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46 results for “Xylaria”
Fig. 9 in Xylarinaps A-E, five pairs of naphthalenone derivatives with neuroprotective activities from Xylaria nigripes
Fig. 9. Effects of compounds 1–5 on GSH-Px in OGD-induced PC12 cells. The values represent mean ± SD (n =6). *P <0.05, **P <0.01 vs. the control group; #P <0.05, ##P <0.01 vs. the model group.
Fig. 6 in Xylarinaps A-E, five pairs of naphthalenone derivatives with neuroprotective activities from Xylaria nigripes
Fig. 6. Effects of compounds 1–5 on cell viability in OGD-induced PC12 cells. The values represent mean ± SD (n = 6). *P <0.05, **P <0.01 vs. the control group; #P <0.05, ##P <0.01 vs. the model group.
Draft genome sequence of Xylaria bambusicola isolate GMP-LS, the root and basal stem rot pathogen of sugarcane in Indonesia
<p>Supplementary Figure 1</p><p>Supplementary Table 1</p><p>Supplementary Table 2</p>
Figure 4 from: Pan X-Y, Song Z-K, Qu Z, Liu T-D, Ma H-X (2022) Three new Xylaria species (Xylariaceae, Xylariales) on fallen leaves from Hainan Tropical Rainforest National Park. MycoKeys 86: 47-63. https://doi.org/10.3897/mycokeys.86.71623
Figure 4 Xylaria polysporicola (FCATAS 848, holotype) a, b stromata on leaves (b, FCATAS 851) c stromatal surface d section through stroma, showing perithecia e, g asci and ascal apical ring in Melzer's reagent f, i ascal apical ring in Melzer's reagent h asci in black India ink j ascospore with germ slit in 1% SDS k, l ascospore in water m, n ascospore showing a slimy sheath and non-cellular appendages in India ink (FCATAS 850) o Ascospore in 1% SDS. Scale bars: 1 cm (a, b); 0.2 mm (c, d); 10 µm (e–o).
Figure 3 from: Pan X-Y, Song Z-K, Qu Z, Liu T-D, Ma H-X (2022) Three new Xylaria species (Xylariaceae, Xylariales) on fallen leaves from Hainan Tropical Rainforest National Park. MycoKeys 86: 47-63. https://doi.org/10.3897/mycokeys.86.71623
Figure 3 Xylaria lindericola (FCATAS 852, holotype) a, b stromata on leaves c fertile part of stroma d stromatal surface e section through stroma, showing perithecia f ascal apical ring and ascospores with beaked ends in Melzer's reagent g ascus and ascal apical ring in Melzer's reagent h ascus in water i, j ascospores in water k, l ascospore in Melzer's reagent m ascospore in India ink n ascospore in 1% SDS showing germ slit. Scale bars: 1.5 cm (a, b); 0.2 mm (c–e); 10 µm (f–n).
Figure 1 from: Pan X-Y, Song Z-K, Qu Z, Liu T-D, Ma H-X (2022) Three new Xylaria species (Xylariaceae, Xylariales) on fallen leaves from Hainan Tropical Rainforest National Park. MycoKeys 86: 47-63. https://doi.org/10.3897/mycokeys.86.71623
Figure 1 Phylogenetic tree of Xylaria based on multigene alignment of ITS-TUB-RPB2 in the Bayesian analysis. Bayesian posterior probabilities (≥ 0.95, before the slash markers) and RaxML bootstrap values (≥ 50, after the slash markers) are shown. Different clades are indicated as coloured blocks.
Figure 2 from: Pan X-Y, Song Z-K, Qu Z, Liu T-D, Ma H-X (2022) Three new Xylaria species (Xylariaceae, Xylariales) on fallen leaves from Hainan Tropical Rainforest National Park. MycoKeys 86: 47-63. https://doi.org/10.3897/mycokeys.86.71623
Figure 2 Xylaria hedyosmicola (FCATAS 856, holotype) a, b, e stromata on leaves (b, FCATAS 857) c stromatal surface d section through stroma, showing a perithecium f immature asci in water g, h ascal apical ring in Melzer's reagent i, j ascospores in Melzer's reagent k ascus in 1% SDS l, m asci and ascal apical ring in Melzer's reagent n ascospore in Melzer's reagent showing straight germ slit o ascospore in Melzer's reagent showing slightly sigmoid germ slit p, q ascospore showing a slimy sheath and non-cellular appendages in India ink. Scale bars: 1 cm (a, b); 0.1 mm (c, d); 0.5 mm (e); 20 µm (f, m); 10 µm (g–l, n–q).
Fig. 5 in Bioactive specialised metabolites from the endophytic fungus Xylaria sp. of Cudrania tricuspidata
Fig. 5. Calculated ECD or experimental ECD curves of 11.
Fig. 3 in Bioactive specialised metabolites from the endophytic fungus Xylaria sp. of Cudrania tricuspidata
Fig. 3. Calculated ECD or experimental ECD curves of 1a, 1b, 1c, 2a and 2b.
Fig. 4 in Bioactive specialised metabolites from the endophytic fungus Xylaria sp. of Cudrania tricuspidata
Fig. 4. Key NOESY correlations of compound 1c.
Fig. 1 in Bioactive specialised metabolites from the endophytic fungus Xylaria sp. of Cudrania tricuspidata
Fig. 1. Structures of compounds 1–13.
Fig. 3 in Polyhydroxylated sesquiterpenes and ergostane glycosides produced by the endophytic fungus Xylaria sp. from Azadirachta indica
Fig. 3. Key NOE correlations of compounds 1, 2 and 4–6.
Fig. 1 in Polyhydroxylated sesquiterpenes and ergostane glycosides produced by the endophytic fungus Xylaria sp. from Azadirachta indica
Fig. 1. Chemical structures of compounds 1–6.
Fig. 4. X in Polyhydroxylated sesquiterpenes and ergostane glycosides produced by the endophytic fungus Xylaria sp. from Azadirachta indica
Fig. 4. X-ray crystallographic structure of compound 1.
Fig. 2. Key HMBC and 1H–1H in Polyhydroxylated sesquiterpenes and ergostane glycosides produced by the endophytic fungus Xylaria sp. from Azadirachta indica
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1, 2 and 4–6.
Fig. 5. Proposed biosynthetic pathways for 1 in Xylarinaps A-E, five pairs of naphthalenone derivatives with neuroprotective activities from Xylaria nigripes
Fig. 5. Proposed biosynthetic pathways for 1.
Fig. 4 in Xylarinaps A-E, five pairs of naphthalenone derivatives with neuroprotective activities from Xylaria nigripes
Fig. 4. Experimental and calculated ECD spectra of compounds 4–5.
Fig. 3 in Xylarinaps A-E, five pairs of naphthalenone derivatives with neuroprotective activities from Xylaria nigripes
Fig. 3. Experimental and calculated ECD spectra of compounds 1–3.
Fig. 1 in Xylarinaps A-E, five pairs of naphthalenone derivatives with neuroprotective activities from Xylaria nigripes
Fig. 1. Structures of compounds 1–5.
Fig. 2. Key 2D in Xylarinaps A-E, five pairs of naphthalenone derivatives with neuroprotective activities from Xylaria nigripes
Fig. 2. Key 2D NMR correlations of compounds 1–5.
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International Brain Laboratory public data
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