Rational design of antisense oligomers to induce dystrophin exon skipping.

scientific article

Rational design of antisense oligomers to induce dystrophin exon skipping. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1038/MT.2009.49
P932PMC publication ID2835229
P698PubMed publication ID19293776
P5875ResearchGate publication ID24207850

P50authorSue FletcherQ55590323
Chalermchai MitrpantQ56879268
P2093author name stringFrancesco Muntoni
Steve D Wilton
Abbie M Adams
Penny L Meloni
P2860cites workAntisense oligonucleotide-induced exon skipping restores dystrophin expression in vitro in a canine model of DMD.Q45858623
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Deletion of exon 16 of the dystrophin gene is not associated with diseaseQ79568411
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Local dystrophin restoration with antisense oligonucleotide PRO051Q80412961
By-passing the nonsense mutation in the 4 CV mouse model of muscular dystrophy by induced exon skippingQ82591542
Restoration of correct splicing in thalassemic pre-mRNA by antisense oligonucleotidesQ24561454
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Antisense oligonucleotide induced exon skipping and the dystrophin gene transcript: cocktails and chemistriesQ27480935
Mechanisms of alternative pre-messenger RNA splicingQ28131822
Comprehensive proteomic analysis of the human spliceosomeQ28201545
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An increased specificity score matrix for the prediction of SF2/ASF-specific exonic splicing enhancersQ33249150
Function and genetics of dystrophin and dystrophin-related proteins in muscleQ34120764
The architecture of pre-mRNAs affects mechanisms of splice-site pairing.Q34132523
The spliceosome: the most complex macromolecular machine in the cell?Q34278742
Rules of engagement: co-transcriptional recruitment of pre-mRNA processing factorsQ34419716
Protein composition of human prespliceosomes isolated by a tobramycin affinity-selection methodQ34429680
Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouseQ34582428
The influence of antisense oligonucleotide length on dystrophin exon skipping.Q34590393
Muscular dystrophy into the new millenniumQ34682745
Induction of revertant fibres in the mdx mouse using antisense oligonucleotidesQ34691050
How prevalent is functional alternative splicing in the human genome?Q35640491
Experience and strategy for the molecular testing of Duchenne muscular dystrophyQ35789975
Primary mouse myoblast purification, characterization, and transplantation for cell-mediated gene therapyQ36534906
Altered splicing in prelamin A-associated premature aging phenotypesQ36640178
Variation in sequence and organization of splicing regulatory elements in vertebrate genesQ37591781
Functional analysis of 114 exon-internal AONs for targeted DMD exon skipping: indication for steric hindrance of SR protein binding sitesQ38317038
Towards a therapeutic inhibition of dystrophin exon 23 splicing in mdx mouse muscle induced by antisense oligoribonucleotides (splicomers): target sequence optimisation using oligonucleotide arraysQ38336213
In situ transcription and splicing in the Balbiani ring 3 geneQ39645223
Induction of exon skipping of the dystrophin transcript in lymphoblastoid cells by transfecting an antisense oligodeoxynucleotide complementary to an exon recognition sequenceQ41168085
Target selection for antisense oligonucleotide induced exon skipping in the dystrophin gene.Q44471855
Targeted exon skipping in transgenic hDMD mice: A model for direct preclinical screening of human-specific antisense oligonucleotidesQ45007187
P433issue8
P304page(s)1418-1426
P577publication date2009-03-17
P1433published inMolecular TherapyQ15762400
P1476titleRational design of antisense oligomers to induce dystrophin exon skipping
P478volume17