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Genetic screen identifies a requirement for SMN in mRNA localisation within the Drosophila oocyte
OBJECTIVE: Spinal muscular atrophy (SMA) results from insufficient levels of the survival motor neuron (SMN) protein. Drosophila is conducive to large-scale genetic-modifier screens which can reveal novel pathways underpinning the disease mechanism. We tested the ability of a large collection of gen...
Gespeichert in:
| Veröffentlicht in: | BMC Res Notes |
|---|---|
| Hauptverfasser: | , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2018
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5998591/ https://ncbi.nlm.nih.gov/pubmed/29895323 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13104-018-3496-1 |
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