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

“…(D) As a result, the introduction of mutualistic interactions promotes a growth in complexity in communities where it was once established as low, while stopping the introduction of further mutualistic interactions causes a slight decrease in complexity. …”

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

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)

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. …”

Time course of Path Length, LFS and Velocity 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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Time course of 95% Area, X and Y Amplitude Sway during postural training. 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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Consolidation of training-induced changes in unipedal stance: 95% Area, Y Sway Amplitude and LFS. by Cristina Dolciotti (16317330)

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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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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.…”

Cephalometric measurement points. by Lijuan Liu (136685)

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Participant demographics. * P-values were determined using Fisher-Freeman-Halton test when contingency tables are larger than 2 × 2. by Elie Mulhem (22537863)

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

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Naringenin decreases total cell viability. by Lauren A. Eanes (20995499)

Lifespan of a single <i>T. utriculata</i> rosette. by Alexandra M. Campbell (3284094)

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

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Hydrogen volume fraction distribution at different pressures (a) 1 MPa; (b) 3 MPa; (c) 5 MPa. by Weiqing Xu (1279959)

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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