Sylvia C. Van Beersum
Nijmegen, GE, Netherlands
Last Updated: 09/26/2026
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Found 16 publications
A targeted multi-proteomics approach generates a blueprint of the ciliary ubiquitinome.
Journal: Frontiers in cell and developmental biology
Published: December 01, 2022
PDE6D Mediates Trafficking of Prenylated Proteins NIM1K and UBL3 to Primary Cilia.
Journal: Cells
Published: October 14, 2022
PCARE and WASF3 regulate ciliary F-actin assembly that is required for the initiation of photoreceptor outer segment disk formation.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 22, 2020
CiliaCarta: An integrated and validated compendium of ciliary genes.
Journal: PloS one
Published: October 17, 2018
Recurrent De Novo Mutations Disturbing the GTP/GDP Binding Pocket of RAB11B Cause Intellectual Disability and a Distinctive Brain Phenotype.
Journal: American journal of human genetics
Published: June 14, 2017
Missense mutations in the WD40 domain of AHI1 cause non-syndromic retinitis pigmentosa.
Journal: Journal of medical genetics
Published: July 29, 2016
Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.
Journal: Nature communications
Published: March 30, 2016
An organelle-specific protein landscape identifies novel diseases and molecular mechanisms.
Journal: Nature communications
Published: February 15, 2016
KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome.
Journal: Genome biology
Published: July 06, 2015
The Interaction of CCDC104/BARTL1 with Arl3 and Implications for Ciliary Function.
Journal: Structure (London, England : 1993)
Published: June 09, 2015
Last Updated: 09/26/2026