Daniel Epting
Freiburg, BW, Germany
Last Updated: 09/26/2026
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Found 22 publications
BICC1 interacts with PKD1 and PKD2 to drive cystogenesis in ADPKD.
Journal: eLife
Published: February 12, 2026
Correction: Tulp3 deficiency results in ciliopathy phenotypes during zebrafish embryogenesis.
Journal: Scientific reports
Published: January 12, 2026
PATJ deficiency leads to cystic kidney disease and related ciliopathies.
Journal: HGG advances
Published: April 22, 2025
Tulp3 deficiency results in ciliopathy phenotypes during zebrafish embryogenesis.
Journal: Scientific reports
Published: February 03, 2025
Author Correction: Microridge-like structures anchor motile cilia.
Journal: Nature communications
Published: September 23, 2024
BICC1 Interacts with PKD1 and PKD2 to Drive Cystogenesis in ADPKD.
Journal: bioRxiv : the preprint server for biology
Published: September 10, 2024
Kif21a deficiency leads to impaired glomerular filtration barrier function.
Journal: Scientific reports
Published: July 26, 2023
PATJ inhibits histone deacetylase 7 to control tight junction formation and cell polarity.
Journal: Cellular and molecular life sciences : CMLS
Published: June 06, 2023
A novel role for the chloride intracellular channel protein Clic5 in ciliary function.
Journal: Scientific reports
Published: December 05, 2022
Progressive liver, kidney, and heart degeneration in children and adults affected by TULP3 mutations.
Journal: American journal of human genetics
Published: December 23, 2021
The ciliary transition zone protein TMEM218 synergistically interacts with the NPHP module and its reduced dosage leads to a wide range of syndromic ciliopathies.
Journal: Human molecular genetics
Published: November 17, 2021
Ift88, but not Kif3a, is required for establishment of the periciliary membrane compartment.
Journal: Biochemical and biophysical research communications
Published: September 17, 2021
Last Updated: 09/26/2026