Krappitz Lab

Lab Overview

Thurman LabThe Krappitz Lab investigates the molecular mechanisms underlying autosomal-dominant polycystic kidney disease (ADPKD), with a focus on therapeutic approaches informed by the group’s published work. The lab has contributed to establishing both chaperone-based strategies and gene-editing approaches in PKD, demonstrating how proteostasis correction and base editing can stabilize polycystin function and improve cystic outcomes in experimental models. Current efforts continue to integrate mechanistic discovery with translational development to advance targeted therapies for PKD.

Publications

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Valosin-containing protein in ciliary morphology: a novel target in ADPKD

Carlotta Pioppini, Rishi Bhardwaj, Ria Schönauer, Jan Halbritter, Fatima Hassan, Kai-Uwe Eckardt, Sorin V Fedeles, Duygu Elif Yilmaz, Matteus Krappitz
PMID: 40662578 DOI: 10.1152/ajprenal.00032.2025


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Detection of pro angiogenic and inflammatory biomarkers in patients with CKD.

Matteus Krappitz, Rishi Bhardwaj, Ke Dong, Tobias Staudner, Duygu Elif Yilmaz 2, Carlotta Pioppini 2, Parisa Westergerling, David Ruemmele, Till Hollmann, Thuy Anh Nguyen, Yiqiang Cai, Anna-Rachel Gallagher, Stefan Somlo, Sorin Fedeles 
PMID: 36270750 PMCID: PMC10101557 DOI: 10.1681/ASN.2021091180
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In vivo base editing reduces liver cysts in autosomal dominant polycystic kidney disease

Antonia Ibel, Rishi Bhardwaj, Duygu Elif Yilmaz, Shuhan Kong, Sarah Wendlinger, Dimitra Papaioannou, Claudia Diezemann, Kai-Uwe Eckardt, Fatima Hasan, Verena Klämbt, Jan Halbritter, Sorin Fedeles, Matteus Krappitz, Michael M Kaminski
PMID: 39975003 PMCID: PMC11839015 DOI: 10.1101/2025.02.07.636600

Personnel

Dr. Krappitz Headshot

Matteus Krappitz, MD

Ashish Gorule

Ashish Gorule, PhD


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