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8 results for “Physisporinus”
FIGURE 2 in Physisporinus yunnanensis sp. nov. (Polyporales, Basidiomycota) from Southern China
FIGURE 2. Basidiomata of Physisporinus yunnanensis. Bars: A = 1 cm, B = 1 mm (Holotype: CLZhao 21647). Photoplate by: Jia Cai.
FIGURE 3 in Physisporinus yunnanensis sp. nov. (Polyporales, Basidiomycota) from Southern China
FIGURE 3. Microscopic structures of Physisporinus yunnanensis (drawn from the holotype, CLZhao 21647). A: Basidiospores. B: Basidia and basidioles. C: Cystidioles. D: Cystidia and hypha-like cystidia. E: Hyphae from subiculum. F: Hyphae from trama. Bars: A = 5 µm; B–F = 10 µm. Drawings by: Jia Cai.
FIGURE 1 in Physisporinus yunnanensis sp. nov. (Polyporales, Basidiomycota) from Southern China
FIGURE 1. Maximum Parsimony strict consensus tree illustrating the phylogeny of one new species of Physisporinus based on ITS+nLSU sequences. Branches are labeled with maximum likelihood bootstrap values equal to or higher than 70%, parsimony bootstrap values equal to or higher than 50% and Bayesian posterior probabilities equal to or higher than 0.95.
Fig. 5 in Lanostane triterpenoids from the fungus Physisporinus vitreus and their inhibitory activity against nitric oxide production
Fig. 5. Effects of compound 2 on TNF-α, iNOS and IL-1β mRNA expression in LPS-activated RAW 264.7 cell lines. *** denotes significant differences from the control group with P <0.001; ## and ### denote significant differences from LPS group with P <0.01 and 0.001, respectively. All data are presented as the mean ± SEM (n = 3).
Fig. 4 in Lanostane triterpenoids from the fungus Physisporinus vitreus and their inhibitory activity against nitric oxide production
Fig. 4. Calculated ECD spectra and experimental spectra of compound 1.
Fig. 3 in Lanostane triterpenoids from the fungus Physisporinus vitreus and their inhibitory activity against nitric oxide production
Fig. 3. Key ROESY correlations of compounds 1–8.
Fig. 2. Key HMBC and 1H–1H in Lanostane triterpenoids from the fungus Physisporinus vitreus and their inhibitory activity against nitric oxide production
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–8.
Fig. 1 in Lanostane triterpenoids from the fungus Physisporinus vitreus and their inhibitory activity against nitric oxide production
Fig. 1. Structures of compounds 1–12 isolated from P. vitreus.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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