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A Drosophila model of Spinal Muscular Atrophy uncouples the snRNP biogenesis functions of survival motor neuron from locomotion and viability defects

The Spinal Muscular Atrophy (SMA) protein, survival motor neuron (SMN), functions in the biogenesis of small nuclear ribonucleoproteins (snRNPs). SMN has also been implicated in tissue-specific functions, however, it remains unclear which of these is important for the etiology of SMA. Smn null mutan...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Praveen, Kavita, Wen, Ying, Matera, A. Gregory
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2012
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3405901/
https://ncbi.nlm.nih.gov/pubmed/22813737
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.celrep.2012.05.014
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