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965 results for “Artemisia”

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zenodo32/100

Fig. 5 in Artemidubolides A T, cytotoxic unreported guaiane-type sesquiterpenoid dimers against three hepatoma cell lines from Artemisia dubia

Fig. 5. The Experimental and calculated ECD spectra of compounds 3, 5, 7, 8, 10, 12, 13, 14, 16, 17, and 19.

opennotspecifiedOct 2022View details →
zenodo32/100

Fig. 8. Compound 4 in Artemidubolides A T, cytotoxic unreported guaiane-type sesquiterpenoid dimers against three hepatoma cell lines from Artemisia dubia

Fig. 8. Compound 4 inhibited migration and invasion of HepG2 cells. HepG2 cells were treated with different concentrations (0.0, 3.5, 7.0 and 10.5 μM) of 4 for 48 h. (A) Representative photographs of the Transwell assay showed migrated and invaded cells after incubation. (B) Histogram of migrated and invaded cells after incubation. *P <0.05, **P <0.01, and ***P <0.001, n = 3.

opennotspecifiedOct 2022View details →
zenodo32/100

Fig. 7 in Artemidubolides A T, cytotoxic unreported guaiane-type sesquiterpenoid dimers against three hepatoma cell lines from Artemisia dubia

Fig. 7. Cytotoxic activity of different fractions of A.dubia against HepG2 (100.0 μg/mL). Data were expressed as means ± SD (n = 3). Sorafenib with an IC50 value of 14.6 ± 0.4 μM was used as the positive control.

opennotspecifiedOct 2022View details →
zenodo32/100

Fig. 5 in Biotransformation of artemisinic acid to bioactive derivatives by endophytic Penicillium oxalicum B4 from Artemisia annua L.

Fig. 5. Time course for the biotransformation of artemisinic acid (AA) by Penicillium oxalicum B4. AA (3.50 mg/50 mL) was added to 2-day-old culture for the biotransformation.

opennotspecifiedMay 2021View details →
zenodo32/100

Fig. 4 in Biotransformation of artemisinic acid to bioactive derivatives by endophytic Penicillium oxalicum B4 from Artemisia annua L.

Fig. 4. Time course of mycelial biomass (A) and the biotransformation of artemisinic acid (AA) by Penicillium oxalicum B4. AA (3.50 mg/50 mL) was added to 2-day-old culture for the biotransformation. Data presented are the means ± SD of results from three independent experiments.

opennotspecifiedMay 2021View details →
zenodo32/100

Fig. 7 in Biotransformation of artemisinic acid to bioactive derivatives by endophytic Penicillium oxalicum B4 from Artemisia annua L.

Fig. 7. Inhibitory effects of metabolite 4 (A) and 7 (B) on cell viability and LPSinduced nitrite production in RAW 264.7 cells. Normal cells were incubated for 24 h with metabolite 4 and 7 at indicated concentrations. Cells were pretreated with the indicated concentrations of metabolite 4 and 7 for 1 h followed by treatment with LPS (1.0 μg/mL). After 24 h of incubation, the amount of nitrite in the culture supernatants and cell viability were measured. Data presented are the means ± SD of results from three independent experiments (###p <0.001 versus untreated group; *p <0.05, **p <0.01 versus LPS treated group. The small letters indicate the significant difference (p <0.05) between groups).

opennotspecifiedMay 2021View details →
zenodo32/100

Fig. 8. Compound 4 inhibited IL-1 in Guaianolides from Artemisia codonocephala suppress interleukine-1β secretion in macrophages

Fig. 8. Compound 4 inhibited IL-1β production in THP-1 macrophages. (A) Immunofluorescence staining of IL-1β was performed. Scale bar = 10 μm. (B) The protein level of IL-1β in the culture medium from THP-1 cells was determined by ELISA. (C) Cleaved IL- 1β, NLRP3 and Caspase 1 in the supernatant or lysates of THP-1 cells were detected by western blotting. GAPDH was used as an internal loading control. (D) Expression of autophagy related proteins were detected by Western blotting. GAPDH was used as an internal loading control. (E) Expression of autophagy related proteins in THP-1 cells treated with or without 10 μM compound 4 and 5 mM 3-MA. GAPDH was used as an internal loading control. (F) mRFP- GFP-LC3 puncta were measured using a confocal microscope. Scale bar = 5 μm. (G) The levels of IL-1β in the culture medium from THP-1 cells treated with or without 10 μM compound 4 and 5 mM 3-MA. Data are expressed as means ± SD (n = 6). ###P <0.001, LPS + ATP vs. control, **P <0.01 and ***P <0.001, 4 vs. LPS + ATP.

opennotspecifiedDec 2021View details →
zenodo32/100

Fig. 7 in Guaianolides from Artemisia codonocephala suppress interleukine-1β secretion in macrophages

Fig. 7. The HPLC-HRESIMS result (1–11min) of the acetone extract and the identification of the undescribed compounds of Artemisia codonocephala.

opennotspecifiedDec 2021View details →
ClinicalTrials.gov32/100

Efficacy of Artemisia Pollen Specific Allergen Immunotherapy

ClinicalTrials.gov study NCT05318157. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

Evaluation of Artemisia Annua and Moringa

ClinicalTrials.gov study NCT03366922. IPD Sharing: NO. Countries: 1. Publications: 4.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Camostat and Artemisia Annua vs Placebo in COVID-19 Outpatients

ClinicalTrials.gov study NCT04530617. IPD Sharing: NO. Countries: 1. Publications: 29.

closedIPD-NOFeb 2026View details →
dryad32/100

An insect-pollinated species in a wind-pollinated genus: case study of the endemic plant, Laramie chickensage (Artemisia simplex)

Open the record for dataset details and reuse information.

publicSep 2022View details →
dryad32/100

Data from: Climate drives adaptive genetic responses associated with survival in big sagebrush (Artemisia tridentata)

Open the record for dataset details and reuse information.

publicMar 2016View details →
dryad32/100

Data from: Nitrogen addition pulse has minimal effect in big sagebrush (Artemisia tridentata) communities on the Pinedale Anticline, Wyoming (USA)

Open the record for dataset details and reuse information.

publicJun 2019View details →
dryad32/100

Data from: Root vertical distributions of two Artemisia species and their relationships with soil resources in the Hunshandake desert, China

Open the record for dataset details and reuse information.

publicMar 2020View details →
dryad32/100

Data from: Deep sequencing of amplicons reveals widespread intraspecific hybridization and multiple origins of polyploidy in big sagebrush (Artemisia tridentata)

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publicFeb 2013View details →
dryad32/100

Data from: Artemisia baxoiensis (Asteraceae: Anthemideae), a distinctive new species from Xizang, China

Open the record for dataset details and reuse information.

publicJul 2019View details →
zenodo28/100

Figure 1 from: Hrytsyk RA, Kutsyk RV, Yurchyshyn OI, Struk ОА, Kireev IV, Grytsyk AR (2021) The investigation of antimicrobial and antifungal activity of some Artemisia L. species. Pharmacia 68(1): 93-100. https://doi.org/10.3897/pharmacia.68.e47521

Figure 1 Antimicrobial activity of Artemisia absinthium L., Artemisia vulgaris L., Artemisia abrotanum L. extracts in relation to the test cultures of microorganisms: АEsherichia coli, BStaphylococcus epidermidis, CCandida tropicalis, DAspergillus niger, EEnterococcus faecalis, FStaphylococcus aureus

opencc-by-4.0Jan 2021View details →
zenodo28/100

FIGURE 2 in Artemisia taibaishanensis (Asteraceae, Anthemideae), a new synonym of A. qinlingensis from China

FIGURE 2. Paratype sheets of Artemisia qinlingensis.

opennotspecifiedFeb 2021View details →
zenodo28/100

FIGURE 1 in Artemisia taibaishanensis (Asteraceae, Anthemideae), a new synonym of A. qinlingensis from China

FIGURE 1. Lectotype (A) and isolectotype (B–D) sheets of Artemisia qinlingensis.

opennotspecifiedFeb 2021View details →

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International Brain Laboratory public data

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Last verified 2026-04-29Open record