Non-uniform dystrophin re-expression after CRISPR-mediated exon excision in the dystrophin/utrophin double-knockout mouse model of DMD
<div>Duchenne muscular dystrophy (DMD) is the most prevalent inherited myopathy affecting children, caused by genetic loss of the gene encoding the dystrophin protein. Here we have investigated the use of the <em>Staphylococcus aureus</em> CRISPR-Cas9 system and a...
Asıl Yazarlar: | Hanson, B, Stenler, S, Ahlskog, N, Chwalenia, K, Svrzikapa, N, Coenen-Stass, AML, Weinberg, MS, Wood, MJA, Roberts, TC |
---|---|
Materyal Türü: | Journal article |
Dil: | English |
Baskı/Yayın Bilgisi: |
Cell Press
2022
|
Benzer Materyaller
-
Non-uniform dystrophin re-expression after CRISPR-mediated exon excision in the dystrophin/utrophin double-knockout mouse model of DMD
Yazar:: Britt Hanson, ve diğerleri
Baskı/Yayın Bilgisi: (2022-12-01) -
Exon skipping induces uniform dystrophin rescue with dose-dependent restoration of serum miRNA biomarkers and muscle biophysical properties
Yazar:: Chwalenia, K, ve diğerleri
Baskı/Yayın Bilgisi: (2022) -
Marginal level dystrophin expression improves clinical outcome in a strain of dystrophin/utrophin double knockout mice.
Yazar:: Dejia Li, ve diğerleri
Baskı/Yayın Bilgisi: (2010-12-01) -
Immunogold confirmation that utrophin is localized to the normal position of dystrophin in dystrophin-negative transgenic mouse muscle.
Yazar:: Culle, M, ve diğerleri
Baskı/Yayın Bilgisi: (2001) -
Rescu of severely affected dystrophin/utrophin deficient mice by morpholino-oligomer mediated exon skipping
Yazar:: Goyenvalle, A, ve diğerleri
Baskı/Yayın Bilgisi: (2010)