Automated Author ProfileC., Murdoch
C., Murdoch
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: 1.3 (sum of 2 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
Introduction. Micro-RNAs (miRNAs) participate in different biological processes, including fetal hypoxia. In this work we aimed to evaluate the existence of a miRNA differential expression profile in maternal blood of pregnancies affected with late-onset fetal growth restriction (LO-FGR). Methods. In a prospective study, a group of 35 fetuses were evaluated with Doppler ultrasound after 36 weeks. These included 15 fetuses with LO-FGR defined as fetal birth weight (BW) <10th centile plus a cerebroplacental ratio (CPR) <0,6765 MoM, and 20 normal fetuses (normal BW plus a normal CPR). Afterwards, for every pregnancy, maternal blood plasma was collected at birth, miRNAs were extracted, and full miRNA sequencing was performed using 20 of the indicated samples (12 with LO-FGR and 8 normal), determining the existence of differentially expressed miRNAs. Finally, this differential expression was validated in a wider population of 35 fetuses by means of RT-qPCR. Results. Full mRNA sequencing showed that FGR mothers expressed differential expression of several miRNA, The highest differences were seen for: miR-486-5p/3p, miR-516a/b-5p, miR-19a/b-3p, miR-296-5p, miR-10b-5p, miR-205-5p and Let-7g-5p. However, PCR validation only confirmed significant differences in miR-486-5p/3p. Conclusion. Mothers delivering FGR fetuses express a miRNA profile, which includes differential expression of miR-486-5p/3p. This information might improve our understanding of the pathophysiological processes involved in late-onset FGR.
Authors
- karger, figshare admin ;
- J., Morales-Roselló ;
- A.I., Martínez-Hernández ;
- J., Scheel ;
- G., Loscalzo ;
- E.M., García-López ;
- C., Murdoch
Introduction. Micro-RNAs (miRNAs) participate in different biological processes, including fetal hypoxia. In this work we aimed to evaluate the existence of a miRNA differential expression profile in maternal blood of pregnancies affected with late-onset fetal growth restriction (LO-FGR). Methods. In a prospective study, a group of 35 fetuses were evaluated with Doppler ultrasound after 36 weeks. These included 15 fetuses with LO-FGR defined as fetal birth weight (BW) <10th centile plus a cerebroplacental ratio (CPR) <0,6765 MoM, and 20 normal fetuses (normal BW plus a normal CPR). Afterwards, for every pregnancy, maternal blood plasma was collected at birth, miRNAs were extracted, and full miRNA sequencing was performed using 20 of the indicated samples (12 with LO-FGR and 8 normal), determining the existence of differentially expressed miRNAs. Finally, this differential expression was validated in a wider population of 35 fetuses by means of RT-qPCR. Results. Full mRNA sequencing showed that FGR mothers expressed differential expression of several miRNA, The highest differences were seen for: miR-486-5p/3p, miR-516a/b-5p, miR-19a/b-3p, miR-296-5p, miR-10b-5p, miR-205-5p and Let-7g-5p. However, PCR validation only confirmed significant differences in miR-486-5p/3p. Conclusion. Mothers delivering FGR fetuses express a miRNA profile, which includes differential expression of miR-486-5p/3p. This information might improve our understanding of the pathophysiological processes involved in late-onset FGR.
Authors
- karger, figshare admin ;
- J., Morales-Roselló ;
- A.I., Martínez-Hernández ;
- J., Scheel ;
- G., Loscalzo ;
- E.M., García-López ;
- C., Murdoch