Current status of pharmaceutical and genetic therapeutic approaches to treat DMD
Duchenne muscular dystrophy (DMD) is a genetic disease affecting about one in every 3,500 boys. This X-linked pathology is due to the absence of dystrophin in muscle fibers. This lack of dystrophin leads to the progressive muscle degeneration that is often responsible for the death of the DMD patien...
Asıl Yazarlar: | Pichavant, C, Aartsma-Rus, A, Clemens, P, Davies, K, Dickson, G, Takeda, S, Wilton, S, Wolff, J, Wooddell, C, Xiao, X, Tremblay, J |
---|---|
Materyal Türü: | Journal article |
Dil: | English |
Baskı/Yayın Bilgisi: |
2011
|
Benzer Materyaller
-
Current status of pharmaceutical and genetic therapeutic approaches to treat DMD.
Yazar:: Pichavant, C, ve diğerleri
Baskı/Yayın Bilgisi: (2011) -
Utrophin upregulation in DMD therapy: current status and new tools for the future
Yazar:: Fairclough, R, ve diğerleri
Baskı/Yayın Bilgisi: (2011) -
DMD antisense oligonucleotide mediated exon skipping efficiency correlates with flanking intron retention time and target position within the exon
Yazar:: Remko Goossens, ve diğerleri
Baskı/Yayın Bilgisi: (2023-12-01) -
BMP antagonists enhance myogenic differentiation and ameliorate the dystrophic phenotype in a DMD mouse model
Yazar:: SongTing Shi, ve diğerleri
Baskı/Yayın Bilgisi: (2011-02-01) -
DMD and West syndrome
Yazar:: Cardas, R, ve diğerleri
Baskı/Yayın Bilgisi: (2017)