Gert Jan C. Veenstra

Professor

Radboud Universiteit Nijmegen Radboud Institute for Molecular Life Sciences

Netherlands

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Gert Jan C. Veenstra is a Professor at Radboud Universiteit Nijmegen, affiliated with the Radboud Institute for Molecular Life Sciences in the Netherlands. His research focuses on cellular differentiation, lineage commitment, and the role of gene regulatory networks in embryonic development. Recent articles explore advancements in cardiac differentiation, microcapsule technology for human embryoid bodies, and multi-omics studies related to enterocyte differentiation.

Articles (13)

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2025

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2023

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2023

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2022

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2022

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2022

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2022

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2021

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2021

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2021

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2021

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2020

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2020

Collaborators (5)

Georgios Georgiou

Head of Bioinformatics and Software Development

NETHERLANDS

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Robert Passier

Professor

Leiden University Medical Center

NETHERLANDS

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Jo Huiqing Zhou

Radboud University

NETHERLANDS

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Juan Zhang

Leiden University Medical Center

NETHERLANDS

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Michiel Vermeulen

Full professor

Radboud Universiteit Nijmegen

NETHERLANDS

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Gert Jan C. Veenstra

Research Interests

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Articles (13)

Cardiac differentiation roadmap for analysis of plasticity and balanced lineage commitment.

ONECUT2 regulates RANKL-dependent enterocyte and microfold cell differentiation in the small intestine; a multi-omics study

Mass production of lumenogenic human embryoid bodies and functional cardiospheres using in-air-generated microcapsules

The Role of Polycomb Proteins in Cell Lineage Commitment and Embryonic Development

Preparation of Intact Nuclei for Single-Nucleus Omics Using Frozen Cell Suspensions from Mutant Embryos of <i>Xenopus tropicalis</i>.

Uncovering the mesendoderm gene regulatory network through multi-omic data integration.

Conditional immortalization of human atrial myocytes for the generation of in vitro models of atrial fibrillation.

ANANSE: an enhancer network-based computational approach for predicting key transcription factors in cell fate determination

Isolation of multipotent progenitor cells from pleura and pericardium for tracheal tissue engineering purposes

Combinatorial transcription factor activities on open chromatin induce embryonic heterogeneity in vertebrates

Loss of PRC2 subunits primes lineage choice during exit of pluripotency

Two Functional Axes of Feedback-Enforced PRC2 Recruitment in Mouse Embryonic Stem Cells.

Genomics Methods for Xenopus Embryos and Tissues

Collaborators (5)

Georgios Georgiou

Robert Passier

Jo Huiqing Zhou

Juan Zhang

Michiel Vermeulen

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