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295 results for “Daphne”
Figure 6 from: Loni A, Samartsev KG, Scaramozzino PL, Belokobylskij SA, Lucchi A (2016) Braconinae parasitoids (Hymenoptera, Braconidae) emerged from larvae of Lobesia botrana (Denis & Schiffermüller) (Lepidoptera, Tortricidae) feeding on Daphne gnidium L. ZooKeys 587: 125-150. https://doi.org/10.3897/zookeys.587.8478
Figure 6 - Habrobracon concolorans (Marshall, 1900), female. A Body, dorsal view B Wings C Head and mesonotum, dorsal view D Head, sub-lateral view E Head, front view F Propodeum and metasoma, dorsal view G Metasoma, dorsal view.
Figure 7 from: Loni A, Samartsev KG, Scaramozzino PL, Belokobylskij SA, Lucchi A (2016) Braconinae parasitoids (Hymenoptera, Braconidae) emerged from larvae of Lobesia botrana (Denis & Schiffermüller) (Lepidoptera, Tortricidae) feeding on Daphne gnidium L. ZooKeys 587: 125-150. https://doi.org/10.3897/zookeys.587.8478
Figure 7 - Habrobracon hebetor Say, 1936, female, A Wings B Head and mesosoma, lateral view C Head, front view D Head, dorsal view E Mesosoma, dorsal view F Metasoma, dorsal view.
Figure 3 from: Loni A, Samartsev KG, Scaramozzino PL, Belokobylskij SA, Lucchi A (2016) Braconinae parasitoids (Hymenoptera, Braconidae) emerged from larvae of Lobesia botrana (Denis & Schiffermüller) (Lepidoptera, Tortricidae) feeding on Daphne gnidium L. ZooKeys 587: 125-150. https://doi.org/10.3897/zookeys.587.8478
Figure 3 - Sprouts of Daphne gnidium infested by moth larvae. A Field situation B Nests stored in vials until emergence of the moth or the parasitoid.
Figure 1 from: Loni A, Samartsev KG, Scaramozzino PL, Belokobylskij SA, Lucchi A (2016) Braconinae parasitoids (Hymenoptera, Braconidae) emerged from larvae of Lobesia botrana (Denis & Schiffermüller) (Lepidoptera, Tortricidae) feeding on Daphne gnidium L. ZooKeys 587: 125-150. https://doi.org/10.3897/zookeys.587.8478
Figure 1 - Natural Reserve of San Rossore (Pisa): different habitats of the experimental area. A Landscape B Fore dune close to sandy shores C vegetation of established dunes D Wooded area with holm oak. White arrows indicate plants of Dapne gnidium.
Fig. 6. X in Guide isolation of guaiane-type sesquiterpenoids from Daphne tangutica maxim. And their anti-inflammatory activities
Fig. 6. X-ray structure of compounds 1, 8, 9 and 24.
Fig. 5 in Guide isolation of guaiane-type sesquiterpenoids from Daphne tangutica maxim. And their anti-inflammatory activities
Fig. 5. Key NOESY correlations of undescribed compounds 1-13.
Fig. 7. Experimental and calculated ECD spectra compounds 1-13 in Guide isolation of guaiane-type sesquiterpenoids from Daphne tangutica maxim. And their anti-inflammatory activities
Fig. 7. Experimental and calculated ECD spectra compounds 1-13.
Fig. 3 in Guide isolation of guaiane-type sesquiterpenoids from Daphne tangutica maxim. And their anti-inflammatory activities
Fig. 3. Chemical structure of compounds 1-32.
Fig. 1 in Guide isolation of guaiane-type sesquiterpenoids from Daphne tangutica maxim. And their anti-inflammatory activities
Fig. 1. Clusters from the molecular network of the all subfractions of D. tangutica.
Fig. 2 in Guided isolation of daphnane-type diterpenes from Daphne genkwa by molecular network strategies
Fig. 2. The structures of compounds 1–12.
Fig. 5 in Guided isolation of daphnane-type diterpenes from Daphne genkwa by molecular network strategies
Fig. 5. Key NOESY correlations of compounds 1, 2, 4, and 5.
Fig. 4. Key 1H–1H in Guided isolation of daphnane-type diterpenes from Daphne genkwa by molecular network strategies
Fig. 4. Key 1H–1H COSY, HMBC correlations of compounds 1, 2, 4, and 5.
Fig. 3 in Sesquiterpenoids from the roots of Daphne genkwa Siebold et Zucc. With potential anti-inflammatory activity
Fig. 3. Key NOESY correlations of compounds 1–3.
Fig. 5 in Sesquiterpenoids from the roots of Daphne genkwa Siebold et Zucc. With potential anti-inflammatory activity
Fig. 5. Experimental and calculated ECD spectra of compounds 5 and 6.
Fig. 1 in Sesquiterpenoids from the roots of Daphne genkwa Siebold et Zucc. With potential anti-inflammatory activity
Fig. 1. Chemical structures of 1–9.
Fig. 7 in Sesquiterpenoids from the roots of Daphne genkwa Siebold et Zucc. With potential anti-inflammatory activity
Fig. 7. Inhibition against LPS-induced NO production in RAW264.7 macrophages.
Fig. 4 in Sesquiterpenoids from the roots of Daphne genkwa Siebold et Zucc. With potential anti-inflammatory activity
Fig. 4. Experimental and calculated ECD spectra of compounds 1–4.
Fig. 14 in Daphne giraldii Nitsche (Thymelaeaceae): Phytochemistry, pharmacology and medicinal uses
Fig. 14. Concerted summary of SAR studies of flavans.
Fig. 13 in Daphne giraldii Nitsche (Thymelaeaceae): Phytochemistry, pharmacology and medicinal uses
Fig. 13. SAR studies of flavans selectively inhibiting Hep3B cell.
Fig. 7. Other compounds isolated from D in Daphne giraldii Nitsche (Thymelaeaceae): Phytochemistry, pharmacology and medicinal uses
Fig. 7. Other compounds isolated from D. giraldii.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.