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334 results for “biological evaluation”
Dataset for "Evaluation of Publicly Available Information on Sex-related Differences in the Efficacy and Safety of New Molecular Entities and Therapeutic Biological Products"
<p>Contains our extraction sheets with additional documents/notes on methods used in our study.</p>
Ir and NMR for article Synthesis and Biological Activity Evaluation of New Isatin-Gallate Hybrids as Antioxidant and Anticancer Agents (in vitro) and In-silico Study as Anticancer Agents and Coronavirus Inhibitors
<p>this is IR and NMR data for article titled <strong>Synthesis and Biological Activity Evaluation of New Isatin-Gallate Hybrids as Antioxidant and Anticancer Agents (<em>in vitro</em>) and In-silico Study as Anticancer Agents and Coronavirus Inhibitors </strong></p> <p> </p>
Fig. 3 in Laboratory evaluations of the foraging success of Tamarixia radiata (Hymenoptera: Eulophidae) on flowers and extrafloral nectaries: potential use of nectar plants for conservation biological control of Asian citrus psyllid (Hemiptera: Liviidae)
Fig. 3. Choice of cups with either unscented sucrose solution or with bananascented sucrose solution made by Tamarixia radiata following a pre-test exposure to either 1.0 M sucrose solution or 1.0 M sucrose solution and banana flavor extract (G-test; ** = P ≤ 0.01; NS = not significant).
Fig. 1 in Laboratory evaluations of the foraging success of Tamarixia radiata (Hymenoptera: Eulophidae) on flowers and extrafloral nectaries: potential use of nectar plants for conservation biological control of Asian citrus psyllid (Hemiptera: Liviidae)
Fig. 1. Diagrammatic representation of nectary architectures presented to Tamarixia radiata in foraging evaluations. Location of nectaries shown in red. A. Cy- athium of euphorbiaceous species with exposed nectaries. B. Partially exposed nectaries as found in buckwheat. C. Partially hidden nectaries as found in alyssum. D. Partially exposed nectaries covered with trichomes as found in marjoram. E. Hidden nectaries as found in composites. Drawings are only indicative of size and spatial relationships and are not to scale.
Fig. 2 in Laboratory evaluations of the foraging success of Tamarixia radiata (Hymenoptera: Eulophidae) on flowers and extrafloral nectaries: potential use of nectar plants for conservation biological control of Asian citrus psyllid (Hemiptera: Liviidae)
Fig. 2. Mean (± SE) feeding time of Tamarixia radiata when presented with different concentrations of sugars commonly occurring in nectar (sucrose, fructose, glucose) and honeydew (melizitose, raffinose). Bars within the same concentration having different letters are different at P ≤ 0.05 (ANOVA).
Design, Synthesis and Biological Evaluation of 7-Chloro-9H-pyrimido[4,5-b]indole-based Glycogen synthase kinase-3β inhibitors
<p>The dataset related to the publication:</p> <p>Andreev et al. Design, Synthesis and Biological Evaluation of 7 Chloro-9H-pyrimido[4,5-b]indole-based Glycogen synthase kinase-3β inhibitors.<br> <br> The files include:</p> <p>1) Movies of the MD simulations of compounds 14b (<strong>Cmpd14b.mpg</strong>) and 24 (<strong>Cmpd24.mpg</strong>).</p> <p>2) Raw trajectory files of the Desmond MD simulations of the compounds 14b (<strong>14b.zip</strong>), 24 (<strong>24.zip</strong>) and 24 (3a<em>R</em>, 7a<em>S</em>) (<strong>24_3aR_7aS.zip</strong>) (contains out.cms and the full trj files).</p> <p>3) Output conformations of the QM Tautomer & Conformation Predictor of Maestro (Schrödinger, LLC, New York, NY, 2019) of the compounds<br> 14b (<strong>Cmpd14b_QMconftauto_output.mae</strong>; <strong>Cmpd14b_QMconftauto_output.sdf</strong>), <br> 24 (<strong>Cmpd24_QMconftauto_output.mae</strong>; <strong>Cmpd24_QMconftauto_output.sdf</strong>) and <br> 24 (3a<em>R</em>, 7a<em>S</em>) (<strong>Cmpd24_3aR_7aS_QMconftauto_output.mae</strong>; <strong>Cmpd24_3aR_7aS_QMconftauto_output.sdf</strong>)</p> <p>4) Jaguar pKa calculation (conformations) output-files for compounds 14b, 14c, 14d, 14e, 14f, 14g, 14h, 14i, 14j, 14k, 14l, 14m, 14n <strong>pKa.zip</strong> (contains conformation in .mae file and Final weighted pKa value in .out file).</p>
Figure 11 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 11. The efficacy of RM of orange peels against human pathogenic bacteria. ****Extremely significant among compared groups at p <0.05 level. Test 1: RM of Valen-cia orange; Test 2: RM of Mandarin orange; Test 3: RM of African navel orange.
Figure 6 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 6. The structure of bioactive compounds of RM of African Navel orange peel (1) Limonene; (2) Hexadecanoic acid, 2-hydroxy-1- (hydroxymethyl) ethyl; (3) 9,12-Octadecadienoic acid (Z,Z)-, methyl ester; (4) Terephthalic acid, di(2-ethylhexyl) ester; (5) α-Sitosterol; (6) α-D-Glucopyranose, 4-O-α-D-galactopyranosyl-; (7) 2-Methoxy-4-vinylphenol; (8) Eugenol; (9) cis-Vaccenic acid; (10) De-canal; (11) Vitamin E; (12) Dichloroxylenol.
Figure 3 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 3. GC-MS chromatogram of the RMs of orange peels. (A) RM of Valencia orange; (B) RM of Mandarin orange; (C) RM of African Navel orange.
Figure 2 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 2. The morphology of orange fruits. (A) Valenica orange; (B) Madarin orange; (C) African Navel orange.
Figure 5 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 5. The structure of bioactive compounds of RM of Mandarin orange peel (1) Lim-onene; (2) Octadecanoic acid, 2-hydroxy-1- (hydroxymethyl) ethyl; (3) Hexadecanoic acid, 2-hydroxy-1-(hydroxymethyl) ethyl; (4) Tetradecanamide; (5) n-Hexadecanoic acid; (6) α-D-Mannofuranoside, 1-O-(10-undecenyl)-; (7) 3-Deoxy-d-mannoic lactone; (8) Desulpho-sinigrin; (9) 2-Methoxy-4-vinylphenol; (10) Decanal; (11) Vitamin E; (12) 1-Monolinoleoylglycerol trimethylsilyl ether.
Figure 4 in Spectral characterization and biological evaluation of biomolecules from the peels of three orange fruits: a comparative study
Figure 4. The structure of bioactive compounds of RM of Valencia orange peel (1) Limonene; (2) 9-Octadecenamide, (Z)-; (3) Hexadecanoic acid, 2- hy-droxy-1-(hydroxymethyl)ethyl; (4) Octadecanoic acid, 2-hydroxy-1-(hydroxymethyl)ethyl; (5) Tetradecanamide; (6) Hexadecanamide; (7) Ethyl iso-allocholate; (8) Ethyl α-d-glucopyranoside; (9) d-Glycero-d-galacto-heptose; (10) α-Sitosterol; (11) Vitamin E; (12) 4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-5,6,7-trimethoxy-.
Synthesis and biological evaluation of a radiolabeled PET probe for visualization of in vivo -fucosidase expression - esi
<p>Supplementary data for paper titled: <strong>Synthesis and biological evaluation of a radiolabeled PET probe for visualization of <em>in vivo</em> </strong><strong>a</strong><strong>-fucosidase expression</strong></p>
Figures 53–58 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figures 53–58. Stereoscan photographs of Pimplinae. Figs 53, 54, mesopleuron; 53, Dolichomitus annulicornis; 54, Pimpla azteca. Figs 55–58, propodeum, dorsal; 55, Xanthopimpla aurita; 56, Echthromorpha atrata; 57, Lissopimpla excelsa; 58, Zatypota percontatoria.
Figures 87–90 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figures 87–90. Hind end of mesosoma with hind legs and metasoma dis-articulated; 87, Neotheronia mellosa; 88, Pimpla sumichrasti; 89, Scambus annulatus; 90, Dolichomitus annuicornis.
Figures 41–46 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figures 41–46. Stereoscan photographs of Pimplinae. Fig. 41, Sinarachna pallipes, head, posterior. Fig. 42, Dreisbachia avivae, mandible. Figs 43–46, Head, lateral; 43, Dolichomitus irritator, 44, Zaglyptus simonis; 45, Echthromorpha atrata; 46, Hymenoepimecis bicolor.
Figures 71–76 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figures 71–76. Stereoscan photographs of Pimplinae. Figs 71, 72, tergites II—IV, dorsal; 71, Polysphincta tuberosa; 72, Zatypota petronae. Figs 73–75, apex of ovipositor; 73, Liotryphon crassiseta; 74, Endromopoda detrita; 75, Dolichomitus imperator. Fig. 76, Zatypota petronae, ovipositor entire.
Figures 23–28 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figures 23–28. Stereoscan photographs of Pimplinae, head, anterior; 23, Ephialtes manifestator; 24, Paraperithous gnathaulax; 25, Xanthephialtes oculatus; 26, Schizopyga frigida; 27, Theronia melanocera ♀; 28, Theronia melanocera ♂.
Figures 47–52 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figures 47–52. Stereoscan photographs of Pimplinae, pronotum, lateral; 47, Dolichomitus irritator; 48, Pimpla azteca; 49, Schizopyga frigida; 50, Clistopyga calixtoi; 51, Hymenoepimecis bicolor; 52, Acrodactyla degener.
Figure 22 in The suprageneric groups of the Pimplinae (Hymenoptera: Ichneumonidae): a cladistic re-evaluation and evolutionary biological study
Figure 22. Cladogram resulting from secondary analysis: section 9 (of 9), the Polysphincta genus-complex. Although there are some similarities in topology with the primary analysis (Figs 11–13) – such as the basal position of Piogaster and the composition of two more derived clades – all genera are apparently monophyletic.
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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.
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.