Workshop 5: Final phase
1 week; target groups: all ESRs/beneficiaries and partner organisations and scientific/industrial community (up to 60 participant)
This workshop is especially designed as an outreach project to present and discuss results of the ETN with the international community. It consists of an international 3-day conference inviting internationally renowned speakers with a satellite symposium on instrumentation for 1 day, and a 1-day programme on career development with a match-making opportunity for future employers of the private and academic sectors. Specific aspects within InCeM's scope to be addressed include the following:
Last update: 26.09.2018
September 5th, 2018
University of Sussex
Migrating primary keratinocyte with labelled cell adhesions. Based on a fine tuned regulation adhesion structures are continuously formed, modified and finally disassembled.
Primary keratinocytes apply traction forces upon migration. Using fluorescent fusion proteins (GFP-vinculin), adhesion structures can be visualized. Those sites are used by the cell for cell force transmission to the underlying substrate. In case those substrates are elastic, forces cause deformation fields that can be visualized using marker particles.
A typical example of the application of the evolving surface finite element method when solving partial differential equations of reaction-diffusion type on an evolving closed surface representing an evolving tumour.
A typical example of the application of the evolving surface finite element method when solving partial differential equations of reaction-diffusion type on an evolving open surface.
Time-lapse recordings of HK18-YFP fluorescence (left) of a migrating EK18-1 cell displaying multiple emerging KFPs in the proceeding lamellipodium. (Kölsch et al., 2010)
Induction of cell border dynamics through UV-light induced activation of pa-rac.
This project has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 642866.