| Details |
| Disease Name | Cerebral Amyloid Angiopathy, Familial |
| Nocoding RNA Name | hsa-miR-582-3p |
| Expression Pattern | mutated |
| Species | Homo sapiens |
| Detection Methods | Sanger sequencing,RT-QMPSF,RNA-binding protein immunoprecipitation etc. |
| Target | APP |
| Tissue | blood |
| Treatment | N/A |
| PubMed ID | 25828868 |
| Year | 2015 |
| Detail Description | We sequenced the 3’UTR of APP in 90 patients, we identified three sequence variants in four patients.miR-892b significantly downregulated APP expression, whereas the ΔTA variant blocked this effect. Interestingly, miR-582-3p caused an increase in APP expression only in the presence of the ΔTA variant. |
NSDNA: The Nervous System Disease NcRNAome Atlas
Contact wanglh211@163.com for inquiries and feedback
© All right reserved 2016