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Figure 3 in Comparing the effectiveness of pitfall traps and active sampling methods for ants and spiders in a Chromolaena odorata invaded site
Figure 3. Spider species richness collected using active and passive sampling techniques in Buffelsdraai Conservancy [AHC = aerial hand collection above the knee; AHC CRYPTIC = aerial hand collection below the knee cryptic; AHC OBV = aerial hand collection below the knee noticeable or non-cryptic; BB = vegetation beating].
Figure 8 in Molecular docking studies and evaluation of the antiretroviral activity and cytotoxicity of the species Lafoensia pacari Saint-Hilaire
Figure 8. Representation of complex isosurface (A, C, and E) and 2D interactions within the enzyme active site (B, D, and F): AG/5TIQ (A, B); AE/5TIQ (C, D); PU/5TIQ (E, F).
Figure 7 in Molecular docking studies and evaluation of the antiretroviral activity and cytotoxicity of the species Lafoensia pacari Saint-Hilaire
Figure 7. Representation of complex ribbons (A, C, and E) and 2D interactions within the enzyme active site (B, D, and F): AG/5TIQ (A, B); AE/5TIQ (C, D); PU/5TIQ (E, F).
Figure 4 in Molecular docking studies and evaluation of the antiretroviral activity and cytotoxicity of the species Lafoensia pacari Saint-Hilaire
Figure 4. Spectra of 1H-NMR (A) and J-resolved 1H-1H (B) expanded on the region of aromatic signals of the acetanolic subfraction - washing water - acids (88.82%) of L. pacari obtained in methanol-d4.
Figure 3 in Molecular docking studies and evaluation of the antiretroviral activity and cytotoxicity of the species Lafoensia pacari Saint-Hilaire
Figure 3. (A) Scores of PCA (71.5% PC1 and 21.3% PC2) of 6 subfractions obtained from the ethanolic extract of L. pacari classified by (RT%) activity of each subfraction. (B) Loadings from PC1 (71.5%) with NMR signals discriminating between subfractions.
Figure 5. Spectrum region HSQC 1H-13C in Molecular docking studies and evaluation of the antiretroviral activity and cytotoxicity of the species Lafoensia pacari Saint-Hilaire
Figure 5. Spectrum region HSQC 1H-13C (A) and HMBC 1H-13C (B) with region of aromatics compounds of the acid wash water acetate subfraction (88.83%) of L. pacari obtained in methanol-d4.
Figure 2 in Molecular docking studies and evaluation of the antiretroviral activity and cytotoxicity of the species Lafoensia pacari Saint-Hilaire
Figure 2. Scores of PCA of obtained subfractions from the ethanolic extract of L.pacari classified by the (RT%) activity of each subfraction.
Figure 1 in Molecular docking studies and evaluation of the antiretroviral activity and cytotoxicity of the species Lafoensia pacari Saint-Hilaire
Figure 1. Profile of 1H-NMR spectra of subfractions obtained from the ethanolic extract of L. pacari classified by (RT%) activity of each subfraction.
Figure 5. 3D in Studies on the recombinant production and anticancer activity of thermostable L- asparaginase I from Pyrococcus abyssi
Figure 5. 3D structure of L-asparaginase, α-helices are shown in red, β-pleated sheets in yellow. The interaction of enzyme and L-asparagine is shown, ligand atoms are shown in balls at active site.
Figure 4 in Studies on the recombinant production and anticancer activity of thermostable L- asparaginase I from Pyrococcus abyssi
Figure 4. Lineweaver-Burk plot indicating used for the calculation of KM and Vmax of recombinant L-asparaginase.
Figure 3 in Studies on the recombinant production and anticancer activity of thermostable L- asparaginase I from Pyrococcus abyssi
Figure 3. Effect of pH on the enzyme activity. The pH value for optimum enzyme activity was found 8.
Figure 6 in Studies on the recombinant production and anticancer activity of thermostable L- asparaginase I from Pyrococcus abyssi
Figure 6. ConSurf generated conserved sequences of L-asparaginase gene, the active site residues associated with interaction of ligand are shown in boxes.
Figure 1. SDS-PAGE photograph. M in Studies on the recombinant production and anticancer activity of thermostable L- asparaginase I from Pyrococcus abyssi
Figure 1. SDS-PAGE photograph. M, Protein marker; E, cellular extract from experimental culture; F1 and F2, purified enzyme fractions collected from chromatography colum; C, negative control experiment (extract of cells transformed with plasmid without gene of interest).
Figure 5 in Antinociceptive and anti-inflammatory activities of Hymenaea martiana Hayne (Fabaceae) in mice
Figure 5. Effect of the ethyl acetate fraction of Hymenaea martiana (Hm-AcOEt - 100, 200 and 400 mg.kg-1), indomethacin (20 mg. kg-1) and morphine (10 mg.kg-1) on formalin test in mice. Values are mean ± S.E.M.; **P <0.01, significantly different from control; one-way ANOVA followed by Tukey's test (n = 6, per group). (a) first phase and (b) second phase.
Figure 7 in Antinociceptive and anti-inflammatory activities of Hymenaea martiana Hayne (Fabaceae) in mice
Figure 7. Effect of the ethyl acetate fraction of Hymenaea martiana (Hm-AcOEt - 100, 200 and 400 mg.kg-1), Hm-EtOH (200 mg.kg-1) + naloxone and morphine (10 mg.kg-1) on the hot-plate test in mice. Values are mean ± S.E.M.; *P <0.05, **P <0.01, significantly different from control; two-way ANOVA followed by Bonferroni's multiple comparisons test (n = 6, per group).
Figure 6 in Antinociceptive and anti-inflammatory activities of Hymenaea martiana Hayne (Fabaceae) in mice
Figure 6. Effect of the ethanolic extract of Hymenaea martiana (Hm-EtOH - 100, 200 and 400 mg.kg-1), Hm-EtOH (200 mg.kg-1) + naloxone and morphine (10 mg.kg-1) in the hot-plate test in mice. Values are mean ± S.E.M.; *P <0.05, ** P <0.01, significantly different from control; two-way ANOVA followed by Bonferroni's multiple comparisons test (n = 6, per group).
Figure 11 in Antinociceptive and anti-inflammatory activities of Hymenaea martiana Hayne (Fabaceae) in mice
Figure 11. Effect of the ethyl acetate fraction of Hymenaea martiana (Hm-AcOEt - 100, 200 and 400 mg.kg-1) and dexamethasone (2 mg. kg-1) on leukocyte migration into the peritoneal cavity induced by carrageenan in mice. Values are mean ± S.E.M.; **P <0.01, significantly different from control; one-way ANOVA followed by Tukey's test (n = 6, per group).
Figure 8 in Pouteria ramiflora leaf extract on emulgel in wound healing activity in diabetic rats
Figure 8. Photomicrograph of histological sections of rats' skin wounds of Control group (Carbopol) (A, B, and C), Ethanolic extract (Ext) (D, E, F) and Gel + Ethanolic extract 2% (Ext+gel) (G, H, I) at 30 days after the skin wound injury (D, E, F). epidermis (ep); granular layer (green arrow); fibroblasts (black arrow). HE.
Figure 5 in Pouteria ramiflora leaf extract on emulgel in wound healing activity in diabetic rats
Figure 5. Quantification of inflammatory cells, fibroblasts, and angiogenesis (blood vessels) in diabetic animals' skin on groups: Control, Ext and Ext+gel, 14 days. ns (statistically not significant). DUNN's test (P=0.05).
Figure 4 in Pouteria ramiflora leaf extract on emulgel in wound healing activity in diabetic rats
Figure 4. Photomicrograph of histological sections of diabetic rats' skin wounds. (A, A1), Control, Ext (B, B1) and Ext+gel (C, C1) to 14 days after injury of the skin wound. Epidermis (ep); keratin (k); fibroblast (f); collagen fibers (c); HE. Quantification of inflammatory cells, fibroblasts, and angiogenesis in diabetic animals' skin on groups: Control, Ext and Ext+gel, DUNN's test (P=0.05).
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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.