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P19(ARF) stabilizes p53 by blocking nucleo-cytoplasmic shuttling of Mdm2
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title
P19(ARF) stabilizes p53 by blocking nucleo-cytoplasmic shuttling of Mdm2
(English)
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author name string
W Tao
series ordinal
1
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A J Levine
series ordinal
2
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language of work or name
English
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publication date
8 June 1999
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published in
Proceedings of the National Academy of Sciences of the United States of America
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volume
96
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page(s)
6937-41
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issue
12
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cites work
Nucleocytoplasmic shuttling of oncoprotein Hdm2 is required for Hdm2-mediated degradation of p53
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PubMed Central
reference URL
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retrieved
7 April 2017
ARF promotes MDM2 degradation and stabilizes p53: ARF-INK4a locus deletion impairs both the Rb and p53 tumor suppression pathways
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PubMed Central
reference URL
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7 April 2017
Mdm2 promotes the rapid degradation of p53
1 reference
stated in
PubMed Central
reference URL
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7 April 2017
Amphibian transcription factor IIIA proteins contain a sequence element functionally equivalent to the nuclear export signal of human immunodeficiency virus type 1 Rev
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PubMed Central
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7 April 2017
The ribosomal L5 protein is associated with mdm-2 and mdm-2-p53 complexes
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PubMed Central
reference URL
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7 April 2017
UV Irradiation Stimulates Levels of p53 Cellular Tumor Antigen in Nontransformed Mouse Cells
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PubMed Central
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7 April 2017
Regulation of p53 stability by Mdm2
1 reference
stated in
PubMed Central
reference URL
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7 April 2017
p53, the cellular gatekeeper for growth and division
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PubMed Central
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The retinoblastoma protein and cell cycle control
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7 April 2017
The Ink4a tumor suppressor gene product, p19Arf, interacts with MDM2 and neutralizes MDM2's inhibition of p53
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PubMed Central
reference URL
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7 April 2017
Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest
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PubMed Central
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7 April 2017
The mdm-2 oncogene product forms a complex with the p53 protein and inhibits p53-mediated transactivation
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PubMed Central
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The E6 oncoprotein encoded by human papillomavirus types 16 and 18 promotes the degradation of p53
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p53: puzzle and paradigm
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7 April 2017
Oncoprotein MDM2 conceals the activation domain of tumour suppressor p53
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PubMed Central
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7 April 2017
mdm2 expression is induced by wild type p53 activity
1 reference
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PubMed Central
reference URL
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7 April 2017
Nuclear export is required for degradation of endogenous p53 by MDM2 and human papillomavirus E6
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PubMed Central
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Functional and physical interactions of the ARF tumor suppressor with p53 and Mdm2
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PubMed Central
reference URL
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Nucleo-cytoplasmic shuttling of the hdm2 oncoprotein regulates the levels of the p53 protein via a pathway used by the human immunodeficiency virus rev protein.
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PubMed Central
reference URL
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Effects of anti-fibrillarin antibodies on building of functional nucleoli at the end of mitosis.
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28 September 2017
The MDM2 oncoprotein binds specifically to RNA through its RING finger domain
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stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22020
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28 September 2017
Mouse-human heterokaryon analysis with a 33258 Hoechst-Giemsa technique
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PubMed Central
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28 September 2017
Tumor surveillance via the ARF-p53 pathway.
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PubMed Central
reference URL
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28 November 2018
The nucleolus.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22020
retrieved
28 November 2018
Protein-mediated nuclear export of RNA: 5S rRNA containing small RNPs in xenopus oocytes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10359817
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1073/PNAS.96.12.6937
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2140469
ADS bibcode
1999PNAS...96.6937T
0 references
OpenCitations bibliographic resource ID
2140469
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2140469
PMCID
22020
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2140469
PubMed ID
10359817
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2140469
ResearchGate publication ID
12938780
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