Kai Fenzl

7PUBLICATIONS
69CO-AUTHORS
Respiratory diseasesGene and molecular therapyPolymerisation mechanismsCardiology (incl. cardiovascular diseases)Neurology and neuromuscular diseases
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Publications (7)

|Jul 29, 2026
Damaging RBM20 E-rich domain variants are not rescued by gene replacement.

|Sep 08, 2025
AAV9-Mediated TNPO3 Overexpression in the Heart Rescues RBM20 Cardiomyopathy in Mice.

Julia Kornienko, Laura Schraft, Kai Fenzl

|Aug 15, 2025
Co-translational ribosome pairing enables native assembly of misfolding-prone subunits.

Florian Wruck, Jaro Schmitt, Katharina Till

|Aug 08, 2025
The contribution of RBM20 truncating variants to human cardiomyopathy.

Brendan J Floyd, Joyce N Njoroge, Vikki A Krysov

|Jul 18, 2023
Mislocalization of pathogenic RBM20 variants in dilated cardiomyopathy is caused by loss-of-interaction with Transportin-3.

Julia Kornienko, Marta Rodríguez-Martínez, Kai Fenzl

|Jan 01, 2021
Interactions between nascent proteins translated by adjacent ribosomes drive homomer assembly.

Matilde Bertolini, Kai Fenzl, Ilia Kats

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Frequent Collaborators

3 joint publications

Lars Steinmetz

3 joint publications

Günter Kramer

3 joint publications

Benjamin Meder

2 joint publications

Matilde Bertolini