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4,215 results for “high risk”
A Study of MBG453 in Combination With Hypomethylating Agents in Subjects With IPSS-R Intermediate, High or Very High Risk Myelodysplastic Syndrome (MDS).
ClinicalTrials.gov study NCT03946670. IPD Sharing: YES. Countries: 17. Publications: 1.
Adjuvant Ribociclib With Endocrine Therapy in Hormone Receptor+/HER2- High Risk Early Breast Cancer
ClinicalTrials.gov study NCT03078751. IPD Sharing: YES. Countries: 1. Publications: 1.
Intervention to Improve Driving Practices Among High-Risk Teen Drivers
ClinicalTrials.gov study NCT04317664. IPD Sharing: YES. Countries: 1. Publications: 17.
Safety, Tolerability, and Effect of Alirocumab in High Cardiovascular Risk Patients With Severe Hypercholesterolemia Not Adequately Controlled With Conventional Lipid-modifying Therapies (ODYSSEY APPR
ClinicalTrials.gov study NCT02476006. IPD Sharing: YES. Countries: 16. Publications: 1.
Cracks in the mirror hypothesis: high specularity does not reduce detection or predation risk
Open the record for dataset details and reuse information.
Code for individual-based simulations in "Environmental fluctuations can promote evolutionary rescue in high-extinction-risk scenarios"
<p>Substantial environmental change can force a population onto a path towards extinction, but under some conditions, adaptation by natural selection can rescue the population and allow it to persist. This process, known as evolutionary rescue, is believed to be less likely to occur with greater magnitudes of random environmental fluctuations because environmental variation decreases expected population size, increases variance in population size, and increases evolutionary lag. However, previous studies of evolutionary rescue in fluctuating environments have only considered scenarios in which evolutionary rescue was likely to occur. We extend these studies to assess how baseline extinction risk (which we manipulated via changes in the initial population size, degree of environmental change, or mutation rate) influences the effects of environmental variation on evolutionary rescue following an abrupt environmental change. Using a combination of analytical models and stochastic simulations, we show that autocorrelated environmental variation hinders evolutionary rescue in low-extinction-risk scenarios but facilitates rescue in high-risk scenarios. In these high-risk cases, the chance of a run of good years counteracts the otherwise negative effects of environmental variation on evolutionary demography. These findings can inform the development of effective conservation practices that consider evolutionary responses to abrupt environmental changes.</p>
High elevation increases the risk of Y chromosome loss in Alpine skink populations with sex reversal
<p>The view genotypic sex determination (GSD) and environmental sex determination (ESD) are mutually exclusive states has been contradicted by the discovery that chromosomal sex and environmental influences can co-exist within the same species, hinting at a continuum of intermediate states. Systems where genes and the environment interact to determine sex present the opportunity for sex reversal to occur, where the phenotypic sex is the opposite of that predicted by their sex chromosome complement. The skink Bassiana duperreyi has XX:XY sex chromosomes with sex reversal of the XX genotype to a male phenotype in response to exposure to cold incubation temperatures. Here we studied the frequency of sex reversal in B. duperreyi in response to climatic variation, using elevation as a surrogate for environmental temperatures. We demonstrate sex reversal for the first time in free-ranging adults of a reptile species with XX/XY sex determination. The highest frequency of sex reversal occurred at the highest elevation location, Mount Ginini (18.64%) and decreases in frequency with elevation. We model the impact of this under Fisher's frequency dependent selection to show that, only at the highest elevations, populations risk the loss of the Y chromosome and a transition to TSD. This study contributes to our understanding of the risks of extinction from climate change in species subject to sex reversal by temperature, and will provide focus for future research to test on-the-ground management strategies to mitigate the effects of climate in local populations.</p> <div> <div> <div class="msocomtxt"> <p class="MsoCommentText"> </p> </div> </div> </div>
Longitudinal proteomic profiling of high-risk patients with COVID-19 reveals markers of severity and predictors of fatal disease
<p>End-stage kidney disease (ESKD) patients are at high risk of severe COVID-19. We performed dense serial blood sampling in hospitalised and non-hospitalised ESKD patients with COVID-19 (n=256 samples from 55 patients) and used Olink immunoassays to measure 436 circulating proteins. Comparison to 51 non-infected ESKD patients revealed 221 proteins differentially expressed in COVID-19, of which 69.7% replicated in an independent cohort of 46 COVID-19 patients. 203 proteins were associated with clinical severity scores, including IL6, markers of monocyte recruitment (e.g. CCL2, CCL7), neutrophil activation (e.g proteinase-3) and epithelial injury (e.g. KRT19). Random Forests machine learning identified predictors of current or future severity such as KRT19, PARP1, PADI2, CCL7, and IL1RL1 (ST2). Survival analysis with joint models revealed 69 predictors of death including IL22RA1, CCL28, and the neutrophil-derived chemotaxin AZU1 (Azurocidin). Finally, longitudinal modelling with linear mixed models uncovered 32 proteins that display different temporal profiles in severe versus non-severe disease, including integrins and adhesion molecules. Our findings point to aberrant innate immune activation and leucocyte-endothelial interactions as central to the pathology of severe COVID-19. The data from this unique cohort of high-risk individuals provide a valuable resource for identifying drug targets in COVID-19.</p>
Forest gaps around wind turbines attract bat species with high collision risk
<p><span>Globally, renewable energy is highly demanded, leading to a recent increase in the number of wind turbines at forested sites. For the deployment of turbines, forest areas must be cleared, which results in significant habitat changes. To assess the ecological consequences of these changes for forest-associated bats, we quantified the activity of three bat foraging guilds at turbine clearings, adjacent forest edges, and nearby forest canopies. Specifically, open-space and edge-space foraging bats were more active at turbine clearings and forest edges than at forest canopies. Narrow-space foragers were also more often recorded at turbine clearings than at forest canopies. An increased activity of open- and edge-space foragers at turbine clearings may increase the risk for casualties. </span><span>Therefore, if turbines need to be placed in forests, strict curtailment schemes should be practiced to mitigate collision risk for these bats. This may impair the efficacy of wind energy production at forested sites.</span></p>
Mangroves as nature-based mitigation for ENSO-driven compound flood risks in a large river delta: supporting data - high water levels
<p>This dataset contains modelled high water levels in the Guayas delta supporting the paper 'Mangroves as nature-based mitigation for ENSO-driven compound flood risks in a large river delta' published in HESS 2024.</p> <p>The dataset is organised through two folders:</p> <ul> <li>mangroves: all data from the scenarios with mangroves included in the domain</li> <li>no_mangroves: all data from the scenarios without mangroves included in the domain</li> </ul> <p>Each folder is further divided along 6 subfolders:</p> <ul> <li>I: El Niño Ocean & river</li> <li>II: El Niño Ocean</li> <li>III: El Niño river</li> <li>IV: Neutral</li> <li>I_50per: 50 % increase in seaward El Niño anomalies</li> <li>I_150per: 150 % increase in seaward El Niño anomalies</li> </ul> <p>Each folder contains two files:</p> <ul> <li>vars.csv - each row represents a mesh node and there are three columns: <ul> <li>X: x value of the model mesh node [m]</li> <li>Y: y value of the model mesh node [m]</li> <li>HIGH_WATER: high water level [m]</li> </ul> </li> </ul>
Chromosomal instability degrades developmental phenotypes essential for anti-GD2 immunotherapy outcomes in high-risk neuroblastoma
<p>Childhood Cancer Data Initiative (CCDI)<br>dbGaP Study Accession: phs002431</p>
Not all regions with high pesticide risk deserve priority concern
<p>The datasets with 14 sheets contain basic data on pesticide use in China since 1991, parameters of four widely used pesticides (carbofuran, chlorpyrifos, atrazine and acetochlor), and related changing legacies, concentrations, and ecological risk in multimedia of each basin for 30 years. The detailed content can be found in the sheet 'Readme'.</p>
Hormone receptors AR, ER, PR and growth factor receptor Her-2 expression in oral squamous cell carcinoma: Correlation with overall survival, disease-free survival and 10-year survival in a high-risk population
<p>Oral squamous cell carcinoma (OSCC) comprises most of head and neck neoplasms and is one of the highest-ranking and lethal cancers in Pakistan due to prevailing mouth habits. Growth and hormonal receptors act as prognostic markers and targets for therapy in some cancers, but their application in OSCC is largely unexplored. This study aimed to evaluate the expression of growth and hormonal receptors in OSCC patients and correlate it with 10-year, overall and disease-free survival. To achieve this objective, immunohistochemistry for Her-2, AR, ER and PR was performed on 100 formalin-fixed paraffin-embedded primary OSCC specimens. Receptor expression was correlated with mouth habits and clinicopathological features and patient survival was analyzed using Kaplan-Meier method and Cox regression univariate analysis. We observed that in 100 patients, there were 57 males and 43 females. Immunopositive Her-2 expression was observed in 21% of patients, AR in 13%, ER in 3% and 0% for PR. Patients with betel quid/areca nut mouth habits had significantly absent Her-2 expression (P=0.035). Also, Her-2 negative patients were also negative for AR expression (P=0.002). Her-2 positive patients had poor 10-year survival (P=0.041). A trend of low survival and high recurrence rate was observed in AR positive patients, but this was not significant (P=0.072). No statistically relevant correlations were seen in the case of ER and PR. In conclusion, Her-2 may be a valuable marker for predicting long-term prognosis of OSCC patients.</p>
Multiple-batch spawning: a risk spreading strategy disarmed by highly intensive size-selective fishing
<p>Here we upload the files that support our research on the role of risk-spreading strategies in the light of fisheries-induced evolution. The code is stored in Zenodo.</p> <p><strong>Abstract from the paper:</strong></p> <p>Can the advantage of risk-managing life-history strategies become a disadvantage under human-induced evolution? Organisms have adapted to the variability and the uncertainty of environmental conditions with a vast diversity of life-history strategies. One of such evolved strategies is multiple-batch spawning, a spawning strategy common to long-lived fishes that 'hedge their bets', by distributing the risk to their offspring on a temporal and spatial scale. The fitness benefits of this spawning strategy increase with female body size, the very trait that size-selective fishing targets. By applying an empirically and theoretically motivated eco-evolutionary mechanistic model that was parameterized for Atlantic cod (<em>Gadus morhua</em>), we explored how fishing intensity may alter the life-history traits and fitness of fishes that are multiple-batch spawners. Our main findings are twofold; first, the risk-spreading strategy of multiple-batch spawning is not effective against fisheries selection, because the fisheries selection favours smaller fish with lower risk-spreading effect, and second, the ecological recovery in population size does not secure evolutionary recovery in the population size structure. The beneficial risk-spreading mechanism of the batch spawning strategy highlights the importance of recovery in the size structure of overfished stocks, from which a full recovery in the population size can follow.</p>
Data from: High predation risk decimates survival during the reproduction season
<p>Predators attack conspicuous prey phenotypes that are present in the environment. Male display behaviour of conspicuous nuptial colouration becomes risky in the presence of a predator, and adult males face higher predation risk. High predation risk in one sex will lead to low survival and sex ratio bias in adult cohorts, unless the increased predation risk is compensated by higher escape rate. </p> <p>Here, we tested the hypothesis that sand lizards (<em>Lacerta</em> <em>agilis</em>) have sex-specific predation risk and escape rate. We expected the differences to manifest in changes in sex ratio with age, differences in frequency of tail autotomy, and in sex-specific survival rate.</p> <p>We developed a statistical model to estimate predation risk and escape rate, combining the observed sex ratio and frequency of tail autotomy with likelihood-based survival rate. Using a Bayesian framework, we estimated the model parameters. We projected the date of the tail autotomy events from growth rates derived from capture-recapture data measurements.</p> <p>We found statistically stable sex ratio in age groups, equal frequency of tail regenerates between sexes, and similar survival rate. Predation risk is similar between sexes, and escape rate increases survival by about 5%. We found low survival rate and a low number of tail autotomy events in females during months when sand lizards mate and lay eggs, indicating high predator pressure throughout reproduction. Our data show that gravid females fail to escape predation. </p> <p>The risks of reproduction season in an ectotherm are a convolution of morphological changes (conspicuous colouration in males, body allometry changes in gravid females), behaviour (nuptial displays), and environmental conditions which challenge lizard thermal performance. Performance of endotherm predators in cold spring months endangers gravid females more than displaying males in bright nuptial colouration. </p>
Adaptation required to preserve future high-end river flood risk at present levels
<p>Dataset accompanying the publication</p> <p>S.N. Willner, A. Levermann, F. Zhao, K. Frieler, Adaptation required to preserve future high-end river flood risk at present levels. Sci. Adv. 4, eaao1914 (2018).</p> <p>The dataset includes the increase in flood protection that is required to keep the observed high-end flood risk of the past constant in the next 25 years as well as the affected population in both periods used (1971-2004 and 2035-2044).</p>
Fig. 1 in Circulating dengue virus serotypes and vertical transmission in AEdES larvae during outbreak and inter-outbreak seasons in a high dengue risk area of Sri Lanka
Fig. 1 Map of Sri Lanka showing the location of Mawanella, the study area
Table 2 in Circulating dengue virus serotypes and vertical transmission in AEdES larvae during outbreak and inter-outbreak seasons in a high dengue risk area of Sri Lanka
<p><b>Table 2</b> Distribution of DENV serotypes in patients with suspected dengue and in <i>Aedes</i> mosquito larvae</p><table><tbody><tr><th>Patient no.</th><th><i>Ae. aegypti</i></th><th><i>Ae. albopictus</i></th><th>DENV serotype identified in mosquito pools</th><th>DENV serotype identified in patients</th></tr></tbody><tbody><tr><th>1</th><td>Detected</td><td>ND</td><td>DENV-3</td><td>DENV-3</td></tr><tr><th>2</th><td>ND</td><td>Detected</td><td>DENV-1</td><td>DENV-1</td></tr><tr><th>3</th><td>ND</td><td>Detected</td><td>DENV-3</td><td>DENV-3</td></tr><tr><th>4</th><td>ND</td><td>Detected</td><td>DENV-4</td><td>ND</td></tr><tr><th>5</th><td>ND</td><td>Detected</td><td>DENV-3</td><td>ND</td></tr><tr><th>6</th><td>ND</td><td>Detected</td><td>DENV-1</td><td>ND</td></tr><tr><th>7</th><td>Detected</td><td>ND</td><td>DENV-2</td><td>ND</td></tr><tr><th>8</th><td>Detected</td><td>ND</td><td>DENV-1</td><td>ND</td></tr><tr><th>9</th><td>Detected</td><td>ND</td><td>DENV-1</td><td>ND</td></tr><tr><th>10</th><td>ND</td><td>Detected</td><td>DENV-3</td><td>ND</td></tr><tr><th>11</th><td>ND</td><td>Detected</td><td>DENV-2</td><td>ND</td></tr><tr><th>12</th><td>ND</td><td>Detected</td><td>DENV-2</td><td>DENV-1</td></tr><tr><th>13</th><td>ND</td><td>Detected</td><td>DENV-2</td><td>ND</td></tr><tr><th>14</th><td>ND</td><td>Detected</td><td>DENV-4</td><td>ND</td></tr><tr><th>15</th><td>ND</td><td>Detected</td><td>DENV-1</td><td>ND</td></tr><tr><th>16</th><td>ND</td><td>Detected</td><td>DENV-2</td><td>DENV-2</td></tr></tbody></table><p><i>ND</i> Not detected</p>
Table 1 in Circulating dengue virus serotypes and vertical transmission in AEdES larvae during outbreak and inter-outbreak seasons in a high dengue risk area of Sri Lanka
<p><b>Table 1</b> Distribution of <i>Aedes</i> mosquito larvae in and around residences of patients with suspected dengue in Mawanella from December 2015 to March 2017</p><table><tbody><tr><th>Period</th><th>Month and year of sample collection</th><th>Total no. of vector pools collected in entomological survey</th><th>No. of <i>Aedes</i> mosquito pools identified</th></tr><tr><th><i>Ae. aegypti</i></th><th><i>Ae. albopictus</i></th></tr></tbody><tbody><tr><th>Epidemic</th><td>12/2015</td><td>18</td><td>3</td><td>15</td></tr><tr><th></th><td>1/2016</td><td>22</td><td>8</td><td>14</td></tr><tr><th>Inter-epidemic</th><td>2/2016</td><td>5</td><td>0</td><td>5</td></tr><tr><th></th><td>3/2016</td><td>3</td><td>1</td><td>2</td></tr><tr><th></th><td>4/2016</td><td>4</td><td>1</td><td>3</td></tr><tr><th></th><td>5/2016</td><td>12</td><td>1</td><td>11</td></tr><tr><th></th><td>6/2016</td><td>15</td><td>9</td><td>6</td></tr><tr><th>Epidemic</th><td>7/2016</td><td>7</td><td>1</td><td>6</td></tr><tr><th></th><td>8/2016</td><td>5</td><td>2</td><td>3</td></tr><tr><th></th><td>9/2016</td><td>5</td><td>2</td><td>3</td></tr><tr><th>Inter-epidemic</th><td>10/2016</td><td>6</td><td>1</td><td>5</td></tr><tr><th></th><td>11/2016</td><td>6</td><td>1</td><td>5</td></tr><tr><th>Epidemic</th><td>12/2016</td><td>14</td><td>3</td><td>11</td></tr><tr><th></th><td>1/2017</td><td>23</td><td>8</td><td>15</td></tr><tr><th>Inter-epidemic</th><td>2/2017</td><td>1</td><td>0</td><td>1</td></tr><tr><th></th><td>3/2017</td><td>25</td><td>8</td><td>17</td></tr><tr><th>Total</th><td></td><td>171</td><td>49</td><td>122</td></tr></tbody></table>
Dataset for "Dissociable Roles of the mPFC-to-VTA pathway in the control od Impulsive action and Risk-Related Decision-Making in Roman High- and Low-Avoidance Rats"
<p>This dataset corresponds to the study "Dissociable Roles of the mPFC-to-VTA Pathway in the Control of Impulsive Action and Risk-Related Decision-Making in Roman High- and Low-Avoidance Rats". In this study, we used Positron Emission Tomography with [18F]-Fluorodeoxyglucose to evaluate brain metabolic activity in Roman High- (RHA) and Low-avoidance (RLA) rats, which exhibit innate differences in impulsivity. Notably, we used a viral-based intersectional chemogenetic strategy to isolate the role of the mPFC-to-VTA pathway in controlling impulsive behaviors. We selectively activated the mPFC-to-VTA pathway in RHA rats and inhibited it in RLA rats, assessing the effects on impulsive action and RDM in the rat gambling task. Our results showed that RHA rats displayed higher impulsive action, less optimal decision-making, and lower cortical activity than RLA rats at baseline. Chemogenetic activation of the mPFC-to-VTA pathway reduced impulsive action in RHA rats, whereas chemogenetic inhibition had the opposite effect in RLA rats. However, these manipulations did not affect RDM. Our findings suggest a dissociable role of the mPFC-to-VTA pathway in impulsive action and RDM, highlighting its potential as a target for investigating impulsivity-related disorders.</p> <p><strong>Contributions for usage of this data in publications:</strong></p> <p>If you publish any work using these data, please cite this repository and the associated publication.</p>
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.
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.
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.
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.
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.