更正：杜兴氏肌肉营养不良犬模型中疾病进展的表达谱分析。
Correction: Expression profiling of disease progression in canine model of Duchenne muscular dystrophy.
作者信息
Brinkmeyer-Langford Candice, Chu Candice, Balog-Alvarez Cynthia, Yu Xue, Cai James J, Nabity Mary, Kornegay Joe N
出版信息
PLoS One. 2020 Jul 23;15(7):e0236916. doi: 10.1371/journal.pone.0236916. eCollection 2020.
Abstract
[This corrects the article DOI: 10.1371/journal.pone.0194485.].
摘要
[本文更正了文章的数字对象标识符：10.1371/journal.pone.0194485。]
相似文献
1
Correction: Expression profiling of disease progression in canine model of Duchenne muscular dystrophy.
PLoS One. 2020 Jul 23;15(7):e0236916. doi: 10.1371/journal.pone.0236916. eCollection 2020.
2
Correction: Challenges associated with homologous directed repair using CRISPR-Cas9 and TALEN to edit the DMD genetic mutation in canine Duchenne muscular dystrophy.
PLoS One. 2020 Oct 22;15(10):e0241430. doi: 10.1371/journal.pone.0241430. eCollection 2020.
3
Correction: Correction: Wild-Type Mouse Models to Screen Antisense Oligonucleotides for Exon-Skipping Efficacy in Duchenne Muscular Dystrophy.
PLoS One. 2019 Feb 20;14(2):e0212820. doi: 10.1371/journal.pone.0212820. eCollection 2019.
4
Correction: Discovery of Metabolic Biomarkers for Duchenne Muscular Dystrophy within a Natural History Study.
PLoS One. 2016 Jul 19;11(7):e0159895. doi: 10.1371/journal.pone.0159895. eCollection 2016.
5
Correction: Wild-Type Mouse Models to Screen Antisense Oligonucleotides for Exon-Skipping Efficacy in Duchenne Muscular Dystrophy.
PLoS One. 2018 Nov 15;13(11):e0207817. doi: 10.1371/journal.pone.0207817. eCollection 2018.
6
Correction: Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53.
PLoS One. 2019 Jul 31;14(7):e0220714. doi: 10.1371/journal.pone.0220714. eCollection 2019.
7
Canine X-linked muscular dystrophy as an animal model of Duchenne muscular dystrophy: a review.
Am J Med Genet. 1992 Feb 1;42(3):352-6. doi: 10.1002/ajmg.1320420320.
8
Determination of qPCR Reference Genes Suitable for Normalizing Gene Expression in a Canine Model of Duchenne Muscular Dystrophy.
J Neuromuscul Dis. 2018;5(2):177-191. doi: 10.3233/JND-170267.
9
Expression profiling of disease progression in canine model of Duchenne muscular dystrophy.
PLoS One. 2018 Mar 19;13(3):e0194485. doi: 10.1371/journal.pone.0194485. eCollection 2018.
10
Correction: Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan.
PLoS One. 2017 Aug 10;12(8):e0183406. doi: 10.1371/journal.pone.0183406. eCollection 2017.
引用本文的文献
1
Dystrophin-deficient muscular dystrophy in a Toy Poodle with a single base pair insertion in exon 45 of the Duchenne muscular dystrophy gene.
J Vet Med Sci. 2022 Apr 13;84(4):502-506. doi: 10.1292/jvms.21-0504. Epub 2022 Feb 8.
本文引用的文献
1
Expression profiling of disease progression in canine model of Duchenne muscular dystrophy.
PLoS One. 2018 Mar 19;13(3):e0194485. doi: 10.1371/journal.pone.0194485. eCollection 2018.
Zotero 插件