ReviewPain2026
Neurobiology of the trigeminal ganglion in comparison to the dorsal root ganglion.
Review in Pain, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
abstractThe trigeminal ganglion (TG) represents the craniofacial counterpart of the dorsal root ganglion (DRG) in the peripheral nervous system (PNS). TG and DRG are clusters of cell bodies of highly specialized sensory neurons, with TG neurons innervating the head and face and DRG neurons innervating the body. TG and DRG neurons are essential for detecting various mechanical, thermal, and chemical stimuli and relaying these internal or external signals to the central nervous system (CNS). Despite sharing fundamental similarities, TG and DRG differ significantly in many aspects under pathophysiological states. This review provides a comparison between these 2 types of ganglia by highlighting their distinctions across anatomical locations, embryological origins, cellular compositions, gene expression profiles and molecular signatures, ratios of A/C fibers, connections with the CNS, sympathetic fiber sprouting, ectopic discharges, biophysical properties of ion channels, and neuron-glia interactions. These divergences may contribute to certain differences in intensities and responses to the same stimuli or treatments between TG- and DRG-mediated pain. Acknowledging their neurobiological distinctions underscores the importance of identifying potential pain targets within each system independently and developing targeted therapeutic strategies for craniofacial vs somatic pain.
Indexed as
Identifiers
What OpenQuestion 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 OpenQuestion graph.