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. The methods that we will develop will be generalizable to every miRNA, therefore allowing a widespread exploration of miRNA/target functions
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target for therapeutic intervention. This PhD project aims to develop nanobodies - single domain antibodies derived from camelid immunoglobulins - targeting GC-C for both therapeutic and structural
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their clinical utility. The thesis will develop novel mathematical approaches to identify re-entrant circuits using minimal, routinely acquired clinical data, specifically activation-time maps and atrial surface
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