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Stephanie Shiers

Researcher at University of Texas at Dallas

Publications -  51
Citations -  1076

Stephanie Shiers is an academic researcher from University of Texas at Dallas. The author has contributed to research in topics: Nociceptor & Biology. The author has an hindex of 11, co-authored 34 publications receiving 372 citations.

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Spatial transcriptomics of dorsal root ganglia identifies molecular signatures of human nociceptors

TL;DR: In this article , the authors used spatial transcriptomics to molecularly characterize transcriptomes of single dorsal root ganglia (DRG) neurons from eight organ donors, identifying 12 clusters of human sensory neurons, 5 of which are C nociceptors, as well as 1 C low-threshold mechanoreceptors (LTMRs), 1 Aβ nocicusor, 2 Aδ,2 Aβ, and 1 proprioceptor subtypes.
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Quantitative differences in neuronal subpopulations between mouse and human dorsal root ganglia demonstrated with RNAscope in situ hybridization

TL;DR: Insight is offered into the spatial and functional organization of neuronal cell subpopulations in the rodent and human DRG and support the idea that sensory system organizational principles are likely different between both species.
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Neurobiology of SARS-CoV-2 interactions with the peripheral nervous system: implications for COVID-19 and pain

TL;DR: In this paper, the authors discuss how COVID-19 may interact with the peripheral nervous system to cause pain in the early and late stages of the disease and the implications of this potential neurotropism.
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ACE2 and SCARF expression in human dorsal root ganglion nociceptors: implications for SARS-CoV-2 virus neurological effects.

TL;DR: DRG sensory neurons are a potential target for SARS-CoV-2 invasion of the peripheral nervous system and viral infection of human nociceptors may cause some of the persistent neurological effects seen in COVID-19.
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A Critical Role for Dopamine D5 Receptors in Pain Chronicity in Male Mice.

TL;DR: The work demonstrates that dopaminergic spinal projections are necessary for the maintenance of a chronic pain state in both sexes; however, D5 receptors seem to play a critical role in males whereas females rely more heavily on D1 receptors, an effect that could be explained by sexual dimorphisms in receptor expression levels.