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6,818 results for “inhibition”
Figure 4 in Blue and red light photoemitters as approach to inhibit Staphylococcus aureus and Pseudomonas aeruginosa growth
Figure 4. Effect of blue and red light on S. aureus e P. aeruginosa diluted in saline solution (0.9% NaCl) applied for a period of 3 hours. *Statistically significant difference using Mann-Whitney U test (p <0.05) between blue light exposed group and control groups.
Figure 2 in Blue and red light photoemitters as approach to inhibit Staphylococcus aureus and Pseudomonas aeruginosa growth
Figure 2. Diameter of S.aureus and P. aeruginosa surviving colonies after exposure to blue and red light for 6 hours and incubated for 24 hours (A) and 48 hours (B). *Statistically significant difference using Mann-Whitney U test (p <0.05) for independent samples.
Figure 1 in Sensitivity to salinity at the emergence and seedling stages of barnyardgrass (EchinochloQ crus-gQlli), weedy rice (OryzQ sQtivQ), and rice with different tolerances to ALS-inhibiting herbicides
Figure 1. Dose–response emergence curve with the average data points of the different Echinochloa crus-galli populations against the salt concentration. Curve parameter estimates (Equation 1): s1 (b = 1.94, d = 55.85, e = 287.76), s2 (b = 1.52, d = 89.91, e = 222.71), s3 (b = 1.13, d = 89.91, e = 282.58), r1(b = 3.96, d = 67.67, e = 196.55), r2 (b = 6.85, d = 94.64, e = 123.58). The salt concentration required to reduce emergence by 50% (EC50) is shown below the graph. Only the significant pairwise comparisons between EC50 (SI index) are shown (Equation 2).
Figure 2 in Sensitivity to salinity at the emergence and seedling stages of barnyardgrass (EchinochloQ crus-gQlli), weedy rice (OryzQ sQtivQ), and rice with different tolerances to ALS-inhibiting herbicides
Figure 2. Dose–response emergence curve with the average data points of the different Oryza sativa (weedy rice) populations and rice varieties against the salt concentration. Curve parameter estimates (Equation 1): wr1 (b = 9.40, d = 87.14, e = 195.80), wr2 (b = 9.40, d = 87.14, e = 160.19), wr3 (b = 8.49, d = 89.73, e = 173.01), Baldo (b = 4.81, d = 87.12, e = 146.49), CL80 (b = 3.08, d = 60.89, e = 140.04). The salt concentration required to reduce the emergence by 50% (EC50) and the significant pairwise comparisons between EC50 (SI index) are shown below the graph (Equation 2).
Figure 1 in Ability of Sterile Males to Inhibit Female Remating in the Oriental Fruit Fly, Bactrocera dorsalis (Hendel) (Diptera: Tephritidae)
Figure 1. Numbers of rematings observed per cage for females first mated to fertile wild or sterile DTWP males at 3 intervals after the initial mating. Each cage held 10 test females. Symbols represent mean values + 1 SE; N = 8 in all cases.
Figure 3 in Mowing inhibits the invasion of the alien species Solidago altissima and is an effective management strategy
Figure 3. (a) Aboveground biomass of S. altissima in September 2019. (b) Biomass of rhizomes of S. altissima in September 2019. Mowing 1: mowed once in July; Mowing 2: mowed twice in May and September; Mowing 3: mowed three times in May, July, and September. Data are presented as means ± standard errors of 14 replicates. Bars with different letters are significantly different at p <0.05 (ANOVA with post hoc Tukey's test).
Figure 4 in Mowing inhibits the invasion of the alien species Solidago altissima and is an effective management strategy
Figure 4. Effects of control practices on flowering rates of S. altissima in October 2019. Mowing 1: mowed once in July; Mowing 2: mowed twice in May and September; Mowing 3: mowed three times in May, July, and September. Data are presented as means ± standard errors of 14 replicates. Bars with different letters are significantly different at p <0.05 (ANOVA with post hoc Tukey's test).
Figure 1 in Mowing inhibits the invasion of the alien species Solidago altissima and is an effective management strategy
Figure 1. (a) Coverage of S. altissima and (b) the average number of species per quadrat in the S. altissima-dominant areas or uninvaded areas. Data are presented as means ± standard errors of 14 replicates. Bars with different letters are significantly different at p <0.05 (Student's t-test).
Figure 2 in Mowing inhibits the invasion of the alien species Solidago altissima and is an effective management strategy
Figure 2. Number of shoots of S. altissima in March 2018 and April 2019. Mowing 1: mowed once in July; Mowing 2: mowed twice in May and September; Mowing 3: mowed three times in May, July, and September; Eco 200: 30% of shoots in the quadrats were cut near the ground, and the cut surfaces were covered with Eco 200 block. Data are presented as means ± standard errors of 14 replicates. Bars with different letters are significantly different at p <0.05 (ANOVA with post hoc Tukey's test).
Fig. 1 in In vitro Trypanosoma cruzi Growth Inhibition by Extremely Low-frequency Electromagnetic Fields
Fig. 1. Effect of 60 Hz sinusoidal magnetic fields at 2.0 mT and 24 h exposure on cell growth of T. cruzi epimastigote cultures. Bars represent arithmetical grouped means ± standard deviations.
Illumina Sequencing Data for "Elucidating human gut microbiota interactions that robustly inhibit diverse Clostridioides difficile strains across different nutrient landscapes"
<p>Illumina Sequencing Data for Sulaiman et al., "Elucidating human gut microbiota interactions that robustly inhibit diverse Clostridioides difficile strains across different nutrient landscapes".</p>
Fig. 5 in Female remating inhibition and fitness of Bactrocera dorsalis (Diptera: Tephritidae) associated with male accessory glands
Fig. 5. Fecundities of Bactrocera dorsalis females of various mating statuses. A. Lifetime mean number (± S.E.) of eggs laid per female, and B. Mean oviposition rates per week of Bactrocera dorsalis females of various mating statuses. G1, virgin females housed alone (n = 30); G2, females mated once (n = 26); G3, females mated twice with different virgin males (n = 32); G4, females mated with males that had mated on the previous day (n = 29); G5, females housed with males at a sex ratio of 1: 1 (n = 23); G6, females housed with males at a sex ratio of 1♀: 23 (n = 24). Different letters indicate significant differences.
Fig. 1 in Female remating inhibition and fitness of Bactrocera dorsalis (Diptera: Tephritidae) associated with male accessory glands
Fig. 1. Male accessory glands of Bactrocera dorsalis. One pair of long tube mesodermal accessory glands (MAG) and 3 pairs of long, convoluted, complex and fragile ectodermal accessory glands (EAG).
Fig. 6 in Female remating inhibition and fitness of Bactrocera dorsalis (Diptera: Tephritidae) associated with male accessory glands
Fig. 6. Fertilities of Bactrocera dorsalis females of various mating statuses. A. Lifetime mean percent hatch of eggs laid by females of G2 – G6 mating statuses, B. Mean percent hatch of eggs laid each week by females of G2 – G6 mating statuses. G2, females mated once (n = 18); G3, females mated twice with virgin males (n= 20); G4, females mated with non-virgin males (n = 18); G5, females housed with males with a sex ratio of 1: 1 (n = 18); G6, females housed with males with a sex ratio of 1♀: 23 (n = 19). Data for the unfertilized eggs laid by virgin females in group G1 and for females that produced fewer than 5 eggs in total were not analyzed. Different letters indicate significant differences.
Fig. 3 in Female remating inhibition and fitness of Bactrocera dorsalis (Diptera: Tephritidae) associated with male accessory glands
Fig. 3. Mean percentage of successful matings among Bactrocera dorsalis of different mating statuses. M1, matings of 8-day old virgin females with of 8-day old virgin males on day 1; M2, matings of 9-day old virgin females with 9-day old virgin males on day 2; M3, matings of 10-day old virgin females with 10-day old males on day 3; M4, matings on day 2 of virgin females with males that had mated on day 1; M5, both first and second matings with virgin males; M6, first mating to non-virgin male and remating to virgin male. Different letters indicate significantly different proportions.
Response inhibition in the water skink
<p>All datasets and R code used during analysis (in order of analysis)</p>
Fig. S2. E in Comparison of in vitro methods to inhibit growth of a virulent strain of Batrachochytrium dendrobatidis (Longcore, Pessier, and Nichols 1999)
Fig. S2. E. coli-violacein transformations. Violacein gene transformations of E. coli. (A) Example of NEB5-alpha-pJP1000 colony growth after 24 h post heat shock transformation. Each week, transformants were passed by re-streaking onto fresh agar and incubated at 37 °C for 24 h. (B) NEB5-alpha-pPSXvio+, (C) NEB5-alpha-pPSXvio++.
Fig. 3 in Comparison of in vitro methods to inhibit growth of a virulent strain of Batrachochytrium dendrobatidis (Longcore, Pessier, and Nichols 1999)
Fig. 3. Microscopic images (40x) of Bd challenge assays. (A) Microbacterium, (B) Micrococcaceae, and (C) recombinant E. coli- vio+. Vertical arrows point to the Bd lawn and horizontal arrows point to the left side of the bacterial streak. Absence of Bd lawn within field of view indicates the inhibitory effect from the bacterial streak. Approximate diameter of field of view ~0.5 mm.
Fig. S1. Toad skin swab cultures. Culture plates from A in Comparison of in vitro methods to inhibit growth of a virulent strain of Batrachochytrium dendrobatidis (Longcore, Pessier, and Nichols 1999)
Fig. S1. Toad skin swab cultures. Culture plates from A. boreas skin swabs after three days incubation at 25 °C.
Fig. 1. The Kruskal-Wallis rank sum test for the boxplot returned a in Comparison of in vitro methods to inhibit growth of a virulent strain of Batrachochytrium dendrobatidis (Longcore, Pessier, and Nichols 1999)
Fig. 1. The Kruskal-Wallis rank sum test for the boxplot returned a chi-squared value = 2, degrees of freedom (df) = 2, and P = 0.3679. The Wilcoxon rank sum test for the positive control and the highest concentration of amphotericin B returned W = 9, P = 0.1. These analyses show that the alternative hypothesis is true and assumes that there is information in the magnitudes and signs of the differences between paired observations, because the mean (location shift) is not equal to 0. Observed differences in mean cell count between the three groups (0.0, 1.6, and 3.2 µg/mL) are not statistically significant (P> 0.05).
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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