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Melanie A. Woodin

Researcher at University of Toronto

Publications -  60
Citations -  3582

Melanie A. Woodin is an academic researcher from University of Toronto. The author has contributed to research in topics: Inhibitory postsynaptic potential & Excitatory postsynaptic potential. The author has an hindex of 29, co-authored 57 publications receiving 3048 citations. Previous affiliations of Melanie A. Woodin include University of California, Berkeley & University of Calgary.

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Coincident Pre- and Postsynaptic Activity Modifies GABAergic Synapses by Postsynaptic Changes in Cl− Transporter Activity

TL;DR: It is reported that, in both hippocampal cultures and acute hippocampal slices, repetitive postsynaptic spiking within 20 ms before and after the activation of GABAergic synapses also led to a persistent change in synaptic strength.
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Neurons are recruited to a memory trace based on relative neuronal excitability immediately before training

TL;DR: The results indicate that neuronal memory allocation is based on relative neuronal excitability immediately before training, and that neurons with increased CREB are critical components of the memory trace.
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Single cell-derived clonal analysis of human glioblastoma links functional and genomic heterogeneity.

TL;DR: It is predicted that integration of functional and genomic analysis at a clonal level will be essential for understanding evolution and therapeutic resistance of human cancer, and will lead to the discovery of novel driver mechanisms and clone-specific cancer treatment.
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Single cell derived clonal analysis of human glioblastoma links functional and genomic heterogeneity.

TL;DR: The results suggest that functional clonal profiling used to identify tumorigenic and drug resistant tumor clones will lead to the discovery of new GBM clone-specific treatment strategies.
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Role of activity-dependent regulation of neuronal chloride homeostasis in development.

TL;DR: Evidence shows how both activity and neurotrophic factors can affect GABAergic transmission in the mammalian central nervous system through their effects on the neuron-specific chloride-extruding transporter KCC2, profoundly affecting the development and function of neuronal networks.