Corey M. McCann
Harvard University
7 Papers
82 Citations
Corey M. McCann is an academic researcher from Harvard University. The author has contributed to research in topics: Postsynaptic density & Synapse. The author has an hindex of 7, co-authored 7 publications.
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Papers
Rapid synapse elimination after postsynaptic protein synthesis inhibition in vivo.
TL;DR: Structural similarities between this process and naturally occurring synapse elimination suggest that short-lived target derived factors not only participate in synaptic maintenance in adults, but also regulate elimination of connections during development.
Rapid and modifiable neurotransmitter receptor dynamics at a neuronal synapse in vivo
TL;DR: Imaged the synapses between pre- and postganglionic neurons in the mouse submandibular ganglion in vivo, focusing on the mechanisms that maintain and regulate neurotransmitter receptor density at postsynaptic sites, to show that neurotransmitter receptors dynamism associated with rapid changes in synaptic efficacy precedes long-lasting structural change in synaptic connectivity.
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In vivo imaging of presynaptic terminals and postsynaptic sites in the mouse submandibular ganglion
Corey M. McCann,Jeff W. Lichtman +1 more
TL;DR: In vivo methods to acquire three‐dimensional image stacks of the axons and postsynaptic sites and then follow them over time are developed to study the formation, elimination, and maintenance of synaptic connections between neurons in vivo.
Combined magnetic resonance and fluorescence imaging of the living mouse brain reveals glioma response to chemotherapy.
Corey M. McCann,Peter Waterman,Jose-Luiz Figueiredo,Elena Aikawa,Ralph Weissleder,John W. Chen +5 more
TL;DR: It is shown that FMT-MR imaging can produce three-dimensional, multimodal images of living mouse brains allowing for serial monitoring of tumor morphology and protease activity, and that combined FMT and magnetic resonance imaging of fluorescent molecular probes could be valuable for brain tumor drug development and other neurological and somatic imaging applications.
Peptide tags for labeling membrane proteins in live cells with multiple fluorophores.
TL;DR: This strategy for epitope tagging provides a useful adjunct to green fluorescent protein (GFP)-tagging, which fails to distinguish intracellular from extracellular pools, sometimes interferes with protein localization or function, and requires a separate construct for each color.