ReviewThe Journal of endocrinology2026
Clocks on steroids: how glucocorticoid receptors tell cells the time.
Review in The Journal of endocrinology, 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.
- Circadian regulation of osteoclast lysosomal-resorption machinery: implications for osteoporosis therapy.Frontiers in cell and developmental biology · 2026Review
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
No grant is acknowledged in the PubMed record.
Abstract
Glucocorticoid (GC) steroid hormone signalling via the glucocorticoid receptor (GR) underlies most daily physiological rhythms in mammals by synchronising cellular circadian rhythms throughout the body. Impaired circadian synchrony is associated with many non-communicable diseases, such as cardiovascular disease, diabetes and cancer. The functions and daily regulation of systemic GC levels are relatively well understood, yet a clearly defined mechanism for GC/GR-mediated circadian synchronisation is lacking. Historically, mechanistic studies of GR action have focused on its role as a transcription factor, sufficient to explain many, but not all, consequences of GC/GR signalling. Recently, several non-canonical modes of GR action have been described and proposed as a basis for understanding rapid cellular responses to GCs that cannot be explained by relatively slow changes in transcription. Here, we review the current state of knowledge on the cellular mechanism of GR signalling in the context of GR-mediated circadian synchronisation, outline gaps in current understanding and suggest new avenues for investigation.
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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.