Works matching DE "GINSENOSIDES"
Results: 1253
Protocol for efficient ginseng transformation.
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- Plant Cell, Tissue & Organ Culture, 2023, v. 153, n. 2, p. 429, doi. 10.1007/s11240-023-02465-y
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- Article
Linalool as a novel natural factor enhancing ginsenoside production in hairy root cultures of American ginseng.
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- Plant Cell, Tissue & Organ Culture, 2023, v. 153, n. 2, p. 285, doi. 10.1007/s11240-023-02456-z
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Micropropagation of Lang Bian ginseng: an endemic medicinal plant.
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- Plant Cell, Tissue & Organ Culture, 2022, v. 151, n. 3, p. 565, doi. 10.1007/s11240-022-02372-8
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- Article
Abscisic acid is required for cold-induced accumulation of ginsenosides Rg<sub>1</sub> and Re in Panax ginseng adventitious roots.
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- Plant Cell, Tissue & Organ Culture, 2022, v. 149, n. 1/2, p. 325, doi. 10.1007/s11240-021-02222-z
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A plant-transformation-competent BIBAC library of ginseng ( Panax ginseng C. A. Meyer) for functional genomics research and characterization of genes involved in ginsenoside biosynthesis.
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- Molecular Breeding, 2013, v. 31, n. 3, p. 685, doi. 10.1007/s11032-012-9826-4
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Isolation, characterisation and genome analysis of a novel ginsenosides hydrolysing bacterium Ginsengibacter hankyongi gen. nov., sp. nov. isolated from soil.
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- Antonie van Leeuwenhoek, 2021, v. 114, n. 1, p. 11, doi. 10.1007/s10482-020-01485-4
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Efficient biotransformation of ginsenoside Rb to Rd by isolated Aspergillus versicolor, excreting β-glucosidase in the spore production phase of solid culture.
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- Antonie van Leeuwenhoek, 2015, v. 108, n. 5, p. 1117, doi. 10.1007/s10482-015-0565-5
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- Article
Microbial ketonization of ginsenosides F1 and C-K by Lactobacillus brevis.
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- Antonie van Leeuwenhoek, 2014, v. 106, n. 6, p. 1215, doi. 10.1007/s10482-014-0291-4
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- Article
Isolation and characterization of novel ginsenoside-hydrolyzing glycosidase from Microbacterium esteraromaticum that transforms ginsenoside Rb2 to rare ginsenoside 20( S)-Rg3.
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- Antonie van Leeuwenhoek, 2013, v. 104, n. 1, p. 129, doi. 10.1007/s10482-013-9933-1
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Sphingomonas ginsenosidivorax sp. nov., with the ability to transform ginsenosides.
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- Antonie van Leeuwenhoek, 2013, v. 103, n. 6, p. 1359, doi. 10.1007/s10482-013-9916-2
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Nocardioides panaciterrulae sp. nov., isolated from soil of a ginseng field, with ginsenoside converting activity.
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- Antonie van Leeuwenhoek, 2013, v. 103, n. 6, p. 1385, doi. 10.1007/s10482-013-9919-z
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- Article
Lactobacillus ginsenosidimutans sp. nov., isolated from kimchi with the ability to transform ginsenosides.
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- Antonie van Leeuwenhoek, 2013, v. 103, n. 4, p. 867, doi. 10.1007/s10482-012-9868-y
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- Article
Bioconversion of ginsenoside Rc into Rd by a novel α- l-arabinofuranosidase, Abf22-3 from Leuconostoc sp. 22-3: cloning, expression, and enzyme characterization.
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- Antonie van Leeuwenhoek, 2013, v. 103, n. 4, p. 747, doi. 10.1007/s10482-012-9856-2
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- Article
A New Alcohol Glycoside from the Leaves of Panax vietnamensis.
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- Chemistry of Natural Compounds, 2025, v. 61, n. 1, p. 5, doi. 10.1007/s10600-025-04563-z
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Chemical Constituents from the Leaves of Camellia ptilosperma and their Cytotoxicity.
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- Chemistry of Natural Compounds, 2024, v. 60, n. 4, p. 790, doi. 10.1007/s10600-024-04446-9
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Preparation and Vasodilatory Activity of Rare Ginsenosides.
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- Chemistry of Natural Compounds, 2018, v. 54, n. 6, p. 1182, doi. 10.1007/s10600-018-2589-3
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New Triterpenoid Saponin C-20 Epimers from the Alkaline-Degradation Products of Ginsenoside Re and Their Cytotoxic Activities.
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- Chemistry of Natural Compounds, 2018, v. 54, n. 3, p. 490, doi. 10.1007/s10600-018-2386-z
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- Article
Biotransformation of Ginsenosides Re and Rg into Rg and Rh by Thermostable β-Glucosidase from Thermotoga thermarum.
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- Chemistry of Natural Compounds, 2017, v. 53, n. 3, p. 472, doi. 10.1007/s10600-017-2025-0
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Characterization of Three Oleane-Type Saponins from Panax ginseng.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 6, p. 1193, doi. 10.1007/s10600-015-1530-2
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Biotransformation of Ginsenosides Re and Rg by the Bacterium Microbacterium sp. GT35.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 1, p. 81, doi. 10.1007/s10600-015-1208-9
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Structure of Acid Hydrolysate of Total Ginsenosides and Their Cytotoxic Activity.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 4, p. 687, doi. 10.1007/s10600-014-1053-2
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- Article
Biotransformation of the Principal Ginsenosides of Panax ginseng Into Minor Glycosides Through the Action of Bacterium Paenibacillus sp. BG134.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 4, p. 691, doi. 10.1007/s10600-014-1054-1
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Biotransformation of Ginsenoside Rc into C-Mc by the Bacterium Sphingopyxis sp. BG97.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 3, p. 565, doi. 10.1007/s10600-014-1019-4
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Transformation of Ginsenoside Rc into (20 S)-Rg by the Bacterium Leuconostoc sp. BG78.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 3, p. 562, doi. 10.1007/s10600-014-1018-5
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Biotransformation of Ginsenoside Rd into 20( S)-Rg by Bacterium Flavobacterium sp. BGS36.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 1, p. 181, doi. 10.1007/s10600-014-0907-y
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Biotransformation of ginsenoside Rb into F-2 and compound K by bacterium Sphingomonas sp. BG 25.
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- Chemistry of Natural Compounds, 2014, v. 49, n. 6, p. 1168, doi. 10.1007/s10600-014-0853-8
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Three New Ginsenosides from the Heat-Processed Roots of <i>Panax ginseng</i>.
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- Chemistry of Natural Compounds, 2013, v. 49, n. 5, p. 882, doi. 10.1007/s10600-013-0769-8
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Biotransformation of Ginsenoside Rb into Rd by the Bacterium Lysobacter panaciterrae.
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- Chemistry of Natural Compounds, 2013, v. 49, n. 4, p. 773, doi. 10.1007/s10600-013-0740-8
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Anti-colon carcinoma cell activity of ginsenosides from the acid hydrolysate of Panax ginseng.
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- Chemistry of Natural Compounds, 2013, v. 48, n. 6, p. 1017, doi. 10.1007/s10600-013-0453-z
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- Article
The production of ginsenosides in hairy root cultures of American Ginseng, Panax quinquefolium L. and their antimicrobial activity.
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- In Vitro Cellular & Developmental Biology Plant, 2013, v. 49, n. 1, p. 24, doi. 10.1007/s11627-012-9469-5
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Tandem Mass Spectrometry for the Analysis of Ginsenosides in a Phytoadaptogene Composition with Antitumor Properties.
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- Theoretical Foundations of Chemical Engineering, 2021, v. 55, n. 6, p. 1246, doi. 10.1134/S0040579521050225
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Ginsenoside Rb1 Alleviates Lipopolysaccharide-Induced Inflammatory Injury by Downregulating miR-222 in WI-38 Cells.
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- Cell Transplantation, 2021, v. 30, p. 1, doi. 10.1177/09636897211002787
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- Article
人参皂苷Rg2通过PI3K/AKT/NF-kB信号通路减轻 LPS诱导的RAW264.7细胞炎症.
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- Modern Food Science & Technology, 2024, v. 40, n. 12, p. 1, doi. 10.13982/j.mfst.1673-9078.2024.12.0016
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- Article
人参皂苷Rg3对氧化应激诱导神经细胞损伤的保护作用.
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- Modern Food Science & Technology, 2024, v. 40, n. 8, p. 116, doi. 10.13982/j.mfst.1673-9078.2024.8.0693
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- Article
热转化西洋参茎叶皂苷的抗氧化及美白活性.
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- Modern Food Science & Technology, 2022, v. 38, n. 9, p. 254, doi. 10.13982/j.mfst.1673-9078.2022.9.1285
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- Article
Modulation of T-Bet and GATA-3 expression in experimental autoimmune thyroiditis rats through ginsenoside treatment.
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- Endocrine Research, 2016, v. 41, n. 1, p. 28, doi. 10.3109/07435800.2015.1066800
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- Article
Hepatoprotective effect of ginsenoside Rg1 from Panax ginseng on carbon tetrachloride‐induced acute liver injury by activating Nrf2 signaling pathway in mice.
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- Environmental Toxicology, 2018, v. 33, n. 10, p. 1050, doi. 10.1002/tox.22616
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Oxidative stresses-mediated apoptotic effects of ginsenoside Rb1 on pre- and post-implantation mouse embryos in vitro and in vivo.
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- Environmental Toxicology, 2017, v. 32, n. 8, p. 1990, doi. 10.1002/tox.22366
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Impairment of preimplantation and postimplantation embryonic development through intrinsic apoptotic processes by ginsenoside Rg1 in vitro and in vivo.
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- Environmental Toxicology, 2017, v. 32, n. 7, p. 1937, doi. 10.1002/tox.22416
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- Article
人参皂苷 Rg1 通过 Wnt3a/茁-catenin 信号通路影响糖尿病大鼠肾损伤的 机制研究.
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- Progress in Modern Biomedicine, 2023, v. 23, n. 17, p. 3216, doi. 10.13241/j.cnki.pmb.2023.17.003
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人参皂苷 Rg1 对抑郁症大鼠抑郁行为和海马神经元损伤、 PKA、PKC 的影响.
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- Progress in Modern Biomedicine, 2023, v. 23, n. 16, p. 3027, doi. 10.13241/j.cnki.pmb.2023.16.005
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人参皂苷 Rh2 对大鼠 C6 胶质瘤细胞 Siah-1、Synaptophysin、MMP9 及 VEGF 表达的影响.
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- Progress in Modern Biomedicine, 2023, v. 23, n. 13, p. 2419, doi. 10.13241/j.cnki.pmb.2023.13.004
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人参皂苷 Rg3 通过调节自噬减轻脓毒症心肌损伤.
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- Progress in Modern Biomedicine, 2022, v. 22, n. 8, p. 1419, doi. 10.13241/j.cnki.pmb.2022.08.004
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- Article
Intricate microbe‐plant‐metabolic remodeling mediated by intercropping enhances the quality of Panax quinquefolius L.
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- Physiologia Plantarum, 2024, v. 176, n. 5, p. 1, doi. 10.1111/ppl.14499
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- Article
The Phytophthora cactorum genome provides insights into the adaptation to host defense compounds and fungicides.
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- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-24939-2
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- Article
The Synthesis of Ginsenoside Compound K Using a Surface-Displayed β-Glycosidase Whole-Cell Catalyst.
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- Catalysts (2073-4344), 2023, v. 13, n. 10, p. 1375, doi. 10.3390/catal13101375
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A Novel Ginsenoside-Transforming α-L-Rhamnosidase from Bifidobacterium : Screening, Characterization and Application.
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- Biomolecules (2218-273X), 2024, v. 14, n. 12, p. 1611, doi. 10.3390/biom14121611
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- Article
So Shiho Tang Reduces Inflammation in Lipopolysaccharide-Induced RAW 264.7 Macrophages and Dextran Sodium Sulfate-Induced Colitis Mice.
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- Biomolecules (2218-273X), 2024, v. 14, n. 4, p. 451, doi. 10.3390/biom14040451
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- Article
The AP2/ERF Transcription Factor PgERF120 Regulates Ginsenoside Biosynthesis in Ginseng.
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- Biomolecules (2218-273X), 2024, v. 14, n. 3, p. 345, doi. 10.3390/biom14030345
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- Article
Ginsenoside and Its Therapeutic Potential for Cognitive Impairment.
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- Biomolecules (2218-273X), 2022, v. 12, n. 9, p. 1310, doi. 10.3390/biom12091310
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- Article