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[PDF][PDF] Structure, recognition, and processing of cisplatin− DNA adducts
ER Jamieson, SJ Lippard - Chemical reviews, 1999 - Citeseer
In the course of examining the effect of electric fields on the growth of Escherichia coli cells,
a biological activity of platinum compounds was uncovered that led to the development of …
a biological activity of platinum compounds was uncovered that led to the development of …
[PDF][PDF] p53: puzzle and paradigm.
LJ Ko, C Prives - Genes & development, 1996 - researchgate.net
As the tale of p53 unfolds, it becomes ever more intriguing. Although our understanding of
the critical and complex roles played by p53 is progressing rapidly, new findings continue to …
the critical and complex roles played by p53 is progressing rapidly, new findings continue to …
The Tumor Suppressor p53 Down-Regulates Glucose Transporters GLUT1 and GLUT4 Gene Expression
F Schwartzenberg-Bar-Yoseph, M Armoni… - Cancer …, 2004 - aacrjournals.org
Tumorigenesis is associated with enhanced cellular glucose uptake and increased
metabolism. Because the p53 tumor suppressor is mutated in a large number of cancers, we …
metabolism. Because the p53 tumor suppressor is mutated in a large number of cancers, we …
Mitochondrial p53 activates Bak and causes disruption of a Bak–Mcl1 complex
JIJ Leu, P Dumont, M Hafey, ME Murphy… - Nature cell …, 2004 - nature.com
The tumour suppressor activity of the p53 protein has been explained by its ability to induce
apoptosis in response to a variety of cellular stresses,. Thus, understanding the mechanism …
apoptosis in response to a variety of cellular stresses,. Thus, understanding the mechanism …
Twenty years of p53 research: structural and functional aspects of the p53 protein
P May, E May - Oncogene, 1999 - nature.com
From its modest beginnings in 1979, as a transformation-associated protein, to the
discoveries that p53 plays a key role in tumour suppression and in the cellular response to …
discoveries that p53 plays a key role in tumour suppression and in the cellular response to …
p53 levels, functional domains, and DNA damage determine the extent of the apoptotic response of tumor cells.
X Chen, LJ Ko, L Jayaraman, C Prives - Genes & development, 1996 - genesdev.cshlp.org
It is well established that induction of the p53 tumor suppressor protein in cells can lead to
either cell cycle arrest or apoptosis. To further understand features of p53 that contribute to …
either cell cycle arrest or apoptosis. To further understand features of p53 that contribute to …
Mutant p53 exerts a dominant negative effect by preventing wild-type p53 from binding to the promoter of its target genes
A Willis, EJ Jung, T Wakefield, X Chen - Oncogene, 2004 - nature.com
Mutation of the p53 tumor suppressor gene is the most common genetic alteration in human
cancer. A majority of these mutations are missense mutations in the DNA-binding domain …
cancer. A majority of these mutations are missense mutations in the DNA-binding domain …
The transactivation domains of the p53 protein
N Raj, LD Attardi - Cold Spring Harbor …, 2017 - perspectivesinmedicine.cshlp.org
The p53 tumor suppressor is a transcriptional activator, with discrete domains that
participate in sequence-specific DNA binding, tetramerization, and transcriptional activation …
participate in sequence-specific DNA binding, tetramerization, and transcriptional activation …
Nitric oxide-induced p53 accumulation and regulation of inducible nitric oxide synthase expression by wild-type p53.
K Forrester, S Ambs, SE Lupold, RB Kapust… - Proceedings of the …, 1996 - pnas.org
The tumor suppressor gene product p53 plays an important role in the cellular response to
DNA damage from exogenous chemical and physical mutagens. Therefore, we …
DNA damage from exogenous chemical and physical mutagens. Therefore, we …
Molecular epidemiology of human cancer: contribution of mutation spectra studies of tumor suppressor genes
SP Hussain, CC Harris - Cancer Res, 1998 - aacrjournals.org
Volume 58 Issue 18 | Cancer Research | American Association for Cancer Research Skip to
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