The introduction of mutualisms into assembled communities increases their connectance and complexity while decreasing their richness. by Gui Araujo (22170819)

“…When they stop being introduced in further assembly events (i.e. introduced species do not carry any mutualistic interactions), their proportion slowly decreases with successive invasions. …”

Loss of ECRG4 expression decreases neutrophil mobilization from bone marrow reserves. by Katie D. Pool (20141584)

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The distribution of <i>Giardia duodenalis</i> assemblages in domestic and wild populations of nonhuman mammalian species with a larger number of isolates. by Kareem Hatam-Nahavandi (7384790)

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Biases in larger populations. by Sander W. Keemink (21253563)

“…Threshold parameter <i>c</i> = − 0 . 1 for the rectified cosine tuning with 4 neurons, and width <i>w</i> was 1 for von Mises tuning. …”

Percentage of exhale flux penetrating through the mask fabric for different values of <i>c</i>_<i>k</i>; a–c and d–f decreasing porosity for outward and inward protection model respectively; <i>k</i>_<i>L</i> is head loss coefficient for inward protection model. by Akshay Anand (118579)

<i>In vivo</i> and long-term chaperone activity assessment of wild-type and p.R163C mutant αB-crystallin. by Aref Baharvand (21713886)

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<i>ΔG°</i> and C_1/2 values of various αB-crystallin samples derived from equilibrium urea unfolding analysis. by Aref Baharvand (21713886)

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Contribution of the through-mask leakages from the cavity and channel network distributed along the periphery of the mask; a–c and d–f are decreasing porosity <i>c</i>_<i>k</i> = 100,500,1000 (<i>kg</i>/<i>m</i>² <i>s</i>) for outward protection (with nose clips) and inward protection model, respectively; the <i>k</i>_<i>L</i> for inward protection model is 0.5. by Akshay Anand (118579)

“…<p>Contribution of the through-mask leakages from the cavity and channel network distributed along the periphery of the mask; a–c and d–f are decreasing porosity <i>c</i>_<i>k</i> = 100,500,1000 (<i>kg</i>/<i>m</i>² <i>s</i>) for outward protection (with nose clips) and inward protection model, respectively; the <i>k</i>_<i>L</i> for inward protection model is 0.5.…”

Time course of Path Length, LFS and Velocity during postural training. by Cristina Dolciotti (16317330)

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Time course of 95% Area, X and Y Amplitude Sway during postural training. by Cristina Dolciotti (16317330)

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Between-group differences in 95% Area, Y Sway Amplitude and LFS during postural training. by Cristina Dolciotti (16317330)

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Consolidation of training-induced changes in unipedal stance: 95% Area, Y Sway Amplitude and LFS. by Cristina Dolciotti (16317330)

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Consolidation of training-induced changes in unipedal stance: Path Length, X Sway Amplitude and Velocity. by Cristina Dolciotti (16317330)

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Fluorescence analysis of wild-type and p.R163C αB-crystallin proteins. by Aref Baharvand (21713886)

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Spectroscopic characterization of wild-type and p.R163C αB-crystallin: CD, FTIR and Raman analysis. by Aref Baharvand (21713886)

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Raman spectroscopy was employed to investigate the conformational variations between wild-type and p.R163C mutant αB-crystallin proteins. by Aref Baharvand (21713886)

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Thioflavin-T (ThT) fluorescence analysis of amyloid fibril formation in wild-type and p.R163C mutant αB-crystallin under thermochemical stress. by Aref Baharvand (21713886)

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Root-mean-square fluctuation (RMSF) analysis of wild-type and p.R163C mutant αB-crystallin dimers from molecular dynamics simulations. by Aref Baharvand (21713886)

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Chemical, thermal, and proteolytic stability of αB-crystallin proteins. by Aref Baharvand (21713886)

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Establishment of cBu-1 BAC16 for the isolation of reactivated cell population. by Tomoki Inagaki (12903779)

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