scholarly article | Q13442814 |
P50 | author | Sue Fletcher | Q55590323 |
Chalermchai Mitrpant | Q56879268 | ||
P2093 | author name string | Francesco Muntoni | |
Steve D Wilton | |||
Abbie M Adams | |||
Penny L Meloni | |||
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The muscular dystrophies | Q77731754 | ||
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Splicing mosaic of the myophosphorylase gene due to a silent mutation in McArdle disease | Q79324054 | ||
Deletion of exon 16 of the dystrophin gene is not associated with disease | Q79568411 | ||
DMD pseudoexon mutations: splicing efficiency, phenotype, and potential therapy | Q80145954 | ||
Local dystrophin restoration with antisense oligonucleotide PRO051 | Q80412961 | ||
By-passing the nonsense mutation in the 4 CV mouse model of muscular dystrophy by induced exon skipping | Q82591542 | ||
Restoration of correct splicing in thalassemic pre-mRNA by antisense oligonucleotides | Q24561454 | ||
Splicing regulation: from a parts list of regulatory elements to an integrated splicing code | Q24642620 | ||
Antisense oligonucleotide induced exon skipping and the dystrophin gene transcript: cocktails and chemistries | Q27480935 | ||
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Transcriptome and genome conservation of alternative splicing events in humans and mice. | Q30753313 | ||
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Function and genetics of dystrophin and dystrophin-related proteins in muscle | Q34120764 | ||
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Muscular dystrophy into the new millennium | Q34682745 | ||
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How prevalent is functional alternative splicing in the human genome? | Q35640491 | ||
Experience and strategy for the molecular testing of Duchenne muscular dystrophy | Q35789975 | ||
Primary mouse myoblast purification, characterization, and transplantation for cell-mediated gene therapy | Q36534906 | ||
Altered splicing in prelamin A-associated premature aging phenotypes | Q36640178 | ||
Variation in sequence and organization of splicing regulatory elements in vertebrate genes | Q37591781 | ||
Functional analysis of 114 exon-internal AONs for targeted DMD exon skipping: indication for steric hindrance of SR protein binding sites | Q38317038 | ||
Towards a therapeutic inhibition of dystrophin exon 23 splicing in mdx mouse muscle induced by antisense oligoribonucleotides (splicomers): target sequence optimisation using oligonucleotide arrays | Q38336213 | ||
In situ transcription and splicing in the Balbiani ring 3 gene | Q39645223 | ||
Induction of exon skipping of the dystrophin transcript in lymphoblastoid cells by transfecting an antisense oligodeoxynucleotide complementary to an exon recognition sequence | Q41168085 | ||
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 oligonucleotides | Q45007187 | ||
P433 | issue | 8 | |
P304 | page(s) | 1418-1426 | |
P577 | publication date | 2009-03-17 | |
P1433 | published in | Molecular Therapy | Q15762400 |
P1476 | title | Rational design of antisense oligomers to induce dystrophin exon skipping | |
P478 | volume | 17 |