Rescue of early embryonic lethality in mdm2-deficient mice by deletion of p53 (Q29617850)

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scientific article (publication date: 9 November 1995)

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English	Rescue of early embryonic lethality in mdm2-deficient mice by deletion of p53	scientific article (publication date: 9 November 1995)

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title

Rescue of early embryonic lethality in mdm2-deficient mice by deletion of p53 (English)

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PubMed

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author

Roberto Montes-de-Oca-Luna

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Montes de Oca Luna R

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author name string

Wagner DS

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2

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Lozano G

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3

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PubMed

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language of work or name

English

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publication date

9 November 1995

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published in

Nature

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volume

378

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issue

6553

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page(s)

203-6

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cites work

Presence of a potent transcription activating sequence in the p53 protein

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Crossref

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https://api.crossref.org/works/10.1038%2F378203A0

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7 January 2021

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Transcriptional activation by wild-type but not transforming mutants of the p53 anti-oncogene

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https://api.crossref.org/works/10.1038%2F378203A0

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WAF1, a potential mediator of p53 tumor suppression

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Crossref

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https://api.crossref.org/works/10.1038%2F378203A0

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7 January 2021

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The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases

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https://api.crossref.org/works/10.1038%2F378203A0

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A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia-telangiectasia

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https://api.crossref.org/works/10.1038%2F378203A0

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p53 is required for radiation-induced apoptosis in mouse thymocytes

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Thymocyte apoptosis induced by p53-dependent and independent pathways.

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7 January 2021

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A novel form of Epstein-Barr virus latency in normal B cells in vivo

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7 January 2021

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Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours

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Crossref

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7 January 2021

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Tumor spectrum analysis in p53-mutant mice

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https://api.crossref.org/works/10.1038%2F378203A0

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7 January 2021

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The mdm-2 oncogene product forms a complex with the p53 protein and inhibits p53-mediated transactivation

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Crossref

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https://api.crossref.org/works/10.1038%2F378203A0

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7 January 2021

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Mapping of the p53 and mdm-2 Interaction Domains

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Crossref

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https://api.crossref.org/works/10.1038%2F378203A0

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7 January 2021

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Oncoprotein MDM2 conceals the activation domain of tumour suppressor p53

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https://api.crossref.org/works/10.1038%2F378203A0

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7 January 2021

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Amplification of a gene encoding a p53-associated protein in human sarcomas

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7 January 2021

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The mdm-2 oncogene can overcome wild-type p53 suppression of transformed cell growth

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Crossref

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https://api.crossref.org/works/10.1038%2F378203A0

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7 January 2021

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UV Irradiation Stimulates Levels of p53 Cellular Tumor Antigen in Nontransformed Mouse Cells

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Crossref

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https://api.crossref.org/works/10.1038%2F378203A0

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7 January 2021

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Wild-type p53 is a cell cycle checkpoint determinant following irradiation

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Crossref

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https://api.crossref.org/works/10.1038%2F378203A0

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7 January 2021

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Differential induction of transcriptionally active p53 following UV or ionizing radiation: defects in chromosome instability syndromes?

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7 January 2021

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p53-dependent apoptosis modulates the cytotoxicity of anticancer agents

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7 January 2021

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DNA damage triggers a prolonged p53-dependent G1 arrest and long-term induction of Cip1 in normal human fibroblasts

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Interaction between the retinoblastoma protein and the oncoprotein MDM2

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7 January 2021

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Stimulation of E2F1/DP1 transcriptional activity by MDM2 oncoprotein

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7 January 2021

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Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice

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Disruption of the proto-oncogene int-2 in mouse embryo-derived stem cells: a general strategy for targeting mutations to non-selectable genes

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The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain

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Crossref

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7 January 2021

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Identifiers

DOI

10.1038/378203A0

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PubMed

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7477326

retrieved

30 April 2017

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

894684

Dimensions Publication ID

1015059358

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OpenCitations bibliographic resource ID

894684

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

894684

PubMed publication ID

7477326

2 references

stated in

PubMed

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7477326

retrieved

30 April 2017

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

894684

 

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