Studying the eukaryotic genome in 3D
Three-dimensional (3D) organisation of the eukaryotic nuclear genome has a crucial role in gene regulation. Magda Bienko and Nicola Crosetto overview emerging and established techniques used to investigate the spatial arrangement of the genome in the nucleus and how it affects gene function in single cells and tissues. Tight packing into chromatin fibers and their […]

HT and Bicocca collaborate on grant winning research on rare diseases
A research project focussing on rare diseases by Prof. Silvia Nicolis, in the Department of Biotechnology and Biosciences at the University of Milan Bicocca, in collaboration with Veronica Krenn, young researcher among the five winners of the first edition of HT’s Early Career Fellowship (ECF) Programme, and Prof. Giuseppe Testa, Head of the HT’s Neurogenomics […]
Marie Skłodowska-Curie Actions Postdoctoral Fellowships 2022 at HT
Human Technopole is looking for enthusiastic postdoctoral researchers interested in applying for Marie Skłodowska-Curie Actions Postdoctoral Fellowships 2022. Projects should focus on one of the areas of the five HT’s Research Centres: Computational Biology, Structural Biology, Genomics, Neurogenomics and Health Data Science. The objective of PFs is to support researchers’ careers and foster excellence in […]
Post-translational modifications in control of human thyroglobulin
Thyroglobulin is the protein precursor of thyroid hormones, key regulators of vertebrate development and metabolism. On the occasion of World Thyroid Day, Laura Tosatto and Francesca Coscia discuss how post-translational modifications (PTM) of thyroglobulin can regulate thyroid gland function in health and disease. They also highlight the importance of combining structural biology, proteomics, and genomics […]
HT Welcomes ISTA to Discuss New Frontiers in Life Sciences
The leadership of the Institute of Science and Technology Austria-ISTA is visiting Human Technopole for a day of talks and seminars. Thanks to the use of organoids, Human Technopole’s Centre for Neurogenomics and ISTA have already collaborated on a study on autism spectrum disorder caused by mutations in the CHD8 gene, recently published in the […]