This project focuses on how germ cells control the function of Sertoli cells.

This study aims to identify and understand mechanisms of intrinsic and acquired resistance to RNA Polymerase I (Pol I) inhibition in cancer, with the goal of developing strategies to overcome resistance to Pol I inhibitors.

This project investigates antibacterial activites of newly developed biomaterials.

This project includes cellular immunology techniques, bioinformatics and biophysical techniques.

This study explores how dynamic changes in ribosomal DNA (rDNA) chromatin contribute to cancer development, aiming to uncover mechanisms of malignant transformation and potential therapeutic targets.

This project focuses on the role of H2A.B in spermatogenesis under heat stress.

This project focuses on novel morphometric analysis methods for emerging types of 3D image data.

Our research focuses on inhibiting nucleic acid sensing receptors or signaling pathway molecules to prevent autoantibody production and autoimmune pathology in autoimmune mouse models, in collaboration with the Gantier Group at the Hudson Institute of Medical Research.

We investigate cytokine roles in SLE and opportunities for projects studying their impact on autoreactive B cell survival, focusing on identified genetic variants and therapeutic targets.

The aim of this project is to better understand how the bacteria defend against viral infection and how we can take advantage of the bacteria defence system to harness it as a gene editing technology.

This study aims to develop effective combination therapies using RNA Polymerase I (Pol I) inhibitors to enhance therapeutic efficacy and combat resistance in cancer treatment through synergistic effects with other drugs or treatments.

This project focuses on understanding the role of WNT in congenital heart defects.

This study evaluates UBF (Upstream Binding Factor) as a potential target for cancer therapy by investigating its role in cancer cell growth and survival.

This project uses next generation sequencing (NGS) and mass spectrometry to investigate the possible existence of regulatory interactions between ribonucleic acids, enzymes and metabolites to connect gene expression and metabolism

The aim of this project is to understand the ways in which astrocytes can sense the activity at adjacent synapses and how in-turn they can release substances that modulate these synapses.