Clinical and molecular relevance of genetic variants in the non-coding transcriptome of patients with cytogenetically normal acute myeloid leukemia.

Haematologica · 2022 · PMC9052895 · PMID 34261293

Europe PMC DOI

hedged sentences

0.0900

closest p · 1.8× alpha

0.0900

boldest claim

The sentences

showed a trendP =0.09so close (0.05 < p ≤ 0.1)

21%) and showed a trend for longer OS ( P =0.09; 5-year rates: 43% vs . 34%; Figures 2 A to C; Online Supplementary Table S4 ).

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did not reach statistical significanceno p-value reported

Regarding cell viability, ectopic overexpression of the SNHG15 wt and the SNHG15 varT led to a discreet but consistent decrease in cell viability across cell lines, which did not reach statistical significance ( Figures 4C and D ).

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