Immortalized Muscle Cell Model to Test the Exon Skipping Efficacy for Duchenne Muscular Dystrophy-Reference-Cited by-同舟云学术

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Immortalized Muscle Cell Model to Test the Exon Skipping Efficacy for Duchenne Muscular Dystrophy

Published:2017-10-16 Issue:4 Volume:7 Page:13
ISSN:2075-4426
Container-title:Journal of Personalized Medicine
language:en
Short-container-title:JPM

Author:

Nguyen Quynh,Yokota Toshifumi^ORCID

Publisher

MDPI AG

Subject

Medicine (miscellaneous)

Link

http://www.mdpi.com/2075-4426/7/4/13/pdf

Reference62 articles.

1. Population frequencies of inherited neuromuscular diseases—A world survey

2. Dystrophin: The protein product of the duchenne muscular dystrophy locus

3. Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

4. Potential of oligonucleotide-mediated exon-skipping therapy for Duchenne muscular dystrophy

5. Improved diagnosis of Becker muscular dystrophy by dystrophin testing

Cited by 32 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Effects of local reduction of endogenous α-synuclein using antisense oligonucleotides on the fibril-induced propagation of pathology through the neural network in wild-type mice;Acta Neuropathologica Communications;2024-05-14

2. Production of Duchenne muscular dystrophy cellular model using CRISPR-Cas9 exon deletion strategy;Molecular and Cellular Biochemistry;2023-06-08

3. Exons 45–55 Skipping Using Antisense Oligonucleotides in Immortalized Human DMD Muscle Cells;Methods in Molecular Biology;2023

4. Automatic quantification of living cells via a non-invasive achromatic colorimetric sensor through machine learning-assisted image analysis using a smartphone;Chemical Engineering Journal;2022-12

5. Isolation and Characterization of Primary DMD Pig Muscle Cells as an In Vitro Model for Preclinical Research on Duchenne Muscular Dystrophy;Life;2022-10-21

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