Literature DB >> 30440030

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.   

Abstract

[This corrects the article DOI: 10.1371/journal.pone.0111079.].

Entities:  

Year:  2018        PMID: 30440030      PMCID: PMC6237414          DOI: 10.1371/journal.pone.0207817

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


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

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) Click here for additional data file.
  1 in total

1.  Wild-type mouse models to screen antisense oligonucleotides for exon-skipping efficacy in Duchenne muscular dystrophy.

Authors:  Limin Cao; Gang Han; Ben Gu; HaiFang Yin
Journal:  PLoS One       Date:  2014-11-03       Impact factor: 3.240

  1 in total

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