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61 results for “Panax”
FIGURE 3. Alternaria hedjaroudei. a–c in Morphological and molecular identification of Alternaria hedjaroudei sp. nov., a new species in section Panax from Iran
FIGURE 3. Alternaria hedjaroudei. a–c, Ascomata formed on PCA culture medium. d–e, Ascomata wall. f–g, Hymenium. h–j, 8-spored mature asci. k, Pseudoparaphyses. l–z, Ascospores. Scale bars 20 µm.
FIGURE 2. Alternaria hedjaroudei. a-d, Colonies after 7 in Morphological and molecular identification of Alternaria hedjaroudei sp. nov., a new species in section Panax from Iran
FIGURE 2. Alternaria hedjaroudei. a-d, Colonies after 7 days on PDA (a), PCA (b), HA (c), and V8–A (d). e–f, Sporulation pattern. g–l, Primary conidiophores. m–o, Secondary conidiophores. p–z, Conidia. Scale bars 25 µm.
Fig. 5 in Molecular differentiation of Panax notoginseng grown under different conditions by internal extractive electrospray ionization mass spectrometry and multivariate analysis
Fig. 5. Multivariate statistical analysis results of 9 different types of Panax notoginseng samples. (a) Score scatter plot of 2D PCA model, (b) Score scatter plot of 3D PCA model, (c) Score scatter plot of OPLS-DA model, (d) Bar plot with OPLS-DA model of VIP.
Fig. 4 in Molecular differentiation of Panax notoginseng grown under different conditions by internal extractive electrospray ionization mass spectrometry and multivariate analysis
Fig. 4. Tandem MS analysis of characteristic ions in Panax notoginseng samples. (a) MS3 spectrum of m/z 1143 → 1107→, (b) MS3 spectrum of m/z 1193 → 1149→, (c) MS3 spectrum of m/z 885 → 841, (d) MS3 spectrum of m/z 1031 → 987, (e) MS3 spectrum of m/z 1245 → 1209, (f) MS3 spectrum of m/z 968 → 931.
Fig. 3 in Molecular differentiation of Panax notoginseng grown under different conditions by internal extractive electrospray ionization mass spectrometry and multivariate analysis
Fig. 3. Mass spectra of different types of Panax notoginseng samples analyzed by iEESI-MS. (a) Mass spectrum of Panax notoginseng from Kunming, (b) Mass spectrum of Panax notoginseng from Qujing, (c) Mass spectrum of Panax notoginseng from Hongjiaozhou, (d) Mass spectrum of Panax notoginseng from Wenshan (1 year), (e) Mass spectrum of Panax notoginseng from Wenshan (2 year), (f) Mass spectrum of Panax notoginseng from Wenshan (3 year), (g) Mass spectrum of Panax notoginseng from Hongjiaozhou (black soil), (h) Mass spectrum of Panax notoginseng from Hongjiaozhou (white soil), (i) Mass spectrum of Panax notoginseng from Hongjiaozhou (red soil). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2 in Molecular differentiation of Panax notoginseng grown under different conditions by internal extractive electrospray ionization mass spectrometry and multivariate analysis
Fig. 2. Chemical structures of eight ginsenosides used in this study as reference standards. G, ginsenoside; NG, notoginsenoside; glc, glucoside; rha, rhamnoside; xyl, xyloside; ara, arabinoside.
Fig. 1 in Molecular differentiation of Panax notoginseng grown under different conditions by internal extractive electrospray ionization mass spectrometry and multivariate analysis
Fig. 1. Schematic illustration of iEESI-MS for direct analysis of Panax notoginseng samples. (a) Analytical procedure of Panax notoginseng analysis by iEESI-MS. Approximately 0.1 mg of Panax notoginseng tissue was loaded into the sample chamber by punching without sample pretreatment, (b) Disposable iEESI device and its components, (c) Photo of iEESI-MS interface.
Effects of Panax Ginseng and Salvia Miltiorrhiza Supplementation on Vascular Function
ClinicalTrials.gov study NCT02007304. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Data from: Demographic stimulation of the obligate understorey herb, Panax quinquefolius L., in response to natural forest canopy disturbances
Open the record for dataset details and reuse information.
FIGURE 2 in A new variety of Panax (Araliaceae) from Lam Vien Plateau, Vietnam and its molecular evidence
FIGURE 2. Neighbor-joining phylogenetic tree among ten investigated taxa.
Figure 3 from: Linh NN, Hang PLB, Hue HTT, Ha NH, Hanh HH, Ton ND, Hien LTT (2022) Species discrimination of novel chloroplast DNA barcodes and their application for identification of Panax (Aralioideae, Araliaceae). PhytoKeys 188: 1-18. https://doi.org/10.3897/phytokeys.188.75937
Figure 3 Successful identification rates among analyzed barcodes by Best Match and Best Close Match function.
Figure 2 from: Linh NN, Hang PLB, Hue HTT, Ha NH, Hanh HH, Ton ND, Hien LTT (2022) Species discrimination of novel chloroplast DNA barcodes and their application for identification of Panax (Aralioideae, Araliaceae). PhytoKeys 188: 1-18. https://doi.org/10.3897/phytokeys.188.75937
Figure 2 Percent relative abundance in distribution of intra/interspecific K2P pairwise distances estimated for markers.
Figure 5 from: Linh NN, Hang PLB, Hue HTT, Ha NH, Hanh HH, Ton ND, Hien LTT (2022) Species discrimination of novel chloroplast DNA barcodes and their application for identification of Panax (Aralioideae, Araliaceae). PhytoKeys 188: 1-18. https://doi.org/10.3897/phytokeys.188.75937
Figure 5 Percentage of variable sites, mean pairwise distances, and correct classification percentages of all markers and combinations
Figure 4 from: Linh NN, Hang PLB, Hue HTT, Ha NH, Hanh HH, Ton ND, Hien LTT (2022) Species discrimination of novel chloroplast DNA barcodes and their application for identification of Panax (Aralioideae, Araliaceae). PhytoKeys 188: 1-18. https://doi.org/10.3897/phytokeys.188.75937
Figure 4 Results of mPTP species delimitation analysis for several markers based on ML trees A Species delimitation for marker trnQ-rps16B Species delimitation for the combination of markers 1+3+4. Bootstrap values are displayed on the branches. The red branches represent supported species delimitations. Sequences highlighted in orange originate from this study.
Figure 1 from: Linh NN, Hang PLB, Hue HTT, Ha NH, Hanh HH, Ton ND, Hien LTT (2022) Species discrimination of novel chloroplast DNA barcodes and their application for identification of Panax (Aralioideae, Araliaceae). PhytoKeys 188: 1-18. https://doi.org/10.3897/phytokeys.188.75937
Figure 1 Distribution of Panax in Vietnam and sample locations. P. vietnamensis (green) collected in Quang Nam and Kon Tum Provinces. P. vietnamensis var. fuscidiscus (brown) collected in Lai Chau Province. Panax sp. Puxailaileng (pink) collected in Nghe An Province. P. bipinnatifidus (blue) and P. stipuleanatus (yellow) collected in Lao Cai Province. The natural distribution of P. vietnamensis, P. vietnamensis var. fuscidiscus, and Panax sp. are marked as green, brown, and pink, respectively. The wild habitat for P. bipinnatifidus and P. stipuleanatus is shown in yellow, and the purple area represents the distribution region of P. vietnamensis var. langbiangensis (not included in this study).
FIGURE 1 in A new variety of Panax (Araliaceae) from Lam Vien Plateau, Vietnam and its molecular evidence
FIGURE 1. Maximum likelihood phylogenetic tree among ten investigated taxa.
Clinical Study on the Treatment of Hypertensive Intracerebral Hemorrhage With Panax Notoginseng Saponin
ClinicalTrials.gov study NCT02999048. IPD Sharing: Not stated. Countries: 0. Publications: 13.
Effect of Panax Ginseng on the Cognitive Performance in Alzheimer's Disease
ClinicalTrials.gov study NCT00391833. IPD Sharing: Not stated. Countries: 0. Publications: 1.
Data from: Karyotype analysis of Panax ginseng C.A. Meyer, 1843 (Araliaceae) based on rDNA loci and DAPI band distribution
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Phased secondary small interfering RNAs in Panax notoginseng
GEO Series GSE98118. Panax notoginseng. 7 samples. Type: Non-coding RNA profiling by high throughput sequencing.
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