Although high SFXN3 expression was also associated with reduced survival in patients aged ≤ 60 years, the difference did not reach statistical significance (HR = 1.56, 95 % CI: 0.81–3.00, P = 0.180), suggesting a stronger prognostic implication of SFXN3 in elderly individuals.
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REST-driven upregulation of SFXN3 promotes AML progression via Wnt/β-catenin activation and confers decitabine resistance.
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0.1800