miR-376a suppresses proliferation and induces apoptosis in hepatocellular carcinoma (Q39334033)

11 September 2017

title

miR-376a suppresses proliferation and induces apoptosis in hepatocellular carcinoma (English)

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11 September 2017

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Yongxia Zheng

1

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11 September 2017

Lei Yin

2

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11 September 2017

Huan Chen

3

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11 September 2017

Shengsheng Yang

4

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11 September 2017

Chuanyong Pan

5

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11 September 2017

Shan Lu

6

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11 September 2017

Mingyong Miao

7

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11 September 2017

Binghua Jiao

8

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11 September 2017

language of work or name

English

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publication date

7 June 2012

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11 September 2017

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11 September 2017

volume

586

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11 September 2017

issue

16

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11 September 2017

page(s)

2396-2403

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MicroRNAs: genomics, biogenesis, mechanism, and function

11 September 2017

cites work

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DLK1-DIO3 Genomic Imprinted MicroRNA Cluster at 14q32.2 Defines a Stemlike Subtype of Hepatocellular Carcinoma Associated with Poor Survival

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Liver regeneration associated protein (ALR) exhibits antimetastatic potential in hepatocellular carcinoma.

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Genomewide microRNA down-regulation as a negative feedback mechanism in the early phases of liver regeneration

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Genomic and epigenetic alterations deregulate microRNA expression in human epithelial ovarian cancer

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Regulation of erythroid differentiation by miR-376a and its targets

21 January 2018

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Relationship between serum alpha-foetoprotein, cirrhosis and survival in hepatocellular carcinoma

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High alpha-fetoprotein level correlates with high stage, early recurrence and poor prognosis of hepatocellular carcinoma: significance of hepatitis virus infection, age, p53 and beta-catenin mutations.

21 January 2018

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Desperately seeking microRNA targets

21 January 2018

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Impaired B cell development and proliferation in absence of phosphoinositide 3-kinase p85alpha.

21 January 2018

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Suppression of the PI3K subunit p85α delays embryoid body development and inhibits cell adhesion.

21 January 2018

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miR-29 miRNAs activate p53 by targeting p85 alpha and CDC42.

21 January 2018

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10.1016/J.FEBSLET.2012.05.054

21 January 2018

Identifiers

DOI

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11 September 2017

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