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SMN is required for sensory-motor circuit function in Drosophila

Spinal muscular atrophy (SMA) is a lethal human disease characterized by motor neuron dysfunction and muscle deterioration due to depletion of the ubiquitous Survival Motor Neuron (SMN) protein. Drosophila SMN mutants have reduced muscle size and defective locomotion, motor rhythm and motor neuron n...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Imlach, Wendy L., Beck, Erin S., Choi, Ben Jiwon, Lotti, Francesco, Pellizzoni, Livio, McCabe, Brian D.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2012
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3475188/
https://ncbi.nlm.nih.gov/pubmed/23063130
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2012.09.011
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