Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1987-4-6
pubmed:abstractText
It has been postulated that the expression of the product (p21) encoded by the ras genes may have a role in cell cycle events. Simultaneous multiparameter flow cytometry was used to measure the p21 content in relation to the cell cycle of several cancer cell lines of human origin. These studies revealed that p21 levels rise during the G1 phase of the cycle and remain approximately constant as cells traverse the S and G2 + M phases. The threshold level of p21 expression of S phase cells was used to divide the G1 cell population into cells with low (G1A) and high (G1B) p21 content. The p21 levels of G1B cells were approximately ten times higher than those of G1A cells. The validity of this subdivision was confirmed by synchronous measurements of RNA content and p21. Cells with low RNA content, hence in early part of G1 phase of the cell cycle, expressed low levels of p21, and cells with higher RNA content expressed higher levels of p21. These observations suggest that the levels of p21 are much lower at the onset of the cell cycle than at its end; hence a drop in p21 expression is likely to occur during or immediately after mitotic division.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-2408339, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-2417118, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-2427924, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-2581140, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-3007866, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-3023888, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-3089984, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-3510879, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-3516433, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-3528401, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-3858828, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-3886828, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-3888556, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-3918269, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6101201, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6147754, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6148703, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6170496, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6184378, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6247068, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6283384, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6285471, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6334806, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6351725, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6375822, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6380758, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6397126, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6432310, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6482968, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6493228, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6606489, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6609772, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6611509, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-6692471, http://linkedlifedata.com/resource/pubmed/commentcorrection/3548406-7305346
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0002-9440
pubmed:author
pubmed:issnType
Print
pubmed:volume
126
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
411-6
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1987
pubmed:articleTitle
Expression of Ha-ras oncogene p21 protein in relation to the cell cycle of cultured human tumor cells.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.