<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9</volume><submitter>Li X</submitter><pubmed_abstract>Although multiple bioactive components have been identified in Fufang E'jiao Jiang (FEJ), their hematopoietic effects and molecular mode of action &lt;i>in vivo&lt;/i> are still not fully understood. In the current study, we analyzed the effects of martynoside, R-notoginsenoside R2 (R2), and 20S-ginsenoside Rg2 (Rg2) in a 5-fluorouracil-induced myelosuppression mouse model. Bone marrow nucleated cells (BMNCs) counts, hematopoietic progenitor cell colony-forming unit (CFU) assay, as well as flow cytometry analysis of Lin&lt;sup>-&lt;/sup>/c-kit&lt;sup>+&lt;/sup>/Sca-1&lt;sup>+&lt;/sup> hematopoietic stem cell (HSC) population were conducted, and bone marrow cells were subjected to RNA sequencing. The transcriptome data were processed based on the differentially expressed genes. The results of the analysis show tha</pubmed_abstract><journal>Frontiers in pharmacology</journal><pagination>616</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6008481</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Transcriptome Profiling Analysis Reveals the Potential Mechanisms of Three Bioactive Ingredients of Fufang E'jiao Jiang During Chemotherapy-Induced Myelosuppression in Mice.</pubmed_title><pmcid>PMC6008481</pmcid><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Qian J</pubmed_authors><pubmed_authors>Gong S</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Hong Z</pubmed_authors><pubmed_authors>Qu H</pubmed_authors><pubmed_authors>Zhou X</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors><pubmed_authors>Liu W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcriptome Profiling Analysis Reveals the Potential Mechanisms of Three Bioactive Ingredients of Fufang E'jiao Jiang During Chemotherapy-Induced Myelosuppression in Mice.</name><description>Although multiple bioactive components have been identified in Fufang E'jiao Jiang (FEJ), their hematopoietic effects and molecular mode of action &lt;i>in vivo&lt;/i> are still not fully understood. In the current study, we analyzed the effects of martynoside, R-notoginsenoside R2 (R2), and 20S-ginsenoside Rg2 (Rg2) in a 5-fluorouracil-induced myelosuppression mouse model. Bone marrow nucleated cells (BMNCs) counts, hematopoietic progenitor cell colony-forming unit (CFU) assay, as well as flow cytometry analysis of Lin&lt;sup>-&lt;/sup>/c-kit&lt;sup>+&lt;/sup>/Sca-1&lt;sup>+&lt;/sup> hematopoietic stem cell (HSC) population were conducted, and bone marrow cells were subjected to RNA sequencing. The transcriptome data were processed based on the differentially expressed genes. The results of the analysis show tha</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2026-05-03T17:32:57.567Z</modification><creation>2019-03-26T23:43:39Z</creation></dates><accession>S-EPMC6008481</accession><cross_references><pubmed>29950993</pubmed><doi>10.3389/fphar.2018.00616</doi></cross_references></HashMap>