5 research outputs found

    Distribution of the <i>MTHFR</i> genotypes among 266 childhood ALL patients and 266 controls.

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    <p><sup>a</sup> Based on Pearson’s chi-square test</p><p><sup>b</sup> OR: odds ratio; CI: confidence interval</p><p>* Statistically significant</p><p>Distribution of the <i>MTHFR</i> genotypes among 266 childhood ALL patients and 266 controls.</p

    Distribution of the <i>MTHFR</i> C677T and A1298C genotypes stratified by age and gender

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    <p><sup>a</sup><i>P</i> for trend based on chi-square test.</p><p><sup>b</sup><i>P</i> for interaction based on likelihood ratio test; NS, non-significant.</p><p><sup>c</sup> OR, odds ratio; CI, confidence interval.</p><p>* Statistically significant.</p><p>Distribution of the <i>MTHFR</i> C677T and A1298C genotypes stratified by age and gender</p

    Summary of the original international literature investigating the association of the <i>MTHFR</i> C677T genotypes with childhood leukemia.

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    <p>Note: Some studies that had less than 70 cases and 70 controls of a redundant population were not included.</p><p>The survey of literature was updated 2014/09/18.</p><p>Summary of the original international literature investigating the association of the <i>MTHFR</i> C677T genotypes with childhood leukemia.</p

    Additional file 1 of Indigofera suffruticosa aerial parts extract induce G2/M arrest and ATR/CHK1 pathway in Jurkat cells

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    Additional file 1: Supplementary Table S1. Antibodies used in this study. Supplementary Fig. S1. Representative plot of Annexin V staining results. This figure is related to Fig. 2D. Supplementary Fig. S2. The caspase-3/7 activities in Jurkat cells after 12 h of ISAE treatment were assessed by Caspase-Glo® 3/7 assay (Promega) according to the manufacturer's instructions. The graph was expressed as fold changes to control group. Supplementary Fig. S3. Relative quantitative analysis of tryptanthrin, indigo, and indirubin in ISAE. The selected ion current chromatograms of the ISAE extract, tryptanthrin, indigo, and indirubin were carried out through MS full scan experiment in positive mode. The relative abundance of the three selected compounds in ISAE extract were calculated based on comparing the peak area ratios with standard compounds. Supplementary Fig. S4. Cell gating for cell cycle analysis. For cell cycle analysis, cells were gated using forward scatter (FSC) and side scatter (SSC) properties. This helped in excluding cell debris and selecting the desired cells (within the black circle) for analysis. The gating area was established based on the solvent control group (0 μg/mL of ISAE) and was consistently applied to all other groups. This illustration corresponds to Fig. 2A. Original images of western blot. Multiple exposure images of WB
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