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Megan Crow

Researcher at Cold Spring Harbor Laboratory

Publications -  35
Citations -  2055

Megan Crow is an academic researcher from Cold Spring Harbor Laboratory. The author has contributed to research in topics: Cell type & Gene. The author has an hindex of 15, co-authored 31 publications receiving 1165 citations. Previous affiliations of Megan Crow include Wolfson Centre for Age-Related Diseases.

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Transcriptional Architecture of Synaptic Communication Delineates GABAergic Neuron Identity.

TL;DR: It is discovered that cardinal GABAergic neuron types are delineated by a transcriptional architecture that encodes their synaptic communication patterns and forms a multi-layered molecular scaffold along the cell membrane that may customize synaptic connectivity patterns and input-output signaling properties.
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Comparative cellular analysis of motor cortex in human, marmoset and mouse

Trygve E. Bakken, +121 more
- 01 Oct 2021 - 
TL;DR: The primary motor cortex (M1) is essential for voluntary fine-motor control and is functionally conserved across mammals using high-throughput transcriptomic and epigenomic profiling of more than 450k single nuclei in humans, marmoset monkeys and mice as mentioned in this paper.
Posted ContentDOI

A multimodal cell census and atlas of the mammalian primary motor cortex

Ricky S. Adkins, +247 more
- 07 Oct 2021 - 
TL;DR: This study reveals a unified molecular genetic landscape of cortical cell types that congruently integrates their transcriptome, open chromatin and DNA methylation maps, and establishes a unified and mechanistic framework of neuronal cell type organization that integrates multi-layered molecular genetic and spatial information with multi-faceted phenotypic properties.
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Characterizing the replicability of cell types defined by single cell RNA-sequencing data using MetaNeighbor.

TL;DR: This work develops MetaNeighbor for measuring cell-type replication across datasets, and uses it to identify marker genes for neuron subtypes with evidence of replication, and finds that large sets of variably expressed genes can identify replicable cell types with high accuracy.
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HDAC inhibitors attenuate the development of hypersensitivity in models of neuropathic pain

TL;DR: Data support a role for histone acetylation in the emergence of neuropathic pain and suggest that this effect may be mediated at the level of the spinal cord through inhibition of HDAC1 function.