalk, C Berg, T Menzel, et al.
Journal of Molecular Medicine (Berlin, Germany)|January 25, 2013
Conditional loss of kidney microRNAs results in congenital anomalies of the kidney and urinary tract (CAKUT)Malte P Bartram, Martin Höhne, Claudia Dafinger, et al.
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