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Publication : Endogenous E2F-1 promotes timely G0 exit of resting mouse embryo fibroblasts.

First Author  Wang ZM Year  1998
Journal  Proc Natl Acad Sci U S A Volume  95
Issue  26 Pages  15583-6
PubMed ID  9861012 Mgi Jnum  J:119885
Mgi Id  MGI:3703414 Doi  10.1073/pnas.95.26.15583
Citation  Wang ZM, et al. (1998) Endogenous E2F-1 promotes timely G0 exit of resting mouse embryo fibroblasts. Proc Natl Acad Sci U S A 95(26):15583-6
abstractText  Much evidence strongly suggests a positive role for one or more E2F species in the control of exit from G0/G1. Results described here provide direct evidence that endogenous E2F-1, as predicted, contributes to progression from G0 to S. By contrast, cycling cells lacking an intact E2F-1 gene demonstrated normal cell cycle distribution. Therefore, E2F-1 exerts a unique function leading to timely G0 exit of resting cultured primary cells, while at the same time being unnecessary for normal G1 to S phase progression of cycling cells.
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