Bacterial community information at the genus level in the rhizosphere soil of continuous monocropping passion fruit plants. by Weiwei Lin (2442850)

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Variation in the content of phenolic acids in rhizosphere soil of continuously monocultured passion fruit plants. by Weiwei Lin (2442850)

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The content of rhizosphere soil enzymes in passion fruit with different growth years. by Weiwei Lin (2442850)

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Basic physicochemical properties of rhizosphere soil of continuous cropping passion fruit. by Weiwei Lin (2442850)

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The differences in the structural composition of rhizosphere soil bacterial communities of passion fruit with different growth years. by Weiwei Lin (2442850)

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The effect of continuous monocropping of passion fruit plant on rhizosphere soil enzyme activity. by Weiwei Lin (2442850)

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The chessboard scoring of rhizosphere soil bacterial colonies in passion fruit with different growth years. by Weiwei Lin (2442850)

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In situ analysis of total bacteria and fungi in the rhizosphere soil of passion fruit under continuous monocropping treatment. by Weiwei Lin (2442850)

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The weighted UniFrac (A) and PCoA (B) analysis of bacterial samples in passion fruit rhizosphere soil. by Weiwei Lin (2442850)

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Richness and diversity index of bacterial community in the rhizosphere soil of passion fruit under continuous monocropping treatment. by Weiwei Lin (2442850)

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The differences in OTU composition of rhizosphere soil bacterial communities of passion fruit with different growth years. by Weiwei Lin (2442850)

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Analysis of community heatmap at the genus level of dominant bacteria in the rhizosphere soil of continuous cropping passion fruit. by Weiwei Lin (2442850)

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Chessboard score of rhizosphere soil colonies of continuous cropping passiflora edulis. by Weiwei Lin (2442850)

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Early IL-33 administration increases trTregs and ILC2 numbers but does not enhance parasite-specific CD8+ T cells at 10 days post infection. by Santiago Boccardo (5927954)

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<b>Addition root exudates increase microbial biomass but decreases diversity and richness.</b> by Xiaochong Zhang (21179348)

Image 2_G. vaginalis increases HSV-2 infection by decreasing vaginal barrier integrity and increasing inflammation in vivo.tif by Nuzhat Rahman (16660416)

“…</p>Results<p>G. vaginalis inoculated mice infected with HSV-2 had significantly decreased survival rates, increased pathology, and higher viral titers than PBS and L. crispatus inoculated mice. …”

Image 5_G. vaginalis increases HSV-2 infection by decreasing vaginal barrier integrity and increasing inflammation in vivo.tif by Nuzhat Rahman (16660416)

“…</p>Results<p>G. vaginalis inoculated mice infected with HSV-2 had significantly decreased survival rates, increased pathology, and higher viral titers than PBS and L. crispatus inoculated mice. …”

Image 3_G. vaginalis increases HSV-2 infection by decreasing vaginal barrier integrity and increasing inflammation in vivo.tif by Nuzhat Rahman (16660416)

“…</p>Results<p>G. vaginalis inoculated mice infected with HSV-2 had significantly decreased survival rates, increased pathology, and higher viral titers than PBS and L. crispatus inoculated mice. …”

Image 1_G. vaginalis increases HSV-2 infection by decreasing vaginal barrier integrity and increasing inflammation in vivo.tif by Nuzhat Rahman (16660416)

“…</p>Results<p>G. vaginalis inoculated mice infected with HSV-2 had significantly decreased survival rates, increased pathology, and higher viral titers than PBS and L. crispatus inoculated mice. …”

Image 4_G. vaginalis increases HSV-2 infection by decreasing vaginal barrier integrity and increasing inflammation in vivo.tif by Nuzhat Rahman (16660416)

“…</p>Results<p>G. vaginalis inoculated mice infected with HSV-2 had significantly decreased survival rates, increased pathology, and higher viral titers than PBS and L. crispatus inoculated mice. …”