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Nature Communications, ISSN 2041-1723, 02/2017, Volume 8, Issue 1, p. 14454
Gene replacement therapies utilizing adeno-associated viral (AAV) vectors hold great promise for treating Duchenne muscular dystrophy (DMD). A related approach... 
CRISPR-CAS9 | SKELETAL | EXPRESSION | VECTORS | MULTIDISCIPLINARY SCIENCES | MDX MICE
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2018, Volume 13, Issue 2, p. e0193289
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/2010, Volume 107, Issue 44, pp. 19079 - 19083
Journal Article
Journal Article
Nature Medicine, ISSN 1078-8956, 2015, Volume 21, Issue 3, pp. 270 - 275
Journal Article
FASEB JOURNAL, ISSN 0892-6638, 07/2019, Volume 33, Issue 7, pp. 8110 - 8124
The C57BL/10ScSn-Dmd(mdx)/J (BL10-mdx) mouse has been the most commonly used model for Duchenne muscular dystrophy (DMD) for decades. Their muscle dysfunction... 
MDX MOUSE | pathology | regeneration | BIOCHEMISTRY & MOLECULAR BIOLOGY | PHENOTYPE | SATELLITE CELLS | muscle function | CELL BIOLOGY | GENE | BIOLOGY | fibrosis | MICE | calcification | Research
Journal Article