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Robert E Scott

Showing results (1-10 of 9) with videos related to

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Journal of Cellular Physiology|October 18, 2002
P2P-R protein overexpression restricts mitotic progression at prometaphase and promotes mitotic apoptosisSizhi Gao, Robert E Scott
Journal of Cellular Physiology|June 18, 2002
P2P-R protein localizes to the nucleolus of interphase cells and the periphery of chromosomes in mitotic cells which show maximum P2P-R immunoreactivitySizhi Gao, Michael M Witte, Robert E Scott
Current Sports Medicine Reports|July 2, 2003
Traumatic hip dislocation in athletesChris S Pallia, Robert E Scott, David J Chao
Journal of Cellular Biochemistry|August 26, 2003
Functional potential of P2P-R: a role in the cell cycle and cell differentiation related to its interactions with proteins that bind to matrix associated regions of DNA?Robert E Scott, Thomas Giannakouros, Sizhi Gao, et al.
Differentiation; Research in Biological Diversity|September 6, 2005
De-differentiation-derived mesenchymal stem cells demonstrate selective repression in H19 bioregulatory RNA gene expressionRobert E Scott, Sizhi Gao, Chung-Kwan Kim, et al.
Journal of Cellular Physiology|March 27, 2015
Cell cycle gene expression networks discovered using systems biology: Significance in carcinogenesisRobert E Scott, Prachi N Ghule, Janet L Stein, et al.
BMC Systems Biology|February 27, 2010
Systems genetics analyses predict a transcription role for P2P-R: molecular confirmation that P2P-R is a transcriptional co-repressorPhilippos Peidis, Thomas Giannakouros, Matthew E Burow, et al.
Journal of Cellular Physiology|December 24, 2004
P2P-R expression is genetically coregulated with components of the translation machinery and with PUM2, a translational repressor that associates with the P2P-R mRNARobert E Scott, Erica White-Grindley, H Earl Ruley, et al.
FEBS Letters|December 7, 2010
SAFB1 interacts with and suppresses the transcriptional activity of p53Philippos Peidis, Nikolaos Voukkalis, Eleni Aggelidou, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Journal of Cellular Physiology|October 18, 2002
P2P-R protein overexpression restricts mitotic progression at prometaphase and promotes mitotic apoptosisSizhi Gao, Robert E Scott
Journal of Cellular Physiology|June 18, 2002
P2P-R protein localizes to the nucleolus of interphase cells and the periphery of chromosomes in mitotic cells which show maximum P2P-R immunoreactivitySizhi Gao, Michael M Witte, Robert E Scott
Current Sports Medicine Reports|July 2, 2003
Traumatic hip dislocation in athletesChris S Pallia, Robert E Scott, David J Chao
Journal of Cellular Biochemistry|August 26, 2003
Functional potential of P2P-R: a role in the cell cycle and cell differentiation related to its interactions with proteins that bind to matrix associated regions of DNA?Robert E Scott, Thomas Giannakouros, Sizhi Gao, et al.
Differentiation; Research in Biological Diversity|September 6, 2005
De-differentiation-derived mesenchymal stem cells demonstrate selective repression in H19 bioregulatory RNA gene expressionRobert E Scott, Sizhi Gao, Chung-Kwan Kim, et al.
Journal of Cellular Physiology|March 27, 2015
Cell cycle gene expression networks discovered using systems biology: Significance in carcinogenesisRobert E Scott, Prachi N Ghule, Janet L Stein, et al.
BMC Systems Biology|February 27, 2010
Systems genetics analyses predict a transcription role for P2P-R: molecular confirmation that P2P-R is a transcriptional co-repressorPhilippos Peidis, Thomas Giannakouros, Matthew E Burow, et al.
Journal of Cellular Physiology|December 24, 2004
P2P-R expression is genetically coregulated with components of the translation machinery and with PUM2, a translational repressor that associates with the P2P-R mRNARobert E Scott, Erica White-Grindley, H Earl Ruley, et al.
FEBS Letters|December 7, 2010
SAFB1 interacts with and suppresses the transcriptional activity of p53Philippos Peidis, Nikolaos Voukkalis, Eleni Aggelidou, et al.
Pageof 1