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Rational design of antisense oligomers to induce dystrophin exon skipping.Antisense oligonucleotide induction of progerin in human myogenic cellsPersonalised genetic intervention for Duchenne muscular dystrophy: antisense oligomers and exon skipping.Co-regulation of survival of motor neuron and Bcl-xL expression: implications for neuroprotection in spinal muscular atrophy.A novel morpholino oligomer targeting ISS-N1 improves rescue of severe spinal muscular atrophy transgenic miceComplement-mediated muscle cell lysis: a possible mechanism of myonecrosis in anti-SRP associated necrotizing myopathy (ASANM).Antisense Oligonucleotide-Mediated Terminal Intron Retention of the SMN2 Transcript.By-passing the nonsense mutation in the 4 CV mouse model of muscular dystrophy by induced exon skippingAnalysis of HLA-DRB3 alleles and supertypical genotypes in the MHC Class II region in sporadic inclusion body myositis
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onderzoeker
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հետազոտող
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