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    <responseDate>2026-10-12T05:28:13Z</responseDate>
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    <identifier>10.57760/sciencedb.36081</identifier>
    <datestamp>2026-07-16T09:48:09Z</datestamp>
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  <dc:date>2026-07-16</dc:date>
  <dc:title>Efficacy of docetaxel against Toxoplasma gondii in vitro</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.36081</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Fresh RH tachyzoites (approximately 2&amp;times;107&amp;nbsp;parasites) were incubated with docetaxel (5 nM) or 0.1%&amp;nbsp;DMSO (vehicle) for 12 h at 4 ℃. Total RNA was extracted using TRIzol (Thermo Fisher Scientific, USA) according to the manufacturer&amp;rsquo;s protocol. RNA quality was determined using an Agilent 2100 bioanalyzer (Agilent Technologies, Santa Clara, CA). RNA-Library preparation and sequencing were conducted by Novogene (Beijing, China).&amp;nbsp;Sequencing was performed using the Illumina platform (Illumina, San Diego, CA, USA). Clean reads were aligned to the T. gondii&amp;nbsp;reference genome (GenBank accession number: PRJNA28893) using HISAT2 software. We used the DESeq to perform differentially expressed gene (DEG) analysis (P-value &amp;lt; 0.05). GO enrichment analysis of differentially expressed genes was implemented by the cluster Profiler R package, in which gene length bias was corrected (Yu et al., 2012). GO terms with corrected P-value &amp;lt; 0.05 were considered significantly enriched by differential expressed genes. We used cluster Profiler R package to test the statistical enrichment of differential expression genes in KEGG pathways.</dc:description>
  <dc:subject>Toxoplasma gondii; docetaxel; GO enrichment; KEGG pathways</dc:subject>
  <dc:creator>Chun-Xue Zhou</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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