Dorus A. Mans

Nijmegen, GE, Netherlands

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 16 publications

CiliaCarta: An integrated and validated compendium of ciliary genes.

CiliaCarta: An integrated and validated compendium of ciliary genes.

Journal: PloS one
Published: October 17, 2018

Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility.

Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility.

Journal: PLoS genetics
Published: March 23, 2018

Liver cyst gene knockout in cholangiocytes inhibits cilium formation and Wnt signaling.

Liver cyst gene knockout in cholangiocytes inhibits cilium formation and Wnt signaling.

Journal: Human molecular genetics
Published: May 24, 2017

Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.

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.

An organelle-specific protein landscape identifies novel diseases and molecular mechanisms.

Journal: Nature communications
Published: February 15, 2016

A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome.

A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome.

Journal: Cilia
Published: September 03, 2015

The Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle Trafficking.

The Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle Trafficking.

Journal: PLoS genetics
Published: February 26, 2015

Medical genetics of ciliopathies.

Medical genetics of ciliopathies.

Journal: Journal of pediatric genetics
Published: December 23, 2014

TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.

TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.

Journal: Nature communications
Published: October 01, 2014

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes.

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes.

Journal: Nature cell biology
Published: July 17, 2014

CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation.

CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation.

Journal: American journal of human genetics
Published: May 23, 2014

Elution profile analysis of SDS-induced subcomplexes by quantitative mass spectrometry.

Elution profile analysis of SDS-induced subcomplexes by quantitative mass spectrometry.

Journal: Molecular & cellular proteomics : MCP
Published: February 25, 2014
Showing 1-12 of 16

Last Updated: 09/26/2026