Emily Osterweil – Projects — University of Edinburgh Research Explorer

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Identifying mistranslating mRNAs in Fmr1-/y and Syngap+/- models of ASD/ID
Osterweil, E.
Medical Research Council
1/08/19 → 31/05/23
Project: Research
Identifying mistranslating mRNAs in Fmr1-/y and Syngap+/- models of ASD/ID
Osterweil, E.
MRC
1/08/19 → 31/05/23
Project: Research
Syn2Psy: Synaptic Dysfunction in Neuropsychiatric Disorders
Kind, P. & Osterweil, E.
European Commission
1/03/19 → 31/08/23
Project: Research
Synaptic Dysfunction in Neuropsychiatric Disorders
Kind, P. & Osterweil, E.
EU government bodies
1/03/19 → 30/04/23
Project: Research
Targeting the ubiquitin proteasome system in ASD/ID
Osterweil, E.
Non-EU industry, commerce and public corporations
7/01/19 → 6/04/20
Project: Research
Correcting the core pathophysiological deficits in the mouse model of Fragile X Syndrome through NMDA receptor modulation
Osterweil, E.
UK-based charities
15/05/17 → 7/07/17
Project: Research
Enhancement of NMDA receptor signalling for the treatment of fragile X syndrome
Osterweil, E.
Non-EU-based charities
1/08/16 → 31/07/18
Project: Research
Differential synaptic mRNA translation through ERK and mTOR signalling pathways
Osterweil, E.
UK-based charities
1/05/15 → 28/02/17
Project: Research
Targeting ERK and mTOR for the treatment of fragile X syndrome
Osterweil, E.
MRC
1/12/14 → 31/12/18
Project: Research
Differential regulation of protein synthesis in synaptic plasticity and autism spectrum disorders with associated intellectual disability (ASD/ID)
Osterweil, E.
UK-based charities
1/09/14 → 30/11/19
Project: Research
Differential regulation of protein synthesis in synaptic plasticity and autism spectrum disorders with associated intellectual disability (ASD/ID)
Osterweil, E.
Wellcome Trust (Rcl)
1/09/14 → 30/11/19
Project: Research