Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Published Erratum
. 2025 Aug 26;122(34):e2519923122.
doi: 10.1073/pnas.2519923122. Epub 2025 Aug 20.

Correction for Kuroda et al., Bim and Bad mediate imatinib-induced killing of Bcr/Abl+ leukemic cells, and resistance due to their loss is overcome by a BH3 mimetic

No authors listed
Published Erratum

Correction for Kuroda et al., Bim and Bad mediate imatinib-induced killing of Bcr/Abl+ leukemic cells, and resistance due to their loss is overcome by a BH3 mimetic

No authors listed. Proc Natl Acad Sci U S A. .
No abstract available

PubMed Disclaimer

Figures

Fig. 1.
Fig. 1.
Treatment with imatinib induces increased Bim expression and Bim dephosphorylation in Ph1+ human leukemic cells. K562 cells (A) or BV173 cells (B) were treated for the indicated amount of time with the indicated doses of imatinib. Western blotting was performed with an anti-Bim antibody and as a loading control with antibodies to HSP70 or β-actin. (C) K562 cells were treated for 3 or 6 h with 1 μM imatinib. Semiquantitative RT-PCR was performed to determine levels of bim mRNA (cycles: 25, 30, and 35). Semiquantitative RT-PCR for β-actin mRNA was used as a control (cycles: 20, 25, and 30). (D) K562 cells were left untreated or were treated for 24 h with 1.5 μM imatinib. Bim proteins were purified on an anti-Bim antibody affinity column and then analyzed by 2D gel electrophoresis. Arrows indicate the position of highly phosphorylated Bim from untreated cells.

Erratum for

Publication types

LinkOut - more resources