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. 2018 Nov 15;13(11):e0207817. doi: 10.1371/journal.pone.0207817

Correction: Wild-Type Mouse Models to Screen Antisense Oligonucleotides for Exon-Skipping Efficacy in Duchenne Muscular Dystrophy

Limin Cao, Gang Han, Ben Gu, HaiFang Yin
PMCID: PMC6237414  PMID: 30440030

S2 Fig contains incorrectly duplicated panels. The authors have provided a corrected version here.

Supporting information

S2 Fig. Routine hematoxylin and eosin staining for examining muscle morphology.

Hematoxylin and eosin staining of TA tissue sections from treated C57BL6 mice with 2 μg PMO, 5 μg PNA and 5 μg 2′Ome PS by local injection at different time-points e.g. 48 hr, 2 and 4 weeks after injection, and C57BL6 normal controls. Scale Bar = 100 μm. No difference was observed between treated and untreated mdx mice.

(TIF)

Reference

  • 1.Cao L, Han G, Gu B, Yin H (2014) Wild-Type Mouse Models to Screen Antisense Oligonucleotides for Exon-Skipping Efficacy in Duchenne Muscular Dystrophy. PLoS ONE 9(11): e111079 10.1371/journal.pone.0111079 [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

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Supplementary Materials

S2 Fig. Routine hematoxylin and eosin staining for examining muscle morphology.

Hematoxylin and eosin staining of TA tissue sections from treated C57BL6 mice with 2 μg PMO, 5 μg PNA and 5 μg 2′Ome PS by local injection at different time-points e.g. 48 hr, 2 and 4 weeks after injection, and C57BL6 normal controls. Scale Bar = 100 μm. No difference was observed between treated and untreated mdx mice.

(TIF)


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