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12,871 results for “aging;”

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zenodo28/100

Supplement to: Absolute age and temperature of belemnite rostra: constrains on the Early Cretaceous cooling event.

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opencc-by-4.0Dec 2023View details →
zenodo28/100

Figure 4 from: Obaid KA, Fawzi HA (2024) Evaluation of empagliflozin efficacy as a promising anti-aging treatment in mice: In-vivo study. Pharmacia 71: 1-9. https://doi.org/10.3897/pharmacia.71.e116184

Figure 4 Cross-sections of heart tissue of mice. A: In mice received normal saline only (G1); B: In mice received DGAL only (G2); C: In mice received DGAL and EMP 1 mg/kg after the end of induction (G4) (Olympus BX51microscpose and a software DP controller X40).

opencc-by-4.0Jan 2024View details →
zenodo28/100

Modeling cerebral hemodynamic parameters vs. age

<p>These data were consecutively collected at the Wroclaw University of Science and Technology from June 2014 to June 2015.</p> <p>The study participants were recruited and divided into two distinct groups. The younger group included patients aged from 18 years (only adults, no children or adolescents) up to 30 years. The older group (&gt; 40 years) has been designed as a subgroup to analyze more pronounced changes in structural and functional changes in cerebral arteries.</p> <p>Exclusion criteria were patients with any vascular risk factors (hypertension, smoking, diabetes mellitus, dyslipidemia, and cardiovascular or neurological diseases). None of the volunteers was under medications. Before the measurement was performed, the participants were instructed to abstain from consuming caffeine and alcohol and to avoid engaging in intensive exercise for at least 12 hours.</p> <h3><strong><span>Funding</span></strong></h3> <p><span><strong><span>SONATA 18&nbsp;</span></strong></span><span><strong><span>UMO-2022/47/D/ST7/00229 </span></strong></span><span>National Science Centre, Poland</span></p> <p><span><strong><span>SONATA-BIS UMO-2013/10/E/ST7/00117 </span></strong></span><span><span>National Science Centre, </span></span><span>Poland</span></p> <p><strong>If using this data, please refer to the following article:</strong></p> <p>Uryga A, Czosnyka M, Robba C, Nasr N, Kasprowicz M. The time constant of the cerebral arterial bed: exploring age-related implications. J Clin Monit Comput. 2024 Apr 4. doi: 10.1007/s10877-024-01142-5. PMID: 38573368.</p> <p>&nbsp;</p>

opencc-zeroFeb 2024View details →
zenodo28/100

Canagliflozin anti aging

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opencc-by-4.0Apr 2024View details →
zenodo28/100

PHYSIOLOGICAL CHARACTERISTICS OF ANEMIA IN PEOPLE OF DIFFERENT AGE

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opencc-by-4.0Nov 2024View details →
zenodo28/100

raw data - Estimated Pulse Wave Velocity and Osteoporosis in the Middle-aged and Elderly Population: An analysis from NHANES 2005-2020

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opencc-by-4.0Nov 2024View details →
zenodo28/100

THE ROLE OF THE BRONZE AGE SEDENTARY FARMING CULTURE IN THE WORK OF THE UZBEK ARCHAEOLOGIST AKHMADALI ASKAROV

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opencc-by-4.0Nov 2024View details →
zenodo28/100

Long-term monitoring reveals sex- and age-related survival patterns in griffon vultures

<p>Excel dataset</p>

opencc-by-4.0Nov 2024View details →
zenodo28/100

THE CULTURE OF THE STEPPE TRIBES OF THE BRONZE AGE OF LOWER ZARAFSHAN IN THE EARLY STUDIES OF AKHMADALI ASKAROV

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opencc-by-4.0Dec 2024View details →
zenodo28/100

The Influence of Study Quality, Age, and Geographic Factors on Polycystic Ovary Syndrome Prevalence-A Systematic Review and Meta-Analysis (Supplemental data)

<p><strong><span>Supplemnatray data for manuscript tentatively entitled "The Influence of Study Quality, Age, and Geographic Factors on </span></strong><strong><span>Polycystic Ovary Syndrome Prevalence</span></strong><strong><span>-A Systematic Review and Meta-Analysis", including:&nbsp;</span></strong></p> <p><strong><span>Supplementary Table 1.</span></strong><span> Search strategy and its results including studies published until February 29<sup>th</sup> of 2024.</span></p> <p><strong><span>Supplementary Table 2.</span></strong><span> The quality assessment results of studies conducted on adults based on the Polycystic ovary syndrome (PCOS) Epidemiology and Phenotype (PEP) tool. </span></p> <p><strong><span>Supplementary Table 3.</span></strong><span> The quality assessment results of studies conducted on adolescents based on <a name="_Hlk176077530"></a>the Polycystic ovary syndrome (PCOS) Epidemiology and Phenotype (PEP) tool. </span></p> <p><strong><span>Supplementary Table 4.</span></strong><span> The quality assessment results of studies conducted on mixed populations (both adults and adolescents) based on PCOS Epidemiology and Phenotype (PEP) tool. </span></p> <p><strong><span>Supplementary Figure 1 (A-D). </span></strong><span>Forest plots of global PCOS prevalence stratified by diagnostic criteria (regardless of study quality, age group, and geographic region): A) NIH, B) Rotterdam, C) AE-PCOS, D) Self-report: A) NIH, B) Rotterdam, C) AE-PCOS, D) Self-report.</span></p> <p><strong><span>Supplementary Figure 2 (A-C</span></strong><span>). Forest plots of global PCOS prevalence stratified by WHO region and diagnostic criteria (regardless of study quality and age group): A) NIH, B) Rotterdam, C) AE-PCOS.</span></p> <p><strong><span>Supplementary Figure 3 (A-C).</span></strong><span> </span><a name="_Hlk174390393"></a><span>Forest plots of PCOS prevalence stratified by diagnostic criteria and age group (adults vs. adolescent) (regardless of study quality): A) NIH, B) Rotterdam, C) AE-PCOS.</span></p> <p><strong><span>Supplementary Figure 4 (A-C).</span></strong><span> Sensitivity Analysis based on high-quality studies: Impact of individual study exclusion on pooled prevalence</span> <span>(using high-quality studies only)- A) NIH, B) Rotterdam, C) AE-PCOS.</span></p>

opencc-by-4.0Oct 2024View details →
zenodo28/100

Relate-estimated coalescence rates and allele ages for European beef cattle

<h1>Overview</h1> <p>Coalescence rates and allele ages calculated for five beef cattle breeds (Charolais, Simmental, Limousin, Hereford, Angus) using Relate.</p> <p>We estimated the joint genealogy of 684 individuals, including both <em>Bos taurus</em> and <em>Bos indicus</em>, then extracted the embedded genealogy for the five cattle breeds and re-estimated the population size history and branch lengths.</p> <p>We extracted the embedded genealogy for each of the five beef cattle breeds, jointly estimated the population size history, and re-estimated the branch lengths.</p> <p>Please email bft990914@163.com for any queries.</p> <h1>Coalescence Rates and Allele Ages</h1> <p>The *.coal files record coalescence rates for each of the five cattle breeds.</p> <p>The gzipped files allele_ages_*.gz record allele ages for each of the five cattle breeds.</p>

opencc-by-4.0Dec 2024View details →
zenodo28/100

Supplementary Data for "A Holocene n-alkane stable isotope sequence from Wonderwerk Cave, 1 South Africa and its implications for the Later Stone Age record"

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opencc-by-4.0May 2024View details →
zenodo28/100

Supplement video_Aging Skin Model

<p>Supplementary video&nbsp;for Aging Skin Model&nbsp;</p>

opencc-by-4.0Oct 2021View details →
dryad28/100

COVID-19 PHAC Agent-Based Model for age-stratified intervention and herd immunity study

<p>The PHAC agent-based model was used to explore the progression of the COVID-19 epidemic under three intervention scenarios (infection-preventing vaccination, illness-preventing vaccination and shielding) in individuals above three age thresholds (≥45, ≥55 and ≥65 years) while lifting shutdowns and physical distancing in the community. This data repository contains the PHAC modelling code in Anylogic used for this study. </p>

opencc-zeroNov 2021View details →
dryad28/100

Incubation temperature and physiological aging in the zebra finch

<p>In birds, incubation temperature has received increased attention as an important source of phenotypic variability in offspring. A lower than optimal incubation temperature may negatively affect aspects of nestling physiology, such as body growth and energy metabolism. However, the long-term effects of sub-optimal incubation temperature on morphology and physiology are not well understood. In a previous study, we showed that zebra finches from eggs incubated at a low temperature (35.9°C) for 2/3 of the total incubation time suffered a lower post-fledging survival compared to individuals that had been incubated at higher temperatures (37.0 and 37.9°C). In the present study, we investigated whether these variations in incubation temperature could cause permanent long-lasting differences in body mass, body size, or basal metabolic rate. Furthermore, we tested whether the observed differences in survival between treatment groups would be reflected in the rate of physiological deterioration, assessed through oxidative damage and decreased metabolic rate with age (i.e. 'metabolic aging'). Incubation temperature did not significantly affect embryonic or nestling body growth and did not influence final adult body mass or body size. Nor was there any long-term effect on basal metabolic rate. Birds from eggs incubated at the lowest temperature experienced an accumulation of oxidative damage with age, although this was not accompanied by an accelerated rate of metabolic aging. The present results suggest that the low survival in these birds was possibly mediated by increased oxidative stress, but independent of body growth and the basal metabolic rate.</p>

opencc-zeroNov 2021View details →
zenodo28/100

Fig. 3 in Efficiency Against The Two-Spotted Spider Mite Tetranychus Urticae And Prey-Age-Related Choice Of Three Predatory Mites

Fig. 3. Number of juvenile spider mites surviving in the presence of predatory mites at different predator densities. Light grey boxes represent treatments with low predator densities, dark grey boxes represent treatments with high predator densities. Boxes show the median and the 25–75 percentiles; dashed lines indicate the range

opencc-by-4.0Mar 2018View details →
zenodo28/100

Fig. 2 in Efficiency Against The Two-Spotted Spider Mite Tetranychus Urticae And Prey-Age-Related Choice Of Three Predatory Mites

Fig. 2. Number of spider mite eggs surviving in the presence of predatory mites at different predator densities. Light grey boxes represent treatments with low predator densities, dark grey boxes represent treatments with high predator densities. Boxes show the median and the 25–75 percentiles; dashed lines indicate the range

opencc-by-4.0Mar 2018View details →
zenodo28/100

Fig. 3 in Age, growth, and reproductive aspects of the dusky grouper Mycteroperca marginata (Actinopterygii: Epinephelidae) in a man-made rocky habitat in southern Brazil

Fig. 3. Age absolute frequency for the dusky grouper (Mycteroperca marginata) collected in the study area. n = 108.

opencc-by-4.0Oct 2011View details →
dryad28/100

Data on paternal age and sperm production of the progeny

<p>Parental age has profound consequences for offspring's phenotype. However, whether patrilineal age affects offspring sperm production is unknown, despite the importance of sperm production for male reproductive success in species facing post-copulatory sexual selection. Using a longitudinal dataset on ejaculate attributes of the houbara bustard, we showed that offspring sired by old fathers had different age-dependent trajectories of sperm production compared to offspring sired by young fathers. Specifically, they produced less sperm (-48%) in their first year of life, and 14% less during their lifetime. Paternal age had the strongest effect, with weak evidence for grandpaternal or great grandpaternal age effects. These results show that paternal age can affect offspring reproductive success by reducing sperm production, establishing an intergenerational link between aging and sexual selection.</p>

opencc-zeroDec 2021View details →
zenodo28/100

Supplementary material 1 from: Hall RM, Urban B, Skalova H, Moravcová L, Sölter U, Starfinger U, Kazinczi G, van Valkenburg J, Fenesi A, Konstantinovic B, Uludag A, Lommen S, Karrer G (2021) Seed viability of common ragweed (Ambrosia artemisiifolia L.) is affected by seed origin and age, but also by testing method and laboratory. NeoBiota 70: 193-221. https://doi.org/10.3897/neobiota.70.66915

Supporting tables and figures

opencc-zeroDec 2021View details →

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Allen Brain Atlas

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allen-brain-atlas
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Last verified 2026-04-30Open record

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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

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