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Deciphering miRNA transcription factor feed-forward loops to identify drug repurposing candidates for cystic fibrosis
BACKGROUND: Cystic fibrosis (CF) is a fatal genetic disorder caused by mutations in the CF transmembrane conductance regulator (CFTR) gene that primarily affects the lungs and the digestive system, and the current drug treatment is mainly able to alleviate symptoms. To improve disease management for...
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| Publicado no: | Genome Med |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4256829/ https://ncbi.nlm.nih.gov/pubmed/25484921 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-014-0094-2 |
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