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Lysine-Less Variants of Spinal Muscular Atrophy SMN and SMNΔ7 Proteins Are Degraded by the Proteasome Pathway

Spinal muscular atrophy is due to mutations affecting the SMN1 gene coding for the full-length protein (survival motor neuron; SMN) and the SMN2 gene that preferentially generates an exon 7-deleted protein (SMNΔ7) by alternative splicing. To study SMN and SMNΔ7 degradation in the cell, we have used...

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Bibliografske podrobnosti
izdano v:Int J Mol Sci
Main Authors: Sánchez-Lanzas, Raúl, Castaño, José G.
Format: Artigo
Jezik:Inglês
Izdano: MDPI 2017
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5751269/
https://ncbi.nlm.nih.gov/pubmed/29292768
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms18122667
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