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122 results for “Dominance Effects”

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ClinicalTrials.gov36/100

Effect of Beetroot Juice on Reducing Hypertension in Autosomal Dominant Polycystic Kidney Disease

ClinicalTrials.gov study NCT05401409. IPD Sharing: Not stated. Countries: 1. Publications: 2.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov36/100

A Study to Evaluate the Effects of GLPG2737 in Participants With Autosomal Dominant Polycystic Kidney Disease (ADPKD)

ClinicalTrials.gov study NCT04578548. IPD Sharing: NO. Countries: 7. Publications: 1.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov36/100

Effect of Statin Therapy on Disease Progression in Autosomal Dominant Polycystic Kidney Disease (ADPKD)

ClinicalTrials.gov study NCT00456365. IPD Sharing: NO. Countries: 1. Publications: 7.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov36/100

Short-term Renal Hemodynamic Effects of Tolvaptan in Subjects With Autosomal Dominant Polycystic Kidney Disease (ADPKD)

ClinicalTrials.gov study NCT01336972. IPD Sharing: Not stated. Countries: 1. Publications: 5.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov36/100

Short-term Effects of an SGLT2 Inhibitor on Divalent Ions in Autosomal Dominant Polycystic Kidney Disease

ClinicalTrials.gov study NCT06435858. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
dryad36/100

The diverse effects of phenotypic dominance on hybrid fitness

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publicSep 2022View details →
dryad36/100

Evolution of wing shape in geometrid moths: phylogenetic effects dominate over ecology

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publicApr 2024View details →
dryad36/100

Short-term effects of continuous cover forestry on forest biomass production and biodiversity: Applying single-tree selection in forests dominated by Picea abies

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publicNov 2022View details →
dryad36/100

Integrated effects of neighborhood composition and resource levels on growth of a dominant tree species in a tropical forest

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publicJan 2025View details →
dryad36/100

Contrasting soil- and canopy-nurse effects on dependent species in metalliferous systems may be explained by dominant plant functional strategies

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publicNov 2022View details →
dryad36/100

On the biodiversity of diatom communities in lakes of east China: Geochemical effects dominated after eutrophication

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publicSep 2023View details →
dryad36/100

Data from: Forbs in Viking lands: The effect of disturbing dominant graminoids on recruitment in tundra grasslands

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publicOct 2025View details →
dryad36/100

Data from: Dominant species determine grazing effects on the stability of herbaceous community production at multiple scales in drylands

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publicJun 2023View details →
dryad36/100

Effects of dominant ant species on ant community structure and ant-hemipteran interactions

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publicAug 2023View details →
dryad36/100

Nitrogen enrichment drives accelerative effect of soil heterogeneity on the flowering phenology of a dominant grass

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publicDec 2024View details →
dryad36/100

Data from: Why are plant communities stable? Disentangling the role of dominance, asynchrony and averaging effect following realistic species loss scenario

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publicJun 2024View details →
dryad36/100

Data from: Tamm Review: a meta-analysis of thinning, prescribed fire, and wildfire effects on subsequent wildfire severity in conifer dominated forests of the Western US

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publicMay 2024View details →
dryad36/100

Data from: The functional effects of a dominant consumer are altered following the loss of a dominant producer

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publicAug 2023View details →
dryad32/100

Data from: The effect of competition on responses to drought and interannual climate variability of a dominant conifer tree of western North America

To accurately predict how ecosystems will respond to climate change – and how management actions can influence such responses – scientists and managers need a better understanding of how and when biotic interactions modify climate–growth relationships. However, current research has largely ignored the role of competition in modulating climate–growth relationships of mature trees. In this study, we assessed the effect of competition on tree responses to drought and interannual climate variability as well as linkages between climate sensitivity and morphological characteristics of the stem wood. We sampled 10 sites in north-eastern Washington, USA, and used dendroecology to quantify responses of Douglas-fir (Pseudotsuga menziesii) to drought and climate variability. Tree-ring series were converted to basal area increment series, and the effects of competition on climate–growth relationships were assessed at the tree and site levels using a combination of correlation analyses and linear mixed-effects models. Competition did not affect tree responses to extreme drought. When soil moisture was below average, tree growth was tightly coupled to climate variability for all trees, regardless of their competitive status. However, in wet years, competition had a pronounced, positive effect on climate sensitivity of growth. Trees with more competition from neighbours exhibited a significantly higher proportion of sapwood area in latewood (a morphological trait associated with greater drought resistance). Synthesis. Our results suggest that a tree's ability to cope with environmental variability is driven not just by the proximate effects of neighbours on resource availability, but also by phenotypic plasticity and long-term adaptations to competitive stress (such as changes in carbon allocation). Findings have important implications for individual-tree and stand-level growth models and may help managers better understand how their activities will modify tree responses to climate change.

opencc-zeroDec 2015View details →
dryad32/100

Data from: Stressor dominance and sensitivity-dependent antagonism: disentangling the freshwater effects of an insecticide among co-occuring agricultural stressors

1. Pesticide concentrations are correlated with regional declines in stream invertebrate diversity. Experimental studies have identified that pesticides can have strong and persistent negative effects on aquatic ecosystems. These effects may occur at concentrations orders of magnitude lower than laboratory toxicity studies predict. Synergism among stressors is one explanation for the observed laboratory-field difference. However, the true effect of pesticides on stream invertebrates remains uncertain, given interactions between stressors and natural environmental conditions. 2. We experimentally examined multiple-stressor effects on stream invertebrate assemblages and leaf-litter breakdown using 24 independent ~900 L re-circulating outdoor mesocosms in a semi-orthogonal design. Two pulses of the pesticide malathion (C10H19O6PS2) were delivered at low and high concentrations (Pulse 1: low at 0.1 and high at 1 µg L-1¬; Pulse 2: at 2.5 and 25 µg L-1). These were crossed with a treatment mimicking the combined stressors from agricultural development; nitrogen, phosphorus and clay (kaolin) sediment (hereafter agricultural stressors). 3. Malathion degradation was rapid (<24 hr half-life) in all treatments, likely because of photolysis, hydrolysis, the presence of biofilms and sorptive processes. There were significant differences in invertebrate assemblages between treatments, where malathion contributed to 48% and 87% of deviance during Pulse 1 and 2 respectively. Malathion had strong negative effects during Pulse 2, decreasing Ephemeroptera, Plecoptera and Trichoptera abundance (P<0.05), invertebrate richness (P<0.01) and total abundance (P<0.01). 4. Despite the dominant effects of malathion on invertebrates, agricultural stressors inhibited rates of leaf litter breakdown (P<0.05), increased invertebrate densities and weakly mitigated malathion toxicity in mesocosms (e.g. PERMANOVA, P≈0.1). Malathion breakdown analysis indicated sediment addition reduced malathion concentrations through alkaline hydrolysis and sorption. Experimental assays on common taxa indicated sediment was antagonistic with malathion. 5. Pesticide effects were not synergistic with the stressors tested here. Indeed, sensitivity-dependent stressor antagonisms were observed, reinforcing a mechanistic understanding of stressor effects and interactions is important. Among aquatic stressors examined, malathion had dominant effects on invertebrate assemblages, despite rapid degradation. Our results suggest that pesticide effects may be underestimated within ecosystems, where pesticides can have severe community wide effects, but rapid pesticide breakdown and sorptive processes may conceal causal links.01-May-2019

opencc-zeroMay 2019View 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