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Dataset results
599 results for “Volatile”
Gene expression profiles of human promyelocytic leukemia cell lines exposed to six volatile organic compounds
GEO Series GSE12353. Homo sapiens. 27 samples. Type: Expression profiling by array.
Expression data from volatile treated and insect damaged Arabidopsis thaliana
GEO Series GSE33505. Arabidopsis thaliana. 16 samples. Type: Expression profiling by array.
To a better understanding of the impact of vine nitrogen status on volatile thiols from plot to transcriptome level
GEO Series GSE77895. Vitis vinifera. 24 samples. Type: Expression profiling by high throughput sequencing.
Volatiles of two growth-inhibiting rhizobacteria commonly enroll AtWRKY18 function
GEO Series GSE35325. Arabidopsis thaliana. 20 samples. Type: Expression profiling by array.
Volatile metabolome and floral transcriptome analyses reveal the volatile components of strongly fragrant progeny of Malus robusta Rehder
GEO Series GSE216719. Malus x robusta. 27 samples. Type: Expression profiling by high throughput sequencing.
Priming defense genes and metabolites in hybrid poplar by the green leaf volatile cis-3-hexenyl acetate
GEO Series GSE11955. Populus x canadensis; Populus tremuloides. 8 samples. Type: Expression profiling by array.
Reactive leaf volatiles act as powerful inducers of abiotic stress-related gene expression [NimbleGen]
GEO Series GSE64355. Arabidopsis thaliana. 4 samples. Type: Expression profiling by array.
Cellular reactions to long-term volatile organic compound (VOC) exposures.
GEO Series GSE76790. Homo sapiens. 18 samples. Type: Expression profiling by array.
Antifungal mechanism of volatile compounds emitted by Actinomycetota Paenarthrobacter ureafaciens from a disease-suppressive soil on Saccharomyces cerevisiae.
GEO Series GSE240052. Saccharomyces cerevisiae. 6 samples. Type: Expression profiling by high throughput sequencing.
Honey bee foraging decisions are influenced by pear flower volatiles
<p>Data of honey bee foraging bias on pear flowers.</p>
Fig. 2 in Variation in the amino acids, volatile organic compounds and terpenes profiles in induced polyploids and in Solanum tuberosum varieties
Fig. 2. Biplot of Principal Component Analysis based on VOCs and Amino acids from leaves of Solanum allotetraploids (a), autotetraploids (b) and cultivated varieties (c). Components were calculated using Euclidean distances. Amino acids are depicted in the three-letter code. a) Allotetraploids (4xAL2 and 4xAL4) and diploid S. tuberosum x S. kurtzianum parental interspecific hybrid (2xPIH). b) Autotetraploids (4xAuL1, 4xAuL2 and 4xAuL3) and diploid S. kurtzianum parental line (2xPL). c) S. tuberosum cultivated varieties (4xCalen, 4xInnovator and 4xPampeana).
Fig. 1 in Identification of herbivore-induced plant volatiles from selected Rubus species fed upon by raspberry bud moth (Heterocrossa rubophaga) larvae
Fig. 1. Preliminary analysis of host plant headspace by functional group and normalized total ion count (TIC).
Fig. 2 in Identification of herbivore-induced plant volatiles from selected Rubus species fed upon by raspberry bud moth (Heterocrossa rubophaga) larvae
Fig. 2. Mass spectra of unknown nitrogenous compounds from Rubus fruticosus (blackberry) and Rubus ursinus var. loganobaccus cv Boysenberry (Boysenberry) plants fed upon by Heterocrossa rubophaga larvae.
Fig. 2 in Volatile metabolic profiling and functional characterization of four terpene synthases reveal terpenoid diversity in different tissues of Chrysanthemum indicum L
Fig. 2. Content (percentages) of monoterpenoids and sesquiterpenoids in different tissues of C. indicum. (A) Monoterpenoid and sesquiterpenoid content in the different tissues. (B) Monoterpenoids and sesquiterpenoids in the root and flower bud of C. indicum.
Fig. 7 in Relative contribution of LOX10, green leaf volatiles and JA to woundinduced local and systemic oxylipin and hormone signature in Zea mays (maize)
Fig. 7. Levels of JAs (A) and some non-oxylipin metabolites (B) in leaves of WT (blue squares), lox10 (red circles) and opr7opr8 (green triangles) after wounding treatment. Values are mean ± standard error (n ≥ 4). Statistical differences are presented in Supplemental Fig. S2.
Fig. 3 in Relative contribution of LOX10, green leaf volatiles and JA to woundinduced local and systemic oxylipin and hormone signature in Zea mays (maize)
Fig. 3. Basal levels of oxylipins in roots of WT, lox10 and opr7opr8. (A) 9-LOX-derived products; (B), (C) and (D) 13-LOX-derived products; (E) α-DOX-derived 2-HOD and 10-HOD generated by reactive oxygen species (ROS). Values are mean ± standard error (n = 5). Different letters show significant differences (one-way ANOVA, S–N–K, P <0.05).
Fig. 4. 9 in Relative contribution of LOX10, green leaf volatiles and JA to woundinduced local and systemic oxylipin and hormone signature in Zea mays (maize)
Fig. 4. 9-LOX-derived oxylipin accumulation in leaves of WT (blue squares), lox10 (red circles) and opr7opr8 (green triangles) after wounding treatment. Values are mean ± standard error (n ≥ 4). Statistical differences are presented in Supplemental Fig. S2.
Fig. 1 in Effect of Monochamus galloprovincialis feeding on Pinus pinaster and Pinus pinea, oleoresin and insect volatiles
Fig. 1. Changes in the profile of volatiles released by all Pinus pinaster trees being fed on by Monochamus galloprovincialis adults. Bars: standard error. Letters in the table on the right side of the graph represent ANOVA post-hoc Fisher's Least Significant Difference test Homogenous Groups; (1) ANOVA with all volatiles: F(16,629) = 4.07; p <0.0001***; (2) ANOVA without α-pinene and β-pinene: F(14,555) = 4.63; p
AUGMENTED RESPONSE OF VOLATILE BIOMARKERS IN THE ASSESSMENT OF OESOPHAGOGASTRIC CANCER (AROMA2)
ClinicalTrials.gov study NCT07260734. IPD Sharing: NO. Countries: 0. Publications: 0.
A Clinical Study on the Effects of Inhalation of Volatile Oil of Cang-Ai Via the Nose on Patients With Depression
ClinicalTrials.gov study NCT05251779. IPD Sharing: YES. Countries: 0. Publications: 0.
ScienceDex guides
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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.