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Yingchun Hou

Researcher at Shaanxi Normal University

Publications -  37
Citations -  748

Yingchun Hou is an academic researcher from Shaanxi Normal University. The author has contributed to research in topics: Cancer & Peptide library. The author has an hindex of 10, co-authored 31 publications receiving 468 citations.

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Aptamer-mediated survivin RNAi enables 5-fluorouracil to eliminate colorectal cancer stem cells

TL;DR: The results indicate that survivin is one of the key players responsible for the innate chemoresistance of colorectal cancer stem cells and aptamer-mediated targeting of survivin in cancerstem cells in combination with chemotherapeutic drugs constitutes a new avenue to improve treatment outcome in oncologic clinics.
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Effects of miR-29a and miR-101a expression on myocardial interstitial collagen generation after aerobic exercise in myocardial-infarcted rats

TL;DR: It is believed that controlled intermittent aerobic exercise is beneficial to the healing and discovery of damaged cardiac tissues and their function after MI and inhibit TGFβ pathway via up-regulation to the expression of microRNAs and miR-101a and finally cause a reduced fibrosis and scar formation in cardiac tissue.
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The inhibition of ABCB1/MDR1 or ABCG2/BCRP enables doxorubicin to eliminate liver cancer stem cells

TL;DR: In this article, the authors explored the role of inhibition of MDR1 or ABCG2 in sensitizing liver cancer stem cells to doxorubicin, the most frequently used chemotherapeutic agent in treating liver cancer.
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A Detailed Protein-SELEX Protocol Allowing Visual Assessments of Individual Steps for a High Success Rate

TL;DR: An improved protein-SELEX procedure is presented for simplified and highly efficient isolation of aptamers against protein targets, and a simplified sample preparation method for MiSeq-based next-generation sequencing is introduced.
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ANXA2 enhances the progression of hepatocellular carcinoma via remodeling the cell motility associated structures

TL;DR: The results indicate that ANXA2 plays an important role to enhance the malignant behaviors of HCC cells, and the enhancement is closely based on its remodeling to cell structures.