Automated Author ProfileYunhai Zhang
Yunhai Zhang
Current S-Index
Sum of Dataset Indices for all datasets
Average Dataset Index per Dataset
Average Dataset Index per dataset
Total Datasets
Total datasets for this author
Average FAIR Score
Average FAIR Score per dataset
Total Citations
Total citations to the author's datasets
Total Mentions
Total mentions of the author's datasets
S-Index Interpretation
The S-Index (Sharing Index) is a comprehensive metric that represents the cumulative impact of all your datasets. It is calculated as the sum of Dataset Index scores across all your claimed datasets.
What it means:
- A higher S-index indicates greater overall impact of your datasets relative to typical datasets in their fields of research
- The S-Index grows as you add more datasets or as existing datasets gain more citations and mentions
- It provides a single number to track your research data impact over time
Current S-Index: 9.6 (sum of 20 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
ABSTRACT This study examined the effects of purmorphamine and cyclopamine, classical agonists and inhibitors of the Hedgehog (Hh) signaling pathway, in the adipogenic differentiation of porcine adipose-derived mesenchymal stem cells (AMSC) to investigate the roles underlying adipogenic differentiation in AMSC. Porcine-derived AMSC were established, and the Hh signaling pathway was activated or inhibited by treatment with purmorphamine or cyclopamine. The adipogenic differentiation of the porcine AMSC was then analyzed by Oil Red O staining. The expression levels of Hh signaling pathway factors and adipogenic transcription factors were determined using quantitative real-time polymerase chain reaction and western blot analysis. We verified that the expression levels of positive regulators of the Hh pathway (Smo, Gli1, Gli2, and Gli3) decreased during adipogenesis, whereas those of negative regulators (Ptc1 and Ptc2) increased. Purmorphamine can inhibit the adipogenic differentiation of porcine AMSC in vitro culture. In addition, both the expression of the CCAAT/enhancerbindingprotein-α and that of the peroxisome proliferator-activated receptor-γ decreased in the presence of purmorphamine. By contrast, cyclopamine had no significant effect on the adipogenic differentiation of porcine AMSC. The Hh signaling pathway inhibits the adipogenic differentiation potential of porcine AMSC.
Authors
- Caiyun Fan ;
- Yunhai Zhang ;
- Juhua Wang ;
- Jianbo Cheng
ABSTRACT This study examined the effects of purmorphamine and cyclopamine, classical agonists and inhibitors of the Hedgehog (Hh) signaling pathway, in the adipogenic differentiation of porcine adipose-derived mesenchymal stem cells (AMSC) to investigate the roles underlying adipogenic differentiation in AMSC. Porcine-derived AMSC were established, and the Hh signaling pathway was activated or inhibited by treatment with purmorphamine or cyclopamine. The adipogenic differentiation of the porcine AMSC was then analyzed by Oil Red O staining. The expression levels of Hh signaling pathway factors and adipogenic transcription factors were determined using quantitative real-time polymerase chain reaction and western blot analysis. We verified that the expression levels of positive regulators of the Hh pathway (Smo, Gli1, Gli2, and Gli3) decreased during adipogenesis, whereas those of negative regulators (Ptc1 and Ptc2) increased. Purmorphamine can inhibit the adipogenic differentiation of porcine AMSC in vitro culture. In addition, both the expression of the CCAAT/enhancerbindingprotein-α and that of the peroxisome proliferator-activated receptor-γ decreased in the presence of purmorphamine. By contrast, cyclopamine had no significant effect on the adipogenic differentiation of porcine AMSC. The Hh signaling pathway inhibits the adipogenic differentiation potential of porcine AMSC.
Authors
- Caiyun Fan ;
- Yunhai Zhang ;
- Juhua Wang ;
- Jianbo Cheng
GO analysis of predicted targets of lncRNAs in cis. (XLS 119Â kb)
Authors
- Xiaoxiao Gao ;
- Ye, Jing ;
- Yang, Chen ;
- Kaifa Zhang ;
- Xiumei Li ;
- Luo, Lei ;
- Jianping Ding ;
- Yunsheng Li ;
- Hongguo Cao ;
- Yinghui Ling ;
- Xiaorong Zhang ;
- Liu, Ya ;
- Fugui Fang ;
- Yunhai Zhang
KEGG pathway analysis of predicted targets of lncRNAs in trans. (XLS 367Â kb)
Authors
- Xiaoxiao Gao ;
- Ye, Jing ;
- Yang, Chen ;
- Kaifa Zhang ;
- Xiumei Li ;
- Luo, Lei ;
- Jianping Ding ;
- Yunsheng Li ;
- Hongguo Cao ;
- Yinghui Ling ;
- Xiaorong Zhang ;
- Liu, Ya ;
- Fugui Fang ;
- Yunhai Zhang
The protein-coding genes as potential targets 10K/100K upstream and downstream of the lncRNAs. (XLSX 372Â kb)
Authors
- Xiaoxiao Gao ;
- Ye, Jing ;
- Yang, Chen ;
- Kaifa Zhang ;
- Xiumei Li ;
- Luo, Lei ;
- Jianping Ding ;
- Yunsheng Li ;
- Hongguo Cao ;
- Yinghui Ling ;
- Xiaorong Zhang ;
- Liu, Ya ;
- Fugui Fang ;
- Yunhai Zhang
The specific expression of lncRNAs in pubertal/prepubertal samples. (XLSX 36Â kb)
Authors
- Xiaoxiao Gao ;
- Ye, Jing ;
- Yang, Chen ;
- Kaifa Zhang ;
- Xiumei Li ;
- Luo, Lei ;
- Jianping Ding ;
- Yunsheng Li ;
- Hongguo Cao ;
- Yinghui Ling ;
- Xiaorong Zhang ;
- Liu, Ya ;
- Fugui Fang ;
- Yunhai Zhang
The expression of protein-coding genes related puberty. (XLSX 10Â kb)
Authors
- Xiaoxiao Gao ;
- Ye, Jing ;
- Yang, Chen ;
- Kaifa Zhang ;
- Xiumei Li ;
- Luo, Lei ;
- Jianping Ding ;
- Yunsheng Li ;
- Hongguo Cao ;
- Yinghui Ling ;
- Xiaorong Zhang ;
- Liu, Ya ;
- Fugui Fang ;
- Yunhai Zhang
The production of reads from the Illumina HiSeq 4000 platform. (XLSX 9Â kb)
Authors
- Xiaoxiao Gao ;
- Ye, Jing ;
- Yang, Chen ;
- Kaifa Zhang ;
- Xiumei Li ;
- Luo, Lei ;
- Jianping Ding ;
- Yunsheng Li ;
- Hongguo Cao ;
- Yinghui Ling ;
- Xiaorong Zhang ;
- Liu, Ya ;
- Fugui Fang ;
- Yunhai Zhang
GO analysis of predicted targets of lncRNAs in trans. (XLS 1551Â kb)
Authors
- Xiaoxiao Gao ;
- Ye, Jing ;
- Yang, Chen ;
- Kaifa Zhang ;
- Xiumei Li ;
- Luo, Lei ;
- Jianping Ding ;
- Yunsheng Li ;
- Hongguo Cao ;
- Yinghui Ling ;
- Xiaorong Zhang ;
- Liu, Ya ;
- Fugui Fang ;
- Yunhai Zhang
GO analysis of predicted targets of lncRNAs in trans. (XLS 1551Â kb)
Authors
- Xiaoxiao Gao ;
- Ye, Jing ;
- Yang, Chen ;
- Kaifa Zhang ;
- Xiumei Li ;
- Luo, Lei ;
- Jianping Ding ;
- Yunsheng Li ;
- Hongguo Cao ;
- Yinghui Ling ;
- Xiaorong Zhang ;
- Liu, Ya ;
- Fugui Fang ;
- Yunhai Zhang