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A new cis-acting motif is required for the axonal SMN-dependent Anxa2 mRNA localization

Spinal muscular atrophy (SMA) is caused by mutations and/or deletions of the survival motor neuron gene (SMN1). Besides its function in the biogenesis of spliceosomal snRNPs, SMN might possess a motor neuron specific role and could function in the transport of axonal mRNAs and in the modulation of l...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:RNA
Päätekijät: Rihan, Khalil, Antoine, Etienne, Maurin, Thomas, Bardoni, Barbara, Bordonné, Rémy, Soret, Johann, Rage, Florence
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Cold Spring Harbor Laboratory Press 2017
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5435863/
https://ncbi.nlm.nih.gov/pubmed/28258160
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1261/rna.056788.116
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