We are testing a new system for linking grants to scientists.
The funding information displayed below comes from the
NIH Research Portfolio Online Reporting Tools and the
NSF Award Database.
The grant data on this page is limited to grants awarded in the United States and is thus partial. It can nonetheless be used to understand how funding patterns influence mentorship networks and vice-versa, which has deep implications on how research is done.
You can help! If you notice any innacuracies, please
sign in and mark grants as correct or incorrect matches.
Sign in to see low-probability grants and correct any errors in linkage between grants and researchers.
High-probability grants
According to our matching algorithm, Heather Decot is the likely recipient of the following grants.
Years |
Recipients |
Code |
Title / Keywords |
Matching score |
2016 — 2017 |
Decot, Heather Kaye |
F31Activity Code Description: To provide predoctoral individuals with supervised research training in specified health and health-related areas leading toward the research degree (e.g., Ph.D.). |
Coordination of Brain Network Dynamics by Dopaminergic Activity @ Univ of North Carolina Chapel Hill
? DESCRIPTION (provided by applicant): Ventral Tegmental Area (VTA) dopaminergic neurons encode reward prediction errors and signal the incentive salience of sensory cues (1-3). Burst firing of these neurons result in phasic dopamine release in cortical and limbic terminal fields such as the medial prefrontal cortex (mPFC) and nucleus accumbens (NAc), which acts to modulate postsynaptic neuronal firing (7) to promote changes in motivated behavioral output (8-10). However, it remains unclear how VTA dopaminergic activity affects large-scale brain network functional connectivity, and how these brain network dynamics are altered following repeated cocaine self-administration. To address this, we will utilize a highly innovative approach that couples optogenetic stimulation techniques with functional magnetic resonance imaging (fMRI) technology in an in vivo rat model to determine whether selective stimulation of VTA dopaminergic neurons alters functional connectivity between multiple, anatomically distinct brain regions. The experiments proposed in this application would further our understanding on how aberrant dopaminergic signaling may degrade optimal neuronal network dynamics, which in turn may shift brain activity to promote maladaptive states.
|
0.946 |