Marius Regin

Vrije Universiteit Brussel

Belgium

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Articles (17)

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2025

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2025

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2025

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2024

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2024

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2024

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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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2021

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2021

Collaborators (18)

Anfien Huyghebaert

Vrije Universiteit Brussel

BELGIUM

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Kathy Niakan

The Francis Crick Institute

UNITED KINGDOM

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Panagiotis Stamatiadis

Vrije Universiteit Brussel

BELGIUM

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Nusa Krivec

Vrije Universiteit Brussel

BELGIUM

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Hilde Van De Velde

Vrije Universiteit Brussel

BELGIUM

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Katrien Stouffs

Vrije Universiteit Brussel

BELGIUM

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Claire Simon

University of Cambridge

UNITED KINGDOM

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Greta Verheyen

Head ART laboratory

BELGIUM

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Mary-Louise Bonduelle

Vrije Universiteit Brussel

BELGIUM

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Diana AlDelbany

Université libre de Bruxelles (ULB)

BELGIUM

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Karen Sermon

Vrije Universiteit Brussel

BELGIUM

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Florence Belva

Vrije Universiteit Brussel

BELGIUM

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Pieter Verdyck

Vrije Universiteit Brussel

BELGIUM

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Stefaan Verhulst

Karolinska Institutet

SWEDEN

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Alexander Gheldof

Vrije Universiteit Brussel

BELGIUM

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willem verpoest

Professor

Vrije Universiteit Brussel

BELGIUM

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Sara Seneca

Vrije Universiteit Brussel

BELGIUM

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Claudia Spits

Vrije Universiteit Brussel

BELGIUM

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Marius Regin

Research Interests

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Articles (17)

Atypical Chemokine Receptor CCRL2 Shapes Tumor Spheroid Structure and Immune Signaling in Melanoma

Loss of 18q Alters TGFβ Signalling Affecting Anteroposterior Neuroectodermal Fate in Human Embryonic Stem Cells

The interplay between mitochondrial DNA genotypes, female infertility, ovarian response, and mutagenesis in oocytes

Children born after assisted reproduction more commonly carry a mitochondrial genotype associating with low birthweight

SALL3 mediates the loss of neuroectodermal differentiation potential in human embryonic stem cells with chromosome 18q loss

De Novo Cancer Mutations Frequently Associate with Recurrent Chromosomal Abnormalities during Long-Term Human Pluripotent Stem Cell Culture

Prenatal treprostinil improves pulmonary arteriolar hypermuscularization in the rabbit model of congenital diaphragmatic hernia

Complex aneuploidy triggers autophagy and p53-mediated apoptosis and impairs the second lineage segregation in human preimplantation embryos

Complex aneuploidy triggers autophagy and p53-mediated apoptosis and impairs the second lineage segregation in human preimplantation embryos

Gain of 1q confers an MDM4-driven growth advantage to undifferentiated and differentiating hESC while altering their differentiation capacity

Lineage segregation in human pre-implantation embryos is specified by YAP1 and TEAD1

A conserved role of the Hippo signalling pathway in initiation of the first lineage specification event across mammals

Mitochondrial DNA variants segregate during human preimplantation development into genetically different cell lineages that are maintained postnatally

On the origins and fate of chromosomal abnormalities in human preimplantation embryos: an unsolved riddle

On the origins and fate of chromosomal abnormalities in human preimplantation embryos: an unsolved riddle

Sustained intrinsic WNT and BMP4 activation impairs hESC differentiation to definitive endoderm and drives the cells towards extra-embryonic mesoderm

Aneuploidy induces proteotoxic stress and autophagy-mediated apoptosis in human preimplantation embryos

Collaborators (18)

Anfien Huyghebaert

Kathy Niakan

Panagiotis Stamatiadis

Nusa Krivec

Hilde Van De Velde

Katrien Stouffs

Claire Simon

Greta Verheyen

Mary-Louise Bonduelle

Diana AlDelbany

Karen Sermon

Florence Belva

Pieter Verdyck

Stefaan Verhulst

Alexander Gheldof

willem verpoest

Sara Seneca

Claudia Spits

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