Evaluation of potential effects of Plastin 3 overexpression and low-dose SMN-antisense oligonucleotides on putative biomarkers in spinal muscular atrophy mice

OBJECTIVES: Spinal muscular atrophy (SMA) is a devastating motor neuron disorder caused by homozygous loss of the survival motor neuron 1 (SMN1) gene and insufficient functional SMN protein produced by the SMN2 copy gene. Additional genetic protective modifiers such as Plastin 3 (PLS3) can counterac...

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Detalles Bibliográficos
Autores principales: Strathmann, Eike A., Peters, Miriam, Hosseinibarkooie, Seyyedmohsen, Rigo, Frank W., Bennett, C. Frank, Zaworski, Phillip G., Chen, Karen S., Nothnagel, Michael, Wirth, Brunhilde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126849/
https://www.ncbi.nlm.nih.gov/pubmed/30188931
http://dx.doi.org/10.1371/journal.pone.0203398

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126849/
https://www.ncbi.nlm.nih.gov/pubmed/30188931
http://dx.doi.org/10.1371/journal.pone.0203398

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