Exact(56)
The study enrolled 304 patients with Ph− ALL (Table 1).
The results were similar when we analysed only children with ALL (Table 3).
We collected peripheral blood at diagnosis and remission bone marrow from four patients with congenital ALL (Table 1).
We used xenografted cells from n = 11 children with different subtypes and risk status of ALL (Table 1).
There were three PTC‐resistant (ED50 > 10 μM) cell lines, and they were all derived from ALL (Table 1).
Among patients for whom information was available, 33.3% (8/24) had an underlying disease, including 2 children with acute lymphoblastic leukemia (ALL) (Table A1).
For this comparative evaluation we used our human union dataset ALL (Table 2), in which PPIs have at least one line of supporting evidence.
Significant associations were not observed for rhinitis and other allergies in children with AL and ALL (Table 3 and Supplementary Table).
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Similar(2)
We further classified the study subjects into T-ALL and B-ALL (Table 3).
We did not observe a significant difference in the frequency of WT1 mutations between ETP-ALL and the remaining T-ALL (Table 2).
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