Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse
about
Nanoparticle delivery of antisense oligonucleotides and their application in the exon skipping strategy for Duchenne muscular dystrophyEmerging genetic therapies to treat Duchenne muscular dystrophyAnti-tumor activity of splice-switching oligonucleotides.Restoring dystrophin expression in duchenne muscular dystrophy muscle progress in exon skipping and stop codon read through.Effective Delivery of PEGylated siRNA-Containing Lipoplexes to Extraperitoneal Tumours following Intraperitoneal Administration.Novel compounds for the treatment of Duchenne muscular dystrophy: emerging therapeutic agentsAntisense drug discovery and development.New developments in the use of gene therapy to treat Duchenne muscular dystrophy.Exon-skipping antisense oligonucleotides to correct missplicing in neurogenetic diseases.Pluronic-PEI copolymers enhance exon-skipping of 2'-O-methyl phosphorothioate oligonucleotide in cell culture and dystrophic mdx mice.Antisense Oligonucleotide-Based Therapy for Neuromuscular Disease.Translational development of splice-modifying antisense oligomers.Targeting Splicing in the Treatment of Human DiseaseNanotherapy for Duchenne muscular dystrophy.Accurate quantification of dystrophin mRNA and exon skipping levels in duchenne muscular dystrophy.Biodistribution studies of polymeric nanoparticles for drug delivery in mice.Persistent dystrophin protein restoration 90 days after a course of intraperitoneally administered naked 2'OMePS AON and ZM2 NP-AON complexes in mdx mice.Antisense mediated exon skipping therapy for duchenne muscular dystrophy (DMD)Biodistribution and molecular studies on orally administered nanoparticle-AON complexes encapsulated with alginate aiming at inducing dystrophin rescue in mdx mice.Dystrophin restoration in skeletal, heart and skin arrector pili smooth muscle of mdx mice by ZM2 NP-AON complexes.Encapsulation of Piper cabralanum (Piperaceae) nonpolar extract in poly(methyl methacrylate) by miniemulsion and evaluation of increase in the effectiveness of antileukemic activity in K562 cells.
P2860
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P2860
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse
description
2009 nî lūn-bûn
@nan
2009 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Cationic PMMA nanoparticles bi ...... in expression in the mdx mouse
@ast
Cationic PMMA nanoparticles bi ...... in expression in the mdx mouse
@en
type
label
Cationic PMMA nanoparticles bi ...... in expression in the mdx mouse
@ast
Cationic PMMA nanoparticles bi ...... in expression in the mdx mouse
@en
prefLabel
Cationic PMMA nanoparticles bi ...... in expression in the mdx mouse
@ast
Cationic PMMA nanoparticles bi ...... in expression in the mdx mouse
@en
P2093
P2860
P50
P356
P1433
P1476
Cationic PMMA nanoparticles bi ...... in expression in the mdx mouse
@en
P2093
Alessandra Ferlini
Alessandro Medici
Daniela Perrone
Elena Bassi
Elena Martoni
Francesca Gualandi
Giuliano Tomelleri
Marcella Neri
Marina Fabris
P2860
P304
P356
10.1038/MT.2009.8
P50
P577
2009-02-24T00:00:00Z