scholarly journals Temporal differences in DNA replication during the S phase using single fiber analysis of normal human fibroblasts and glioblastoma T98G cells

Cell Cycle ◽  
2009 ◽  
Vol 8 (19) ◽  
pp. 3133-3148 ◽  
Author(s):  
Rebecca A. Frum ◽  
Zakaria S. Khondker ◽  
David G. Kaufman
Cell Cycle ◽  
2013 ◽  
Vol 12 (2) ◽  
pp. 332-345 ◽  
Author(s):  
Stephanie L. Smith-Roe ◽  
Shivani S. Patel ◽  
Yingchun Zhou ◽  
Dennis A. Simpson ◽  
Shangbang Rao ◽  
...  

1998 ◽  
Vol 245 (2) ◽  
pp. 321-329 ◽  
Author(s):  
Stephanie M. Cohen ◽  
Erica R. Cobb ◽  
Marila Cordeiro-Stone ◽  
David G. Kaufman

2000 ◽  
Vol 99 (2) ◽  
pp. 186-190 ◽  
Author(s):  
Yasutoshi Koga ◽  
Atsuko Koga ◽  
Rikako Iwanaga ◽  
Yukihiro Akita ◽  
Junko Tubone ◽  
...  

Author(s):  
Bruna P. Brylawski ◽  
Stephanie M. Cohen ◽  
Jonathan L. Longmire ◽  
Norman A. Doggett ◽  
Marila Cordeiro-Stone ◽  
...  

2001 ◽  
Vol 46 (6) ◽  
pp. 15151J ◽  
Author(s):  
Liling Cho ◽  
John A. Reffner ◽  
Barbara M. Gatewood ◽  
David L. Wetzel

1990 ◽  
Vol 97 (3) ◽  
pp. 473-478
Author(s):  
I.R. Kill ◽  
S. Shall

The characteristic limited reproductive life-span of normal human fibroblasts in culture is due to a steadily decreasing fraction of cells able to proliferate in the standard rich growth media. We have observed that restricting the growth factor supply to old cells for variable lengths of time in culture increases the fraction of cells that can enter S-phase; although these cells do not go on to divide. Thus, it seems that there is a transient phase between the proliferating state and the irreversibly post-mitotic, senescent state. Perhaps a ‘quiescent-G0’ state, which can be maintained in the presence of growth factors, is a stage on the pathway to mortalization and senescence.


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