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rdf:type |
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lifeskim:mentions |
umls-concept:C0007586,
umls-concept:C0007634,
umls-concept:C0017262,
umls-concept:C0020792,
umls-concept:C0025663,
umls-concept:C0035696,
umls-concept:C0079395,
umls-concept:C0205087,
umls-concept:C0887824,
umls-concept:C1171362,
umls-concept:C1512505,
umls-concept:C1515670
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pubmed:issue |
4
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pubmed:dateCreated |
1997-1-2
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pubmed:databankReference |
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pubmed:abstractText |
The decision for a cell to enter the DNA synthesis (S) phase of the cell cycle or to arrest in quiescence is likely to be determined by genes expressed in the late G1 phase, at the restriction point. Loss of restriction point control is associated with malignant cellular transformation and cancer. For this reason, identifying genes that are differentially expressed in late G1 phase versus quiescence is important for understanding the molecular basis of normal and malignant growth.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-1354393,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-1406627,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-1458489,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-1538751,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-1977518,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-2259383,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-2683075,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-4128323,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-4524638,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-6355085,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-7622060,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-7673167,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-7721891,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-7760935,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-7809069,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-7838734,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-7929410,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-8175725,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-8187880,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8827717-8341601
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1076-1551
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
2
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
469-78
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:8827717-Base Sequence,
pubmed-meshheading:8827717-Blotting, Northern,
pubmed-meshheading:8827717-Breast Neoplasms,
pubmed-meshheading:8827717-DNA, Complementary,
pubmed-meshheading:8827717-Female,
pubmed-meshheading:8827717-G0 Phase,
pubmed-meshheading:8827717-G1 Phase,
pubmed-meshheading:8827717-Humans,
pubmed-meshheading:8827717-Molecular Sequence Data,
pubmed-meshheading:8827717-RNA, Messenger,
pubmed-meshheading:8827717-Tumor Cells, Cultured
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pubmed:year |
1996
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pubmed:articleTitle |
Identification of mRNAs differentially expressed in quiescence or in late G1 phase of the cell cycle in human breast cancer cells by using the differential display method.
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pubmed:affiliation |
Division of Cell Growth and Regulation, Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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