CG&D
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cell Growth & Differentiation

Right arrow Help viewing high resolution images
Right arrow Return to article
Click on image to view larger version.



Fig. 5. Constitutively active ErbB4 mutants do not increase the growth rate of FR3T3 fibroblasts. FR3T3 cells that express the LXSN vector control, the constitutively active ErbB2* mutant, wild-type ErbB4, or the constitutively active ErbB4 mutants (Q646C, H647C, and A648C) were plated at a density of 2 x 104 cells in 60-mm dishes (700 cells/cm2) and were incubated for 1–10 days. Cells were counted daily to assess growth rates and saturation densities. The means for three independent experiments; bars, SE.





Right arrow Return to article


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cell Growth & Differentiation