Stefanie Kuhns

Dublin, L, Ireland

Last Updated: 09/26/2026

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Found 10 publications

Intraflagellar transport protein IFT172 contains a C-terminal ubiquitin-binding U-box-like domain involved in ciliary signaling.

Intraflagellar transport protein IFT172 contains a C-terminal ubiquitin-binding U-box-like domain involved in ciliary signaling.

Journal: eLife
Published: June 23, 2026

Endogenous Tagging of Ciliary Genes in Human RPE1 Cells for Live-Cell Imaging.

Endogenous Tagging of Ciliary Genes in Human RPE1 Cells for Live-Cell Imaging.

Journal: Methods in molecular biology (Clifton, N.J.)
Published: October 19, 2023

Transient accumulation and bidirectional movement of KIF13B in primary cilia.

Transient accumulation and bidirectional movement of KIF13B in primary cilia.

Journal: Journal of cell science
Published: August 11, 2021

ERICH3 in Primary Cilia Regulates Cilium Formation and the Localisations of Ciliary Transport and Sonic Hedgehog Signaling Proteins.

ERICH3 in Primary Cilia Regulates Cilium Formation and the Localisations of Ciliary Transport and Sonic Hedgehog Signaling Proteins.

Journal: Scientific reports
Published: May 13, 2019

Rab35 controls cilium length, function and membrane composition.

Rab35 controls cilium length, function and membrane composition.

Journal: EMBO reports
Published: December 19, 2018

Rab GTPases in cilium formation and function.

Rab GTPases in cilium formation and function.

Journal: Small GTPases
Published: October 27, 2017

Primary Cilium Formation and Ciliary Protein Trafficking Is Regulated by the Atypical MAP Kinase MAPK15 in Caenorhabditis elegans and Human Cells.

Primary Cilium Formation and Ciliary Protein Trafficking Is Regulated by the Atypical MAP Kinase MAPK15 in Caenorhabditis elegans and Human Cells.

Journal: Genetics
Published: June 05, 2017

Cilia Train Spotting.

Cilia Train Spotting.

Journal: Developmental cell
Published: June 09, 2016

TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome.

TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome.

Journal: Nature cell biology
Published: August 11, 2015

KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome.

KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome.

Journal: Genome biology
Published: July 06, 2015
Showing 1-10 of 10

Last Updated: 09/26/2026