Nuclear localization of the transcriptional regulator MIER1α requires interaction with HDAC1/2 in breast cancer cells (Q35078325)

6 August 2017

title

Nuclear localization of the transcriptional regulator MIER1α requires interaction with HDAC1/2 in breast cancer cells (English)

1 reference

6 August 2017

Shengnan Li

1

1 reference

6 August 2017

Gary D Paterno

series ordinal

2

1 reference

6 August 2017

Laura L Gillespie

series ordinal

3

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6 August 2017

language of work or name

English

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publication date

20 December 2013

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6 August 2017

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6 August 2017

volume

8

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6 August 2017

issue

12

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6 August 2017

page(s)

e84046

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Creative Commons Attribution 4.0 International

6 August 2017

copyright license

start time

20 December 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3869823/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

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Differential splicing alters subcellular localization of the alpha but not beta isoform of the MIER1 transcriptional regulator in breast cancer cells

8 July 2018

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8 July 2018

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Changes in subcellular localisation of MI-ER1 alpha, a novel oestrogen receptor-alpha interacting protein, is associated with breast cancer progression

8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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27 September 2018

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A SOX9 defect of calmodulin-dependent nuclear import in campomelic dysplasia/autosomal sex reversal

27 September 2018

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27 September 2018

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Identification of phosphorylated proteins associated with the fibroblast growth factor receptor type I during early Xenopus development.

27 September 2018

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cDNA cloning of a novel, developmentally regulated immediate early gene activated by fibroblast growth factor and encoding a nuclear protein

27 September 2018

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10.1371/JOURNAL.PONE.0084046

27 September 2018

Identifiers

DOI

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6 August 2017

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1 reference

6 August 2017

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