MDM4 regulation by the let-7 miRNA family in the DNA damage response of glioma cells (Q38869089)

7 September 2017

MDM4 regulation by the let-7 miRNA family in the DNA damage response of glioma cells (English)

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7 September 2017

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Chen Xie

1

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7 September 2017

Wei Chen

2

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7 September 2017

Mengdie Zhang

3

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7 September 2017

Qiuxian Cai

4

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7 September 2017

Weiyi Xu

5

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7 September 2017

Xiaodi Li

6

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7 September 2017

Songshan Jiang

7

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7 September 2017

language of work or name

English

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publication date

27 May 2015

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7 September 2017

8

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based on heuristic

inferred from page(s)

published in

FEBS Letters

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7 September 2017

589

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7 September 2017

15

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7 September 2017

1958-1965

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MicroRNAs to Nanog, Oct4 and Sox2 coding regions modulate embryonic stem cell differentiation

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Amplification of Mdmx (or Mdm4) directly contributes to tumor formation by inhibiting p53 tumor suppressor activity

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ATM and Chk2-dependent phosphorylation of MDMX contribute to p53 activation after DNA damage

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An illegitimate microRNA target site within the 3' UTR of MDM4 affects ovarian cancer progression and chemosensitivity

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Let-7 microRNA inhibits the proliferation of human glioblastoma cells

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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

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Comprehensive genomic characterization defines human glioblastoma genes and core pathways

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LIN28B confers radio-resistance through the posttranscriptional control of KRAS.

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The RNA-binding protein KSRP promotes the biogenesis of a subset of microRNAs

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A mammalian microRNA expression atlas based on small RNA library sequencing

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A let-7 microRNA-binding site polymorphism in 3'-untranslated region of KRAS gene predicts response in wild-type KRAS patients with metastatic colorectal cancer treated with cetuximab monotherapy

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21 January 2018

Identifiers

DOI

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7 September 2017

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