The survival of motor neuron protein acts as a molecular chaperone for mRNP assembly

Spinal muscular atrophy (SMA) is a motor neuron disease caused by reduced levels of the survival of motor neuron (SMN) protein. SMN is part of a multiprotein complex that facilitates the assembly of spliceosomal small nuclear ribonucleoproteins (snRNPs). SMN has also been found to associate with mRN...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Cell Rep
Päätekijät: Donlin-Asp, Paul G., Fallini, Claudia, Campos, Jazmin, Chou, Ching-Chieh, Merritt, Megan E., Phan, Han C., Bassell, Gary J., Rossoll, Wilfried
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2017
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5492976/
https://ncbi.nlm.nih.gov/pubmed/28199839
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.celrep.2017.01.059
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