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307 results for “circadian rhythms”

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ClinicalTrials.gov32/100

Investigating Circadian Rhythms in Youth With Persistent Tic Disorders

ClinicalTrials.gov study NCT03508245. IPD Sharing: NO. Countries: 1. Publications: 3.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Effects of Kangaroo Care on Circadian Rhythm, Growth and Physiological Effects

ClinicalTrials.gov study NCT06589349. IPD Sharing: NO. Countries: 1. Publications: 4.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Aspirin AM or PM: Effect on Circadian Rhythm of Platelet Reactivity

ClinicalTrials.gov study NCT01900639. IPD Sharing: Not stated. Countries: 1. Publications: 5.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

A Cohort Study on Treating Primary Nocturnal Enuresis by Regulating Central-Peripheral Circadian Rhythm

ClinicalTrials.gov study NCT07003126. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

The Daytime Circadian Rhythm in Exhaled Volatile Organic Compounds in People Living Without and Diabetes

ClinicalTrials.gov study NCT05984979. IPD Sharing: NO. Countries: 1. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Circadian Rhythm Disruption in the Hospital Intensive Care Environment

ClinicalTrials.gov study NCT05828680. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

Factors Associated With Infant Circadian Rhythm, Growth, and Temperament

ClinicalTrials.gov study NCT05700136. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

"Cancersensor": Circadian Rhythms

ClinicalTrials.gov study NCT01693835. IPD Sharing: Not stated. Countries: 1. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

Circadian Rhythms and Sleep in Familial DSPS and ASPS

ClinicalTrials.gov study NCT00246454. IPD Sharing: NO. Countries: 1. Publications: 6.

closedIPD-NOFeb 2026View details →
dryad32/100

Data from: Optimal sampling interval for characterisation of the circadian rhythm of body temperature in homeothermic animals using periodogram and cosinor analysis

Open the record for dataset details and reuse information.

publicMar 2024View details →
dryad32/100

Arginine-vasopressin expressing neurons in the murine suprachiasmatic nucleus exhibit a circadian rhythm in network coherence in vivo

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publicJan 2023View details →
dryad32/100

Characterizing the modern light environment and its influence on circadian rhythms

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publicJul 2021View details →
dryad32/100

Data from: Developmental exposure to PCB153 (2,2’,4,4’,5,5’-hexachlorobiphenyl) alters circadian rhythms and the expression of clock and metabolic genes

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publicNov 2019View details →
dryad32/100

Data from: Circadian rhythms vary over the growing season and correlate with fitness components

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publicJul 2017View details →
dryad32/100

Superoxide is promoted by sucrose and affects amplitude of circadian rhythms in the evening

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publicFeb 2021View details →
zenodo28/100

Figure 2 from: Krichilsky E, Vega-Hidalgo Á, Hunter K, Kingwell C, Ritner C, Wcislo W, Smith A (2020) The first gynandromorph of the Neotropical bee Megalopta amoena (Spinola, 1853) (Halictidae) with notes on its circadian rhythm. Journal of Hymenoptera Research 75: 97-108. https://doi.org/10.3897/jhr.75.47828

Figure 2 Single-plot actogram of four days of activity in dark-dark conditions showing a female, the gynandromorph, and a male M. amoena. Each bar represents the amount of times that the bee crossed the laser in a 15 minute interval. White space indicates lack of activity.

opencc-by-4.0Mar 2020View details →
zenodo28/100

Figure 1 from: Krichilsky E, Vega-Hidalgo Á, Hunter K, Kingwell C, Ritner C, Wcislo W, Smith A (2020) The first gynandromorph of the Neotropical bee Megalopta amoena (Spinola, 1853) (Halictidae) with notes on its circadian rhythm. Journal of Hymenoptera Research 75: 97-108. https://doi.org/10.3897/jhr.75.47828

Figure 1 A Frontal view of the head showing the bilateral split between sexes (female left side of image, male right side) B detail of female (left) and male (right) mandibles and labrum, frontal view. Lateral view of the C male and D female genae and mandibles E ventral view of gynandromorph (female left side of image, male right side). Femur, apical spines, and tibia of F male and G female hindlegs H dorsal view of stinger I ventral view of metasoma (female left side of image, male right side). Scale bars: 500 μm.

opencc-by-4.0Mar 2020View details →
dryad28/100

Data from: Eyeless Mexican cavefish save energy by eliminating the circadian rhythm in metabolism

The eyed surface form and eyeless cave form of the Mexican tetra Astyanax mexicanus experience stark differences in the daily periodicities of light, food and predation, factors which are likely to have a profound influence on metabolism. We measured the metabolic rate of Pachón cave and surface fish at a fixed swimming speed under light/dark and constant dark photoperiods. In constant darkness surface forms exhibited a circadian rhythm in metabolism with an increase in oxygen demand during the subjective daytime, whereas cave forms did not. The lack of circadian rhythm in metabolism leads to a 27% energy savings for Pachón cave fish compared to surface fish when comparing both forms in their natural photoperiods. When surface forms were tested under constant dark conditions they expended 38% more energy than cave forms under equivalent conditions. Elimination of the circadian rhythm in metabolism may be a general feature of animals that live in perpetually dark food-limited environments such as caves or the deep sea.

opencc-zeroDec 2013View details →
dryad28/100

Data from: Costs of sleeping in: circadian rhythms influence cuckoldry risk in a songbird

1. Circadian (i.e. daily) regulation of behaviors is thought to provide fitness benefits to organisms by enabling them to anticipate diel changes in the environment, such as sunrise. 2. A common behavior among socially monogamous songbirds that usually takes place in the early mornings is extra-pair mating, i.e. copulating with partners outside of the social pair bond. 3. Thus, variation in when individuals begin their daily activity may influence their reproductive success; early risers may be better able to gain copulations guard their partners thus minimizing their risk of being cuckolded compared to late risers. Sexual selection may thus play an important role in shaping circadian behaviors, but this assumption has yet to be tested in free-living animals. 4. Here we experimentally weakened endogenous circadian rhythmicity and thus anticipation of dawn in male great tits (Parus major) in the wild through the subcutaneous administration of implants filled with melatonin shortly before egg-laying began in this population; melatonin is a hormone released during the dark phase of the day, and is one important cue animals use to entrain their circadian clock. 5. Experimental individuals delayed onset of daily activity compared with controls, and were more likely to be cuckolded compared with control males. Manipulation did not alter other behavioral traits observed; no difference between treatments was observed in activity levels during the day or in the end time of daily activity. 6. These results strongly support the assumption that selection, particularly sexual selection, shapes circadian phenotypes of wild vertebrates which enable anticipation of important and predictive diel changes in an individual's biotic and abiotic environment.

opencc-zeroDec 2014View details →
zenodo28/100

Figure 6 from: Espinasa L, Collins E, Finocchiaro A, Kopp J, Robinson J, Rutkowski J (2016) Incipient regressive evolution of the circadian rhythms of a cave amphipod. Subterranean Biology 20: 1-13. https://doi.org/10.3897/subtbiol.20.10010

Figure 6 - Stygobromus allegheniensis has continuous light avoidance behavior which does not appear to follow circadian rhythmicity. White boxes indicate illuminated conditions.

opencc-by-4.0Oct 2016View details →

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Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record