about
Allele-specific silencing of a pathogenic mutant acetylcholine receptor subunit by RNA interferenceTargeting blood-brain-barrier transcytosis - perspectives for drug deliveryPeptides for nucleic acid deliveryLipid-based Transfection Reagents Exhibit Cryo-induced Increase in Transfection Efficiency.Current understanding of molecular pathology and treatment of cardiomyopathy in duchenne muscular dystrophyExtracellular vesicle-mediated delivery of molecular compounds into gametes and embryos: learning from natureGenetic therapies for RNA mis-splicing diseasesIdentification of allele-specific RNAi effectors targeting genetic forms of Parkinson's diseaseSelective release of muscle-specific, extracellular microRNAs during myogenic differentiationUsing siRNA to define functional interactions between melanopsin and multiple G Protein partners.Prevention of exercised induced cardiomyopathy following Pip-PMO treatment in dystrophic mdx mice.Exosomes surf on filopodia to enter cells at endocytic hot spots, traffic within endosomes, and are targeted to the ERSeasonal variation in Plasmodium prevalence in a population of blue tits Cyanistes caeruleus.Design of RNAi hairpins for mutation-specific silencing of ataxin-7 and correction of a SCA7 phenotype.Context Dependent Effects of Chimeric Peptide Morpholino Conjugates Contribute to Dystrophin Exon-skipping EfficiencyIdentification of a Peptide for Systemic Brain Delivery of a Morpholino Oligonucleotide in Mouse Models of Spinal Muscular AtrophyThe role of long non-coding RNAs in neurodevelopment, brain function and neurological diseaseSplice-correcting oligonucleotides restore BTK function in X-linked agammaglobulinemia modelDNA cage delivery to mammalian cells.Systemic exosomal siRNA delivery reduced alpha-synuclein aggregates in brains of transgenic miceLearned kin recognition cues in a social bird.Allele-specific silencing of mutant Ataxin-7 in SCA7 patient-derived fibroblasts.Systemic peptide-mediated oligonucleotide therapy improves long-term survival in spinal muscular atrophy.Cross-talking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7Bi-specific splice-switching PMO oligonucleotides conjugated via a single peptide active in a mouse model of Duchenne muscular dystrophy.Pip5 transduction peptides direct high efficiency oligonucleotide-mediated dystrophin exon skipping in heart and phenotypic correction in mdx mice.Assessment of RT-qPCR normalization strategies for accurate quantification of extracellular microRNAs in murine serumExtracellular vesicle in vivo biodistribution is determined by cell source, route of administration and targeting.The acute inflammatory response to intranigral α-synuclein differs significantly from intranigral lipopolysaccharide and is exacerbated by peripheral inflammation.The biogenesis and characterization of mammalian microRNAs of mirtron origin.Correlating In Vitro Splice Switching Activity With Systemic In Vivo Delivery Using Novel ZEN-modified Oligonucleotides.How much dystrophin is enough: the physiological consequences of different levels of dystrophin in the mdx mouseSerum proteomic profiling reveals fragments of MYOM3 as potential biomarkers for monitoring the outcome of therapeutic interventions in muscular dystrophies.Delivering RNA interference to the mammalian brain.Multi-level omics analysis in a murine model of dystrophin loss and therapeutic restoration.Identification of novel, therapy-responsive protein biomarkers in a mouse model of Duchenne muscular dystrophy by aptamer-based serum proteomics.Dual Myostatin and Dystrophin Exon Skipping by Morpholino Nucleic Acid Oligomers Conjugated to a Cell-penetrating Peptide Is a Promising Therapeutic Strategy for the Treatment of Duchenne Muscular Dystrophy.Hexose enhances oligonucleotide delivery and exon skipping in dystrophin-deficient mdx mice.Modulating the expression of disease genes with RNA-based therapy.Improved cell-penetrating peptide-PNA conjugates for splicing redirection in HeLa cells and exon skipping in mdx mouse muscle.
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description
researcher
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wetenschapper
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name
Matthew J. Wood
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Wood MJ
@nl
type
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Matthew J. Wood
@en
Wood MJ
@nl
altLabel
Wood MJ
@en
prefLabel
Matthew J. Wood
@en
Wood MJ
@nl
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P106
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0000-0002-5436-6011