Additional supporting information may be found online in the Supporting Information section at the end of the article. Fig S1. (A, B, C) Relapse stage flow results showed the blast cells were positive for HLA-DR, CD13, CD33, CD117 and CD34. (D) Empty vector and HA-tagged TFG-FGFR1 were expressed in 293T cells. Immunoblotting analysis of the expression of FGFR1, SHI1, BCL2 and KLF4 were performed in 293T cells. Signal quantification was performed using Ima-geJ software. For each antibody, we did multiple repeat experiments; only representative results are shown. (E) HL60 cell line with TFG-FGFR1 showed reduced cell viability when cultured with imatinib or ponatinib in vitro. The cellular viability was assessed after 48 h in culture with CCK-8. Nonlinear regression curves were fitted for evaluation of IC50 values. Table SI. Next-generation sequencing (a panel of 114 genes). Table SII. Mutations observed in the genes.References . (2013) Inhibition of TFG function causes hereditary axon degeneration by impairing endoplasmic reticulum structure.

Phase measuring is cumbersome and expensive, especially when operation frequency of array is high. To avoid phase measuring, a novel failed sensor localization algorithm using amplitude-only near-field data is proposed. In perspective of Bayesian theory, the maximum a posteriori estimation of array excitation leads to a mixed-norm minimization problem subject to a quadratic constraint. Iterative procedure based on alternating directions method of multipliers is used to solve this problem. Computer simulations show that the proposed algorithm is able to give accurate estimation of array excitation and precisely locate the failed sensors of the array using amplitude-only near-field data.

No abstract

No abstract