Nathalie P. De Wagenaar

Rotterdam, ZH, Netherlands

Last Updated: 09/26/2026

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Found 9 publications

Restrictor slows RNAPII elongation to promote termination at noncoding RNA loci.

Restrictor slows RNAPII elongation to promote termination at noncoding RNA loci.

Journal: Genes & development
Published: January 21, 2025

Restrictor slows early transcription elongation to render RNA polymerase II susceptible to termination at non-coding RNA loci.

Restrictor slows early transcription elongation to render RNA polymerase II susceptible to termination at non-coding RNA loci.

Journal: bioRxiv : the preprint server for biology
Published: January 20, 2025

Functional analysis of cell lines derived from SMAD3-related Loeys-Dietz syndrome patients provides insights into genotype-phenotype relation.

Functional analysis of cell lines derived from SMAD3-related Loeys-Dietz syndrome patients provides insights into genotype-phenotype relation.

Journal: Human molecular genetics
Published: February 01, 2024

Dissecting the roles of MBD2 isoforms and domains in regulating NuRD complex function during cellular differentiation.

Dissecting the roles of MBD2 isoforms and domains in regulating NuRD complex function during cellular differentiation.

Journal: Nature communications
Published: April 20, 2022

Contraction pressure analysis using optical imaging in normal and MYBPC3-mutated hiPSC-derived cardiomyocytes grown on matrices with tunable stiffness.

Contraction pressure analysis using optical imaging in normal and MYBPC3-mutated hiPSC-derived cardiomyocytes grown on matrices with tunable stiffness.

Journal: Biomaterials and biosystems
Published: April 08, 2022

DNA sequence and chromatin modifiers cooperate to confer epigenetic bistability at imprinting control regions.

DNA sequence and chromatin modifiers cooperate to confer epigenetic bistability at imprinting control regions.

Journal: Nature genetics
Published: June 10, 2021

Molecular phenotyping and functional assessment of smooth muscle-like cells with pathogenic variants in aneurysm genes ACTA2, MYH11, SMAD3 and FBN1.

Molecular phenotyping and functional assessment of smooth muscle-like cells with pathogenic variants in aneurysm genes ACTA2, MYH11, SMAD3 and FBN1.

Journal: Human molecular genetics
Published: May 05, 2021

Transforming Growth Factor-β and the Renin-Angiotensin System in Syndromic Thoracic Aortic Aneurysms: Implications for Treatment.

Transforming Growth Factor-β and the Renin-Angiotensin System in Syndromic Thoracic Aortic Aneurysms: Implications for Treatment.

Journal: Cardiovascular drugs and therapy
Published: November 18, 2020

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
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Last Updated: 09/26/2026