News

What factors can help prevent warring parties from reverting to violence and instead create a sustainable peace? This is the central question at the heart of the PhD thesis ‘Sustainable Peacebuilding in Divided Societies’ defended by Ayokunu Adedokun on 20 December 2016.

Students at Maastricht University have developed a device that can detect the presence of certain bacteria. This device may help to prevent bacterial outbreaks in the future.

On Wednesday, 13 July 2016 the first 10 bachelor's students to complete the work/study track KnowledgeEngineering@Work, a programme unique in the Netherlands,  graduated.

Principal components analysis (PCA) is a common unsupervised method for the analysis of gene expression microarray data, providing information on the overall structure of the analyzed dataset. 

MaCSBio's director of education Bert Smeets has been interviewed for the Dutch serie: 'Research Loont' (translation: 'Research pays off') about the unraveling of genetic causes of hereditary metabolic disease among children.

Neurogenesis is the process by which new neurons are generated from neural stem cells and progenitor cells which takes place continuously throughout our life. In this work the interdisciplinary team with Gökhan Ertaylan of MaCSBio has been collaborating, uncovers a function for Prox1 gene that functions as an inducer of neuronal differentiation.

Michelle Moerel from MaCSBio has been on the most famous educational tv-show for kids in The Netherlands ( Het Klokhuis ) to explain how the human brain works.

PhD-candidate Shauna O’Donovan has won a prize for best poster at the byteMAL Conference held on March 9th in Maastricht. Her poster subject was on improving the muscle insulin sensitivity index using the oral glucose minimal model.

Theo de Kok will give his Inaugural Lecture, entitled “Genes in Concert: a Toxicogenomics Hymn towards disease prevention” on Friday 22 April 2016. The lecture will take place at the University Auditorium - MBB. Time: 16:30

MaCSBio’s Mike Gerards was involved as a senior author in an article entitled “Novel pathogenic SLC25A46 splice-site mutation causes an optic atrophy spectrum disorder.” which was published in “Clinical Genetics”.