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Genome-wide identification of mRNAs associated with the protein SMN whose depletion decreases their axonal localization
Spinal muscular atrophy is a neuromuscular disease resulting from mutations in the SMN1 gene, which encodes the survival motor neuron (SMN) protein. SMN is part of a large complex that is essential for the biogenesis of spliceosomal small nuclear RNPs. SMN also colocalizes with mRNAs in granules tha...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3884661/ https://ncbi.nlm.nih.gov/pubmed/24152552 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1261/rna.040204.113 |
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