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Control of CBP functions by calcium signalling pathways in neurons


The aim of this work is to determine molecular domains and phosphorylation sites involved in the regulation of CBP transactivating properties upon Ca(2+) stimulation in neuronal cells. I will also assess the role of CBP's histone acetyl transferase activity in Ca(2+-)activated gene expression.

Funding Scheme

RGI - Research grants (individual fellowships)


MRC Laboratory of Molecular Biology
Hills Road
CB2 2QH Cambridge
United Kingdom

Participants (1)

Not available