Michael Magnussen
University of Copenhagen, University College London
Research areas: Biochemistry, Genetics and Molecular Biology · Molecular Biology · Acute Lymphoblastic Leukemia research · DNA Repair Mechanisms · Genomics and Chromatin Dynamics
About
I am a highly-interdisciplinary research scientist with 8 years of professional laboratory-based experience in academia. I am expert in using engineering principals to interpret and modulate tissue behaviours for generating innovative human models, or perturbing animal models of development, that are multiparametric and highly biomimetic. This interdisciplinary expertise stems from my time spent in 5 UK labs working on projects covering tissue engineering, cancer biology, and in silico data mining, yet above all has been honed on bioengineering and materials science for constructing innovative in vitro and in vivo developmental and disease modelling platforms. PhD program at UCL with an unprecedented £50K consumables budget. In the 4.5 years of my PhD I combined my engineering and biomaterials expertise with knowledge of stem cell biology to generate highly biomimetic models of embryonic heart development. By the culmination of my PhD, I had exposed new roles for embryogenic geometries and ECM accumulation in myocardial patterning in the embryonic heart.
Employment
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University of Copenhagen Post Doctoral Research Associate2022 - Present
Education
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University College London BHF 4-year Cardiovascular Biomedicine PhD2017 - 2022
Projects & Funding
Projects & funding information is unavailable.
Publications (8)
- Quantifying mechanical forces during vertebrate morphogenesis Save
- Hydrogel-in-hydrogel live bioprinting for guidance and control of organoids and organotypic cultures Save
- Timely delivery of cardiac mmRNAs in microfluidics enhances cardiogenic programming of human pluripotent stem cells. Save
- Quantifying mechanical forces during vertebrate morphogenesis Save
- Intravital three-dimensional bioprinting Save
- EZH2-Deficient T-cell Acute Lymphoblastic Leukemia Is Sensitized to CHK1 Inhibition through Enhanced Replication Stress. Save
- Beyond Family: Modeling Non-hereditary Heart Diseases With Human Pluripotent Stem Cell-Derived Cardiomyocytes. Save
- Activation of the LMO2 oncogene through a somatically acquired neomorphic promoter in T-cell acute lymphoblastic leukemia. Save