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The Effect of miR-338-3p on HBx Deletion-Mutant (HBx-d382) Mediated Liver-Cell Proliferation through CyclinD1 Regulation

Overview of attention for article published in PLOS ONE, August 2012
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Title
The Effect of miR-338-3p on HBx Deletion-Mutant (HBx-d382) Mediated Liver-Cell Proliferation through CyclinD1 Regulation
Published in
PLOS ONE, August 2012
DOI 10.1371/journal.pone.0043204
Pubmed ID
Authors

Xiaoyu Fu, Deming Tan, Zhouhua Hou, Zhiliang Hu, Guozhen Liu, Yi Ouyang, Fei Liu

Abstract

Hepatitis B Virus (HBV) DNA integration and HBV X (HBx) deletion mutation occurs in HBV-positive liver cancer patients, and C-terminal deletion in HBx gene mutants are highly associated with hepatocarcinogenesis. Our previous study found that the HBx-d382 deletion mutant (deleted at nt 382-400) can down-regulate miR-338-3p expression in HBx-expressing cells. The aim of the present study is to examine the role of miR-338-3p in the HBx-d382-mediated liver-cell proliferation.

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The data shown below were compiled from readership statistics for 17 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
China 1 6%
Unknown 16 94%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 29%
Student > Bachelor 3 18%
Other 2 12%
Student > Ph. D. Student 2 12%
Student > Postgraduate 2 12%
Other 3 18%
Readers by discipline Count As %
Agricultural and Biological Sciences 7 41%
Medicine and Dentistry 4 24%
Biochemistry, Genetics and Molecular Biology 2 12%
Veterinary Science and Veterinary Medicine 1 6%
Nursing and Health Professions 1 6%
Other 1 6%
Unknown 1 6%