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Persistent nociceptor hyperactivity as a painful evolutionary adaptation

Trends in Neurosciences(2023)10.1016/j.tins.2022.12.007Source: DataRank Database

Persistent nociceptor hyperactivity as a painful evolutionary adaptation is a research paper published in Trends in Neurosciences (2023). On theSindex it has a DataRank of 0. It has been cited 83 times.

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Open Access83 citations

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Enrichment:Funding (14 grants)Impact (FWCI 17.26)OA: greenTopics (35)Linked Datasets (25)DataCite Reuse (25)IDs (PubMed, OpenAlex)SDGs (1)

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Context only (not used in score)

Findable (2/2)

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Accessible (1/2)

Open Access

Interoperable (2/2)

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Reusable (0/3)

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Authors (5)

Robyn J. Crook ORCID,G. Gregory Neely ORCID,Theodore J. Price ORCID,Ewan St. John Smith ORCID,Edgar T. Walters ORCID

Live enrichment

PubMed:36610893 OpenAlex:https://openalex.org/W4313549723

National Health and Medical Research Council

Grant: APP1046090

National Health and Medical Research Council

Grant: APP1028887

National Health and Medical Research Council

Grant: APP1026310

Medical Research Council

Grant: MR/W002426/ 1

NIH

Grant: NS111929

NIH

Grant: NS091759

NIH

Grant: NS102161

NIH

Grant: RO1NS111521

National Science Foundation

Grant: IOS 204-7331

NINDS NIH HHS

Grant: R01 NS111521

NINDS NIH HHS

Grant: R01 NS111929

NINDS NIH HHS

Grant: R01 NS091759

NINDS NIH HHS

Grant: R01 NS102161

Cancer Research UK

Grant: 22053

FWCI

17.26

Citation Percentile

1.0%

Citation Trend

2023

2024

2025

2026

greenLicense: cc-by-nc-nd

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC9974896/pdf/nihms-1859675.pdf

publisherhttps://api.elsevier.com/content/article/PII:S0166223622002612?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S0166223622002612?httpAccept=text/plain

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/9974896

Fields of Study

Pain Mechanisms and TreatmentsHeart Rate Variability and Autonomic ControlStress Responses and CortisolHumansAnimalsNociceptorsSensory Receptor CellsNeuralgiaAdaptation, Physiological

MeSH Terms

Adaptation, PhysiologicalAnimalsHumansNeuralgiaNociceptorsSensory Receptor Cells

Keywords

NociceptorNeuroscienceNeuropathic painNociceptionChronic painDiseaseMedicineSensory systemAdaptation (eye)Noxious stimulusInflammationPsychologyPathologyReceptorInternal medicineAplysiacephalopodhumanprimary afferent neuronspontaneous activity

Sustainable Development Goals

SDG 0: Good health and well-being

Additional file 26 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 24 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 19 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 23 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 17 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 14 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 13 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 10 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 13 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 9 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 7 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 8 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 4 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 20 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 22 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 19 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 21 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 18 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

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Additional file 17 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

10.6084/m9.figshare.26755354.v1figshare

Additional file 14 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling

10.6084/m9.figshare.26755345.v1figshare

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