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19,468 results for “p”
Abb. P 11 in Dokumente zum wissenschaftlichen Opus von Ulrike Aspöck für die Periode 2011-2016 anlässlich ihres 75. Geburtstags
Abb. P 11: Publikationen von Ulrike Aspöck: 281 (2015), 282 (2015), 283 (2015).
Abb. P 10 in Dokumente zum wissenschaftlichen Opus von Ulrike Aspöck für die Periode 2011-2016 anlässlich ihres 75. Geburtstags
Abb. P 10: Publikationen von Ulrike Aspöck: 278 (2015), 279 (2015), 280 (2015).
Abb. P 9 in Dokumente zum wissenschaftlichen Opus von Ulrike Aspöck für die Periode 2011-2016 anlässlich ihres 75. Geburtstags
Abb. P 9: Publikationen von Ulrike Aspöck: 275 (2014), 276 (2014), 277 (2014).
Abb. P 13 in Dokumente zum wissenschaftlichen Opus von Ulrike Aspöck für die Periode 2011-2016 anlässlich ihres 75. Geburtstags
Abb. P 13: Publikationen von Ulrike Aspöck: 287 (2016).
Abb. P 7 in Dokumente zum wissenschaftlichen Opus von Ulrike Aspöck für die Periode 2011-2016 anlässlich ihres 75. Geburtstags
Abb. P 7: Publikationen von Ulrike Aspöck: 270 (2014), 271 (2014), 272 (2014).
Abb. P 8 in Dokumente zum wissenschaftlichen Opus von Ulrike Aspöck für die Periode 2011-2016 anlässlich ihres 75. Geburtstags
Abb. P 8: Publikationen von Ulrike Aspöck: 273 (2014), 274 (2014).
Abb. P 6 in Dokumente zum wissenschaftlichen Opus von Ulrike Aspöck für die Periode 2011-2016 anlässlich ihres 75. Geburtstags
Abb. P 6: Publikationen von Ulrike Aspöck: 267 (2014), 268 (2014), 269 (2014).
Abb. P 5 in Dokumente zum wissenschaftlichen Opus von Ulrike Aspöck für die Periode 2011-2016 anlässlich ihres 75. Geburtstags
Abb. P 5: Publikationen von Ulrike Aspöck: 264 (2013), 265 (2013), 266 (2014).
Abb. P 2 in Dokumente zum wissenschaftlichen Opus von Ulrike Aspöck für die Periode 2011-2016 anlässlich ihres 75. Geburtstags
Abb. P 2: Publikationen von Ulrike Aspöck: 254 (2012), 255 (2012), 256 (2012).
Abb. P 3 in Dokumente zum wissenschaftlichen Opus von Ulrike Aspöck für die Periode 2011-2016 anlässlich ihres 75. Geburtstags
Abb. P 3: Publikationen von Ulrike Aspöck: 257 (2012), 258 (2012), 259 (2013).
Abb. P 1 in Dokumente zum wissenschaftlichen Opus von Ulrike Aspöck für die Periode 2011-2016 anlässlich ihres 75. Geburtstags
Abb. P 1: Publikationen von Ulrike Aspöck: 251 (2012), 252 (2012), 253 (2012).
Abb. P 12 in Dokumente zum wissenschaftlichen Opus von Ulrike Aspöck für die Periode 2011-2016 anlässlich ihres 75. Geburtstags
Abb. P 12: Publikationen von Ulrike Aspöck: 284 (2016), 285 (2016), 286 (2016).
Fig. 3 in Orobanche rumseiana A. Pujadas & P. Fraga (Orobanchaceae), a new species from the Balearic Islands
Fig. 3. – Distribution of Orobanche rumseiana A. Pujadas & P. Fraga in Balearic Islands.
Raw recordings for electrophysiological characterization of CNO-DREADD mediated responses in noradrenergic locus coeruleus (LC) neurons from lines RR1(P), RR2(P), and RC::FPDi (P).
<p>Whole-cell recordings were performed as described previously by the Jiang lab. Briefly, patch pipettes (2-7 MΩ) were filled with an internal solution containing 120 mM potassium gluconate, 10 mM HEPES, 4 mM KCl, 4 mM MgATP, 0.3 mM Na<sub>3</sub>GTP, 10 mM sodium phosphocreatine and 0.5% biocytin (pH 7.25). Whole-cell recordings from up to 8 LC neurons were performed using two Quadro EPC 10 amplifiers (HEKA Electronic, Germany). PatchMaster (HEKA) and custom-written Matlab-based programs (Mathworks) were used to operate the recording system and perform online and offline data analysis. In current-clamp recordings, neurons were first current clamped at ~-40pA to prevent spontaneous firing. Prior to investigating the effect of drugs, we calculated spike thresholds and recorded firing patterns in response to sustained depolarizing currents by injecting increasing current steps (+10pA). Continuous recordings were obtained from LC neurons current clamped at -40 to 0 pA during drug wash-on experiments. We also calculated other intrinsic electrophysiological parameters, such as the input resistance, membrane time constant, spike amplitude, after-hyperpolarization (AHP) etc.</p>
Datasheet of Anti-Inflammatory Activity and Toxicity Evaluation of 1,3-bis(p-Hydroxyphenyl)urea
<p><strong>Background: </strong>Inflammation is a normal protective response caused by an injury or tissue damage, through physical trauma, damaging chemicals, or invasion of pathogenic microorganisms. One of the modified <em>p</em>-aminophenol compounds is 1,3-bis(<em>p</em>-hydroxyphenyl)urea, which was estimated to have more potent analgesic activity and fewer hepatotoxic side effects than paracetamol. When the lipophilicity of this compound increases between 1.8 to 4.4, it is observed to serve as an anti-inflammatory agent. Therefore, the determination of safety precaution is very necessary while testing for the toxicity effect of 1,3-bis(<em>p</em>-hydroxyphenyl)urea. This is due to the effectiveness and safety of suitable drugs.</p> <p><strong>Methods: </strong>An anti-inflammatory test was carried out by measuring the percentage of inflammation in rats, after the administration of 1,3-bis(<em>p</em>-hydroxyphenyl)urea was previously induced by the carrageenan solution intraplantar and the analysis of neutrophil values through a plethysmometer and Hematoxylin-Eosin method. Also, an acute toxicity test was performed by administering this p-aminophenol compound to female rats for 24 h and observed for 14 days. In addition, a subchronic toxicity test was conducted on male and female rats for 28 days, with continuous observations carried out for 42 days.</p> <p><strong>Results: </strong>The doses of 1,3-bis(<em>p</em>-hydroxyphenyl)urea at 50, 100, and 200 mg/Kg BW, had anti-inflammatory activity compared to diclofenac sodium at 2.25 mg/Kg BW. Also, there is no toxicity and animal death symptoms were observed in the acute and subchronic tests.</p> <p><strong>Conlclusion: </strong>This 1,3-bis(<em>p</em>-hydroxyphenyl)urea compound had an anti-inflammatory activity and relatively low toxicity.</p>
Datasheet of Anti-Inflammatory Activity and Toxicity Evaluation of 1,3 bis(p-Hydroxyphenyl)urea
<p><strong>Background: </strong>Inflammation is a normal protective response caused by an injury or tissue damage, through physical trauma, damaging chemicals, or invasion of pathogenic microorganisms. One of the modified p-aminophenol compounds is 1,3 bis (p-Hydroxyphenyl) urea, which was estimated to have more potent analgesic activity and fewer hepatotoxic side effects than paracetamol. When the lipophilicity of this compound increases between 1.8 to 4.4, it is observed to serve as an an- ti-inflammatory agent. Therefore, the determination of safety precaution is very necessary while testing for the toxicity effect of 1,3 bis (p-Hydroxyphenyl) urea. This is due to the effectiveness and safety of suitable drugs.</p> <p><strong>Methods: </strong>An anti-inflammatory test was carried out by measuring the per-centage of inflammation in rats, after the administration of 1,3 bis (p-Hydroxyphenyl) urea was previously induced by the carrageenan solution intraplantar and the analy- sis of neutrophil values through a plethysmometer and Hematoxylin-Eosin method. Also, an acute toxicity test was performed by administering this p-aminophenol com- pound to female rats for 24 h and observed for 14 days. In addition, a subchronic toxicity test was conducted on male and female rats for 28 days, with continuous observations carried out for 42 days.</p> <p><strong>Results:</strong>The doses of 1,3 bis (p-Hydroxyphenyl) urea at 50, 100, and 200 mg/Kg BW, had anti-inflammatory activity compared to diclofenac sodium at 2.25 mg/Kg BW. Also, there is no toxicity and animal death symp-toms were observed in the acute and subchronic tests.</p> <p><strong>Conlclusion:</strong>This p-aminophenol compound had an anti-inflammatory activity and relatively low toxicity.</p>
P-wave ocean site-effect maps
<p>P-wave ocean site-effect maps at 4-s and 5-s periods from Gualtieri et al. (2014).</p>
Data supporting "Can Long-Term Experiments Predict Real Field N and P Balance and System Sustainability? Results from Maize, Winter Wheat, and Soybean Trials Using Mineral and Organic Fertilisers"
<p>Data supporting "Can Long-Term Experiments Predict Real Field N and P Balance and System Sustainability? Results from Maize, Winter Wheat, and Soybean Trials Using Mineral and Organic Fertilisers" by Piccoli et al. (2021) Agronomy 2021, 11, 1472. https://doi.org/10.3390/agronomy11081472</p>
Author list of Anti-Inflammatory Activity and Toxicity Evaluation of 1,3-bis(p-Hydroxyphenyl)urea
<p><strong>Background: </strong>Inflammation is a normal protective response caused by an injury or tissue damage, through physical trauma, damaging chemicals, or invasion of pathogenic microorganisms. One of the modified <em>p</em>-aminophenol compounds is 1,3-bis(<em>p</em>-hydroxyphenyl)urea, which was estimated to have more potent analgesic activity and fewer hepatotoxic side effects than paracetamol. When the lipophilicity of this compound increases between 1.8 to 4.4, it is observed to serve as an anti-inflammatory agent. Therefore, the determination of safety precaution is very necessary while testing for the toxicity effect of 1,3-bis(<em>p</em>-hydroxyphenyl)urea. This is due to the effectiveness and safety of suitable drugs.</p> <p><strong>Methods: </strong>An anti-inflammatory test was carried out by measuring the percentage of inflammation in rats, after the administration of 1,3-bis(<em>p</em>-hydroxyphenyl)urea was previously induced by the carrageenan solution intraplantar and the analysis of neutrophil values through a plethysmometer and Hematoxylin-Eosin method. Also, an acute toxicity test was performed by administering this p-aminophenol compound to female rats for 24 h and observed for 14 days. In addition, a subchronic toxicity test was conducted on male and female rats for 28 days, with continuous observations carried out for 42 days.</p> <p><strong>Results: </strong>The doses of 1,3-bis(<em>p</em>-hydroxyphenyl)urea at 50, 100, and 200 mg/Kg BW, had anti-inflammatory activity compared to diclofenac sodium at 2.25 mg/Kg BW. Also, there is no toxicity and animal death symptoms were observed in the acute and subchronic tests.</p> <p><strong>Conlclusion: </strong>This 1,3-bis(<em>p</em>-hydroxyphenyl)urea compound had an anti-inflammatory activity and relatively low toxicity.</p>
Prediction and realisation of high mobility and degenerate p-type conductivity in CaCuP thin films Dataset
<p>Experimental and computational datasets for this publication, including README files. To unzip, in the command line paste the following command:</p> <blockquote> <p>tar -xzvf cacup_data_repository_v2.tar.gz</p> </blockquote> <p>And repeat the command:</p> <blockquote> <p>tar -xzvf <file.tar.gz></p> </blockquote> <p>for each necessary tar file.</p> <p>For any issues with accessibility, please email joe.willis.15@ucl.ac.uk.</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.