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54,099 results for “Expression”
Fig 3 in Colossoma macropomum (Characiformes: Serrasalmidae) adapted to new climate regime: differential gene expression from farmed tambaqui juveniles raised in subtropical and tropical regions
Fig 3: IBR analyses of relative gene expression in Balbina (BA) and Brumado (BRU) populations. The IBR values are 42.7 (Balbina) and 6.79 (Brumado).
Fig 2 in Colossoma macropomum (Characiformes: Serrasalmidae) adapted to new climate regime: differential gene expression from farmed tambaqui juveniles raised in subtropical and tropical regions
Fig 2: Heatmap of relative expression in Balbina (BA) and Brumado (BRU) populations. The colour scale ranges from blue (low transcript levels) to red (high transcript levels).
Figure 3 in Effect of Vicia sativa L. on Motility, Mortality and Expression Levels of hsp Genes in J2 Stage of Meloidogyne hapla
Figure 3: Influence of Vicia sativa cv. Ina diffusate treatment on Hsp gene expression in Meloidogyne Hapla J2 stage. Each value represents the mean ± s.d. of three biological replicates. The expression levels are indicated as the fold-change normalized to the control (untreated diffusate), normalized to the value of 1 (dashed line). Values were expressed as the mean fold difference, and statistically significant differences between treated and control samples are shown; *p≤0.01 based on t-Student test.
Figure 2 in Effect of Vicia sativa L. on Motility, Mortality and Expression Levels of hsp Genes in J2 Stage of Meloidogyne hapla
Figure 2: Distribution of 36 combinations of temperatures, cultivars, and variants in the space of the first two canonical variables.
Figure 1 in Effect of Vicia sativa L. on Motility, Mortality and Expression Levels of hsp Genes in J2 Stage of Meloidogyne hapla
Figure 1: Dendrogram of the nearest neighbour cluster grouping of combinations of temperature, cultivars, and variants on the basis of four traits.
FIG. 5 in Expressed sex ratio in populations of the moss Hamatocaulis vernicosus (Mitt.) Hedenäs (Scorpidiaceae) in the Czech Republic with consideration of its cryptic species
FIG. 5. — The sex ratio in mixed population at locality Zhůří 1. Unbordered pie charts refer to clade 1, bordered ones represent clade 2. The patch in the larger circle contained plants of both clades, so this patch must be excluded from evaluating sex ratio in separated clades.
FIG. 3 in Expressed sex ratio in populations of the moss Hamatocaulis vernicosus (Mitt.) Hedenäs (Scorpidiaceae) in the Czech Republic with consideration of its cryptic species
FIG. 3. — Rates of male (blue), female (red) and non-expressing (green) plants at studied localities of Hamatocaulis vernicosus (Mitt.) Hedenäs clade 1 and 2.
FIG. 2 in Expressed sex ratio in populations of the moss Hamatocaulis vernicosus (Mitt.) Hedenäs (Scorpidiaceae) in the Czech Republic with consideration of its cryptic species
FIG. 2. — The expressed sex ratio at studied localities of H. vernicosus (Mitt.) Hedenäs. In mixed populations,only single-clade patches were used for the assessment.
FIG. 4 in Expressed sex ratio in populations of the moss Hamatocaulis vernicosus (Mitt.) Hedenäs (Scorpidiaceae) in the Czech Republic with consideration of its cryptic species
FIG. 4.— Sex ratio at localities with co-occurring cryptic species. All, without distinguished clades; cl. 1, clade 1; cl. 2, clade 2; Šimanov, Šimanovské rašeliniště. Only barcoded shoots were used to create this graph.
FIG. 1 in Expressed sex ratio in populations of the moss Hamatocaulis vernicosus (Mitt.) Hedenäs (Scorpidiaceae) in the Czech Republic with consideration of its cryptic species
FIG. 1.— The sex expression of Hamatocaulis vernicosus (Mitt.) Hedenäs in the Czech Republic at individual localities assessed at two levels of pooling hierarchy ("shoots at localities" and "patches at localities").
FIG. 4 in Dimorphic sexual expression and anisospory in Homalothecium sericeum Schimp. s.l. (Brachytheciaceae) in Portugal
FIG. 4. — Graphical presentation of spore sizes from 12 different capsules of selected samples. Variation of spore sizes in six capsules of Homalothecium sericeum (Hedw.) Schimp. s.s (left graphics) and six capsules of H. meridionale (M. Fleisch. & Warnst.) Hedenäs (right graphics). Numbers on the vertical axes indicate frequencies, and those on the horizontal axes indicate diameter values in µm. The dashed line represents the tendency line bimodal distribution of diameter values. The dark grey horizontal bars in left side of each histogram, indicate the size range of collapsed spores, measured in the same capsule (capsules from LISU*collection, displayed sequentially for localities from the North to the South of Portugal).
FIG. 3 in Dimorphic sexual expression and anisospory in Homalothecium sericeum Schimp. s.l. (Brachytheciaceae) in Portugal
FIG. 3. — Spores photographed under scanning electron microscopy to reveal the anisosporic condition observed in individual capsules of two Homalothecium Schimp. species (H. sericeum (Hedw.) Schimp. s.s. and H. meridionale (M. Fleisch. & Warnst.) Hedenäs) from herbarium samples: A, B, from capsules of H. sericeum s.s. (LISU 262054 and LISU 264096); C, D, from capsules of H. meridionale (LISU 265335 and LISU 266570). Scale bars: 10 µm.
FIG. 2 in Dimorphic sexual expression and anisospory in Homalothecium sericeum Schimp. s.l. (Brachytheciaceae) in Portugal
FIG. 2. — Synthesis of the observations of sexual expression in the two Homalothecium Schimp. species (H. sericeum (Hedw.) Schimp. s.s. and H. meridionale (M. Fleisch. & Warnst.) Hedenäs) in Portugal (from LISU herbarium and/or field observations): A, female young colony without sporophytes, but with mixed small male plants; B, small independent male plants; C, independent male plants with caducous branches; D, independent male with perigonia in small branch; E, detached perigonium with two antheridia; F, G, dwarf males attached as tiny epiphytes to the female leaf, originated directly from spores, generally observed acquiring basal rhizoids (G) and eventually originating independent male colonies (as B); H, female plants with sporophytes and probably with dwarf males; I, green spores of two different sizes and aborted brown spores mixed (from capsules of LISU 262312; LISU 264096 and LISU 262054); J, part of a sample with caducous branches from a herbarium specimen. Scale bar: A, B, C, J, 0.8 cm; D, F, 500 µm; E, 300 µm; G, 400 µm and 600 µm; H, 0.4 cm; I, ± 50 µm.
Figure 2 in Recombinant - and -tubulin from Echinococcus granulosus: expression, purification and polymerization
Figure 2. Sequence alignment of Echinococcus granulosus α9-tubulin and corresponding sequences from humans and parasites. The symbol ''*'' denotes the positions of amino acids that have a single, fully conserved amino acid residue; the symbol '':'' denotes conservation between groups of amino acids with strongly similar properties; the symbol ''.'' denotes conservation between groups of amino acids with weakly similar properties; and the symbol ''–'' denotes gaps inserted to maximize sequence alignment. EgA9, E. granulosus α9; HuA6, human alpha 6 (119578461); HmA5, H. microstoma alpha 5 (674586714); HcA, H. contortus alpha tubulin (159155); SjA1, S. japonicum alpha 1–3 (226478902); and TgA, T. gondii alpha (161937).
Figure 1 in Recombinant - and -tubulin from Echinococcus granulosus: expression, purification and polymerization
Figure 1. The cloning and expression of α9- and β4-tubulin. (a) The expression of α9- and β4-tubulin in E. coli BL21 (DE3). M: standard protein molecular weight marker, lane 1: negative control without induction, lane 2: induced control, lane 3: the supernatant after sonication, lane 4: the pellet after sonication, and lane 5: purified recombinant tubulin. (b) Western blot analysis. M: standard protein molecular weight marker, lane 1: α-tubulin, lane 2: β-tubulin.
Figure 3 in Recombinant - and -tubulin from Echinococcus granulosus: expression, purification and polymerization
Figure 3. The sequence alignment of Echinococcus granulosus β4-tubulin and corresponding sequences from humans and parasites. Symbol meanings are as in Figure 2. EgB4, E. granulosus β4-tubulin; EmB1, E. multilocularis Tub-1 gene (7838198); EmB2, E. multilocularis Tub-2 gene (7838200); EmB3, E. multilocularis Tub-3 gene (7838202); HuB3, human B3 (50592996); HuB4, human B4a (574584803); HmB2C, H. microstoma beta 2C (674589300); HcB1, H. contortus beta tubulin isotype 1 (124244617); SjB2, S. japonicum beta 2 (226467271); PfB, P. falciparum beta (160732).
Figure 5 in Recombinant - and -tubulin from Echinococcus granulosus: expression, purification and polymerization
Figure 5. The polymerization of Echinococcus granulosus α9- and β4-tubulin. (a) Spectrophotometric analysis of polymerization of E. granulosus α9- and β4-tubulin at different concentrations. (b) Confocal scanning laser micrographs of the polymerization product of recombinant tubulin showing immune reactivity to anti-α-tubulin/Alexa-Fluor 488 antibody and anti-β-tubulin/Alexa-Fluor 647 antibody. (I): Phase contrast view, (II): α-tubulin immuno-reactivity, (III): β-tubulin immune-reactivity. (c) The microtubule-like structure resulting from polymerization of pure expressed α9- and β4-tubulin under appropriate conditions in vitro.
Figure 4 in Recombinant - and -tubulin from Echinococcus granulosus: expression, purification and polymerization
Figure 4. Modelled structure of the polymerized Echinococcus granulosus α9- and β4-tubulin dimer based on PDB ID 4f6r.
Figure 2. Flufenacet degradation 24 h in Flufenacet activity is affected by GST inhibitors in blackgrass (Alopecurus myosuroides) populations with reduced flufenacet sensitivity and higher expression levels of GSTs
Figure 2. Flufenacet degradation 24 h after treatment with different inhibitors in the sensitive Alopecurus myosuroides population Herbiseed-S (A) and population Kehdingen1 with reduced flufenacet efficacy (B). Different letters indicate significant differences in flufenacet degradation between treatments,and asterisks (*) indicate significant differences between the two populations for each treatment (P ≤ 0.05).
Figure 4 in Flufenacet activity is affected by GST inhibitors in blackgrass (Alopecurus myosuroides) populations with reduced flufenacet sensitivity and higher expression levels of GSTs
Figure 4. Expression of three tau-class glutathione transferases (GST1, GST2,GST3), two phi-class GSTs (GST4, GST5), and a theta-class isoform (GST6) differentially expressed in the sensitive Alopecurus myosuroides populations Herbiseed-S and Appel-S and the populations Kehdingen1 and Kehdingen2 with reduced flufenacet efficacy. Different letters indicate significant differences between populations (false discovery rate ≤ 0.05). TMM, trimmed mean of M values.
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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)
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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.