ArticleBiology methods & protocols2026
Cannabinoid GPCRs, ectopic olfactory GPCRs and TRP channels: a prespecified baseline-edit-rescue framework for testing higher-order membrane-conditioned integration.
Article in Biology methods & protocols, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- The Endoterpenoid System: A Membrane-Based Logic Framework for Integrating Cannabinoid, Olfactory, and Lipid-Sensitive Receptor Crosstalk.Journal of neuroscience research · 2026Review
- Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Cell membranes are not mere platforms for signalling proteins; they can shape how receptor inputs are assembled into local responses. In membrane-rich microdomains, receptor identification and pathway mapping do not reveal the logic of a measured effect. That effect may arise from independent receptor activity, pairwise crosstalk or higher-order integration governed by membrane state. The membrane-encoded chemosensory system (MECS) is introduced as a conceptual framework for addressing the inferential gap between receptor co-expression mapping and mechanistic crosstalk claims in territories with cannabinoid GPCRs, ectopic olfactory GPCRs and TRP channels. Its operational method, MECS baseline-edit-rescue (MECS-BER), fixes one membrane prior, one locked proximal outcome and one three-arm candidate assembly. Eligibility gates test arm engagement and outcome competence. Combinatorial responses are analysed with κ, the third-order interaction under a pairwise-only null within a complete three-factor perturbation design, to distinguish lower-order explanation from higher-order interpretation and test edit-rescue reversibility. Deterministic matrices and simulations establish classification logic and tolerance handling; biological adjudication awaits fully compliant MECS-BER datasets. The workflow provides a prespecified and formalized methodological route, not biological proof of any specific receptor triad. It keeps nomination separate from adjudication and requires co-localization, distal phenotypes, shared downstream signals and nonlinear mixtures to be tested against a locked proximal outcome before biological interpretation. Renal micro-niches specify prospective deployment across renin, transport, barrier and flow-sensitive calcium control without claiming validated cannabinoid-olfactory-TRP assemblies. Membrane lipids may shape both the signalling vocabulary of individual receptors and the local language through which receptors communicate.
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What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.