© 2016, Springer Science+Business Media New York.Due to lack of effective therapies, muscular dystrophies became a focus for gene therapy. Multiple pre-clinical studies have shown successful restoration of dystrofin and dysferlin by RNA editing both in vivo and in vitro, but possibility of a clinical translation is still obscure. A number of new chemicals are being studied, and a search for new techniques is ongoing. This work is intended to give a brief overview of the current state of the RNA editing for treating muscular dystrophies
The exquisitely precise and co-ordinated process of gene transcript splicing, that is, intron remov...
Duchenne muscular dystrophy (DMD) is a genetic disease affecting about one in every 3,500 boys. This...
Dystrophia myotonica (DM1), one of the most common forms of muscular dystrophy, is caused by a repea...
Due to lack of effective therapies, muscular dystrophies became a focus for gene therapy. Multiple p...
Muscular dystrophies are a heterogeneous group of genetic disorders characterized by muscle weakness...
The identification of the Duchenne muscular dystrophy gene and protein in the late 1980s led to high...
Muscular dystrophies comprise a heterogeneous cluster of inherited muscle degenerative disorders wit...
ABSTRACTIntroduction: Exon skipping compounds restoring the dystrophin transcript reading frame have...
Introduction Exon skipping compounds restoring the dystrophin transcript reading frame have received...
AbstractDuchenne muscular dystrophy (DMD) is a progressive muscle degenerative disease affecting one...
stablishing dystrophin as the mutated gene in Duchenne muscular dystro-phy (DMD) was arguably the fi...
Duchenne muscular dystrophy (DMD), the most common and severe form of childhood muscle wasting, is m...
Splice-modulation therapy, whereby molecular manipulation of premessenger RNA splicing is engineered...
We are developing an alternative therapy for Duchenne muscular dystrophy (DMD) using antisense oligo...
Background. Antisense oligonucleotides can redirect the pre-mRNA processing of targeted gene transcr...
The exquisitely precise and co-ordinated process of gene transcript splicing, that is, intron remov...
Duchenne muscular dystrophy (DMD) is a genetic disease affecting about one in every 3,500 boys. This...
Dystrophia myotonica (DM1), one of the most common forms of muscular dystrophy, is caused by a repea...
Due to lack of effective therapies, muscular dystrophies became a focus for gene therapy. Multiple p...
Muscular dystrophies are a heterogeneous group of genetic disorders characterized by muscle weakness...
The identification of the Duchenne muscular dystrophy gene and protein in the late 1980s led to high...
Muscular dystrophies comprise a heterogeneous cluster of inherited muscle degenerative disorders wit...
ABSTRACTIntroduction: Exon skipping compounds restoring the dystrophin transcript reading frame have...
Introduction Exon skipping compounds restoring the dystrophin transcript reading frame have received...
AbstractDuchenne muscular dystrophy (DMD) is a progressive muscle degenerative disease affecting one...
stablishing dystrophin as the mutated gene in Duchenne muscular dystro-phy (DMD) was arguably the fi...
Duchenne muscular dystrophy (DMD), the most common and severe form of childhood muscle wasting, is m...
Splice-modulation therapy, whereby molecular manipulation of premessenger RNA splicing is engineered...
We are developing an alternative therapy for Duchenne muscular dystrophy (DMD) using antisense oligo...
Background. Antisense oligonucleotides can redirect the pre-mRNA processing of targeted gene transcr...
The exquisitely precise and co-ordinated process of gene transcript splicing, that is, intron remov...
Duchenne muscular dystrophy (DMD) is a genetic disease affecting about one in every 3,500 boys. This...
Dystrophia myotonica (DM1), one of the most common forms of muscular dystrophy, is caused by a repea...