Elisabeth Ott

Freiburg, BW, Germany

Last Updated: 09/26/2026

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Found 12 publications

BICC1 interacts with PKD1 and PKD2 to drive cystogenesis in ADPKD.

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.

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.

PATJ deficiency leads to cystic kidney disease and related ciliopathies.

Journal: HGG advances
Published: April 22, 2025

Genetic screens of imaging-derived kidney volumes identify genes linked to kidney function.

Genetic screens of imaging-derived kidney volumes identify genes linked to kidney function.

Journal: Kidney international
Published: March 26, 2025

Tulp3 deficiency results in ciliopathy phenotypes during zebrafish embryogenesis.

Tulp3 deficiency results in ciliopathy phenotypes during zebrafish embryogenesis.

Journal: Scientific reports
Published: February 03, 2025

BICC1 Interacts with PKD1 and PKD2 to Drive Cystogenesis in ADPKD.

BICC1 Interacts with PKD1 and PKD2 to Drive Cystogenesis in ADPKD.

Journal: bioRxiv : the preprint server for biology
Published: September 10, 2024

A novel role for the chloride intracellular channel protein Clic5 in ciliary function.

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.

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.

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

Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome.

Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome.

Journal: Human mutation
Published: June 20, 2019

Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease.

Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease.

Journal: Nature genetics
Published: June 06, 2016

Pronephric tubule morphogenesis in zebrafish depends on Mnx mediated repression of irx1b within the intermediate mesoderm.

Pronephric tubule morphogenesis in zebrafish depends on Mnx mediated repression of irx1b within the intermediate mesoderm.

Journal: Developmental biology
Published: May 11, 2015
Showing 1-12 of 12

Last Updated: 09/26/2026