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Michael J. Vasek

Researcher at Washington University in St. Louis

Publications -  16
Citations -  921

Michael J. Vasek is an academic researcher from Washington University in St. Louis. The author has contributed to research in topics: Microglia & RNA-binding protein. The author has an hindex of 8, co-authored 15 publications receiving 656 citations.

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A complement–microglial axis drives synapse loss during virus-induced memory impairment

TL;DR: It is shown that viral infection of adult hippocampal neurons induces complement-mediated elimination of presynaptic terminals in a murine WNV neuroinvasive disease model, which provides a new murine model of WNV-induced spatial memory impairment, and identifies a potential mechanism underlying neurocognitive impairment in patients recovering from WNV Neuroinvasive Disease.
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Astrocytes locally translate transcripts in their peripheral processes.

TL;DR: It is demonstrated that astrocytes also have sequence-dependent local translation in their peripheral processes, including transcripts with roles in regulating synapses, and one mechanism regulating this translation is identified, suggesting localtranslation inAstrocyte processes may play a role in synapse modulation.
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Astrocytes decrease adult neurogenesis during virus-induced memory dysfunction via IL-1.

TL;DR: It is shown, in a mouse model of West Nile virus–induced cognitive dysfunction, that neurogenesis is impaired by production of IL-1 from pro-inflammatory astrocytes, which might underlie the long-term cognitive consequences of WNND but also provides a therapeutic target.
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Diverse voltage-sensitive dyes modulate GABAA receptor function

TL;DR: The dual effects of voltage-sensitive dyes on GABAergic inhibition require caution in dye use for studies of excitability and network activity.
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Self-Reporting Transposons Enable Simultaneous Readout of Gene Expression and Transcription Factor Binding in Single Cells

TL;DR: This work presents self-reporting transposons (SRTs) and uses scCC, which map SRTs from scRNA-seq libraries, simultaneously identifying cell types and TFBS in those same cells, establishing a new method for studying TF biology in situ.