Functionally distinct polymorphic sequences in the human genome that are targets for p53 transactivation. (Q33772124)

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11 January 2020

title

Functionally distinct polymorphic sequences in the human genome that are targets for p53 transactivation (English)

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11 January 2020

8

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11 January 2020

Douglas A Bell

7

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author name string

Daniel J Tomso

1

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11 January 2020

Alberto Inga

2

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11 January 2020

Daniel Menendez

3

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11 January 2020

Gary S Pittman

4

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11 January 2020

Michelle R Campbell

5

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11 January 2020

Francesca Storici

6

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11 January 2020

language of work or name

English

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publication date

20 April 2005

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Proceedings of the National Academy of Sciences of the United States of America

11 January 2020

published in

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volume

102

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issue

18

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page(s)

6431-6436

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describes a project that uses

11 January 2020

SQL

1 reference

26 June 2022

https://europepmc.org/article/PMC/PMC1088378

inferred from PubMed Central ID database lookup

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A novel polymorphic CAAT/enhancer-binding protein beta element in the FasL gene promoter alters Fas ligand expression: a candidate background gene in African American systemic lupus erythematosus patients

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Differential transactivation by the p53 transcription factor is highly dependent on p53 level and promoter target sequence.

4 July 2018

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The dependence receptor DCC (deleted in colorectal cancer) defines an alternative mechanism for caspase activation

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12 December 2020

Groups of p53 target genes involved in specific p53 downstream effects cluster into different classes of DNA binding sites

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12 December 2020

Wanted: regulatory SNPs

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Identifiers

DOI

10.1073/PNAS.0501721102

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15843459 AND SRC:MED&resulttype=core&format=json

11 January 2020

0 references

1 reference

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11 January 2020

PubMed publication ID

15843459

1 reference