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986 results for “exchange”
Fig. 8 in Rosmarinic acid and hesperidin regulate gas exchange, chlorophyll fluorescence, antioxidant system and the fatty acid biosynthesis-related gene expression in Arabidopsis thaliana under heat stress
Fig. 8. The changes of the relative expression of WRI1 (A), BCCP2 (B), FAD2 (C), FAD3 (D) genes encoding after rosmarinic acid (RA, 100 μM) and/or hesperidin (HP, 100 μM) with/without heat stress (38 ◦C) in A. thaliana leaves. Multivariate data analyses of gene expression analysis under investigation.
Fig. 5 in Rosmarinic acid and hesperidin regulate gas exchange, chlorophyll fluorescence, antioxidant system and the fatty acid biosynthesis-related gene expression in Arabidopsis thaliana under heat stress
Fig. 5. The changes of the relative band intensity of different types of glutathione S-transferase activity isoenzymes (GST, A) and GST activity (B), and glutathione peroxidase activity (GPX, C) after rosmarinic acid (RA, 100 μM) and/or hesperidin (HP, 100 μM) with/without heat stress (38 ◦C) in A. thaliana leaves.
Fig. 1 in Rosmarinic acid and hesperidin regulate gas exchange, chlorophyll fluorescence, antioxidant system and the fatty acid biosynthesis-related gene expression in Arabidopsis thaliana under heat stress
Fig. 1. The average absorption per active reaction center (ABS/RC), the electron transport flux per active reaction center (ETo/RC), the flux of trapped exciton per active reaction center (TRo/RC), and the energy flow on the acceptor side of PSI ((Ro), The number of QA-reducing reaction centers per PSII antenna chlorophyll ((ΦPo/(1-ΦPo)), the efficiency with which a trapped exciton transfers an electron to the photosynthetic electron transfer chain ((ΨEo/(1-ΨEo)), the number of QA- reducing reaction centers per PSII antenna chlorophyll (γRC/(1-γRC)), the ratio of total dissipation to the number of active reaction centers (DIo/RC). The relative variable fluorescence intensity at J (VJ) and I step (VI), the performance index based on light absorption (PIABS), and the performance index (potential) for energy conservation from exciton to PSI and acceptor reduction (PItotal) were determined in A. thaliana leaves following treatment with rosmarinic acid (RA, 100 μM) and/or hesperidin (HP, 100 μM) with/without heat stress (38 ◦ C).
Fig. 7 in Rosmarinic acid and hesperidin regulate gas exchange, chlorophyll fluorescence, antioxidant system and the fatty acid biosynthesis-related gene expression in Arabidopsis thaliana under heat stress
Fig. 7. The changes of monodehydroascorbate reductase activity (MDHAR, A), dehydroascorbate reductase activity (DHAR, B), ascorbate content (AsA, C), dehydroascorbate content (DHA, D), glutathione content (GSH, E), oxidized glutathione content (GSSG, F), AsA/DHA (G), GSH/GSSG (H) and GSH redox state (I) after rosmarinic acid (RA, 100 μM) and/or hesperidin (HP, 100 μM) with/without heat stress (38 ◦C) in A. thaliana leaves.
Fig. 4 in Rosmarinic acid and hesperidin regulate gas exchange, chlorophyll fluorescence, antioxidant system and the fatty acid biosynthesis-related gene expression in Arabidopsis thaliana under heat stress
Fig. 4. The changes of the relative band intensity of different types of peroxidase isoenzymes (POX, A) and POX activity (B), relative band intensity of different types of NADPH oxidase isoenzymes (NOX, C) and NOX activity (D) after rosmarinic acid (RA, 100 μM) and/or hesperidin (HP, 100 μM) with/without heat stress (38 ◦C) in A. thaliana leaves.
Fig. 3 in Rosmarinic acid and hesperidin regulate gas exchange, chlorophyll fluorescence, antioxidant system and the fatty acid biosynthesis-related gene expression in Arabidopsis thaliana under heat stress
Fig. 3. The changes of the relative band intensity of different types of superoxide dismutase isoenzymes (SOD, A) and SOD activity (B), the relative band intensity of different types of catalase isoenzymes (CAT, C) and CAT activity (D) after rosmarinic acid (RA, 100 μM) and/or hesperidin (HP, 100 μM) with/without heat stress (38 ◦C) in A. thaliana leaves.
Fig. 2 in Rosmarinic acid and hesperidin regulate gas exchange, chlorophyll fluorescence, antioxidant system and the fatty acid biosynthesis-related gene expression in Arabidopsis thaliana under heat stress
Fig. 2. The changes of hydrogen peroxide content (H O, A), lipid peroxidation (TBARS content, B), histochemical staining for O • accumulation (C), histochemical 2 2 2 staining for H2O2 determination (D), histochemical staining for plasma membrane integrity (E) and histochemical staining for lipid peroxidation (F) after rosmarinic acid (RA, 100 μM) and/or hesperidin (HP, 100 μM) with/without heat stress (38 ◦C) in A. thaliana leaves.
Fig. 6 in Rosmarinic acid and hesperidin regulate gas exchange, chlorophyll fluorescence, antioxidant system and the fatty acid biosynthesis-related gene expression in Arabidopsis thaliana under heat stress
Fig. 6. The changes of the relative band intensity of different types of ascorbate glutathione isoenzymes (APX, A) and APX activity (B), and glutathione reductase activity (GR, C) after rosmarinic acid (RA, 100 μM) and/or hesperidin (HP, 100 μM) with/without heat stress (38 ◦C) in A. thaliana leaves.
Landscapes of exchange in the Willaumez Peninsula, West New Britain, Papua New Guinea (Dataset)
<p>The tables presented here contain the complete set of data used to construct the summary Tables and Figures presented in the chapter ‘Landscapes of exchange in the Willaumez Peninsula, West New Britain, Papua New Guinea’ by Gustavo F. Bonnat, Robin Torrence and Peter White which is published inthe book titled 40 Years in the South Seas: Archaeological Perspectives on the Human History of Papua New Guinea and the Western Pacific, edited by A. Ford, B. Shaw, D. Gaffney and published by ANU Press, Canberra.</p>
The story of Knowledge exchange
<p>Knowledge exchange in the International Monetary Fund</p>
Electrodialysis with Bipolar Membranes for the Generation of NaOH and HCl Solutions from Brines: An Inter-Laboratory Evaluation of Thin and Ultrathin Non-Woven Cloth-Based Ion-Exchange Membranes
<p>The SEArcularMINE project aims to recover critical raw materials (CRMs) from brines from saltworks, thus facing a CRM shortage within Europe. To promote a fully circular scheme, the project valorises concentrated brines using electrodialysis with bipolar membranes (EDBM) to generate the required amounts of reactants (i.e., acids and bases). Regarding the performances of new non-woven cloth ion-exchange membranes (Suez): (i) an ultra-thin non-woven polyester cloth and (ii) a thin polypropylene cloth acting as the support structures were assessed. Additionally, the anion layer includes a catalyst to promote the water dissociation reaction. The effect of current density (100, 200, and 300 Am−2) on the performance of two combinations of membranes in an inter-laboratory exercise using 2 M NaCl was evaluated. According to statistical analysis ANOVA, there was an agreement on the results obtained in both laboratories. NaOH/HCl solutions up to 0.8 M were generated working at 300 A m−2 using both combinations of membranes. Regarding the performance parameters, stack set-ups incorporating thin polypropylene membranes showed lower specific energy consumption (SEC) and higher specific productivity (SP) than ultra-thin polypropylene ones. Hence, for ultra-thin polypropylene membranes, SEC was reported to be between 2.18 and 1.69 kWh kg−1 NaOH and SP between 974 and 314 kg m−2 y−1.<br> </p>
Pre-Workshop Survey Report | 21-22 April 2023 OA Book Usage Data Exchange and Use Guidelines and Principles Meeting
<p>This document contains anonymous data collected through two pre-event surveys of invited event participants. The file was shared with and discussed among participants at the 21-22 April 2023 OA Book Usage Data Exchange and Use Guidelines and Principles Meeting. </p>
Dataset for paper "Equatorial Pacific sea-air CO2 exchange modulated by upper ocean circulation during the last deglaciation" submittted to Geophysical Research Letters
<p>Data of the <em>p</em>CO<sub>2</sub> and ∆<em>p</em>CO<sub>2_sw-atm</sub> from <em>G. ruber</em> 𝛿<sup>11</sup>B, 𝛿<sup>11</sup>B of <em>G. sacculifer</em>, 𝛿<sup>18</sup>O of <em>G. ruber</em> and <em>P. obliquiloculata</em>, ∆𝛿<sup>18</sup>O<sub>P-G</sub>, bulk 𝛿<sup>15</sup>N in core MD10-3340 (0º31.0’S, 128º43.5’E, water depth 1094 m), and upper Ocean Heat Content (OHC) in the Western Equatorial Pacific (WEP).</p>
Data for Dipolar spin-exchange and entanglement between molecules in an optical tweezer array
<p>Data for Dipolar spin-exchange and entanglement between molecules in an optical tweezer array</p>
Dynamic Phosphorus: Thiolate Exchange Cascades with Higher Phosphorothioates: Open data
<p>Original data underlying the publication entitled "Dynamic Phosphorus: Thiolate Exchange Cascades with Higher Phosphorothioates".</p><ol><li>Synthetic procedures and spectroscopic data of O[666], S[111], and S[666]</li><li>Dynamic exchange in organic solvent. Procedures and NMR data</li><li>DLS data and procedures</li><li>Dynamic exchange in micelles. Procedures and NMR data</li><li>Stability and exchange in water. Procedures and NMR and LC-MS data</li><li>Cell inhibition. Procedures, automatically analyzed data, and metadata</li></ol><p> </p>
Small Volume Plasma Exchange (SVPE) for Guillain-Barré Syndrome (GBS) Patients
ClinicalTrials.gov study NCT02780570. IPD Sharing: NO. Countries: 1. Publications: 3.
Characterization of Low Density Lipoprotein and Mechanism of the Pro Aggregant Effect Through Oxidant Stress and Lipid Exchange
ClinicalTrials.gov study NCT00932087. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Therapeutic Plasma Exchange in Resistant Cytokine Storm of COVID 19
ClinicalTrials.gov study NCT04457349. IPD Sharing: Not stated. Countries: 1. Publications: 13.
Reduce Patient Discomfort With Water Exchange Method During Upper Endoscopy
ClinicalTrials.gov study NCT04502485. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Comparison of the Cardiopulmonary and Gaz-exchange Response Between the Six-minute Stepper Test and the Incremental Cardiopulmonary Exercise Testing in Patients With Chronicle Obstructive Pulmonary Di
ClinicalTrials.gov study NCT04008615. IPD Sharing: Not stated. Countries: 1. Publications: 0.
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.