Lysosomal dysfunction increases exosome-mediated alpha-synuclein release and transmission von Alvarez-Erviti, Lydia, Seow, Yiqi, Schapira, Anthony H, Gardiner, Chris, Sargent, Ian L, Wood, Matthew J.A, Cooper, J. Mark

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The CRTC1-SIK1 Pathway Regulates Entrainment of the Circadian Clock von Jagannath, Aarti, Butler, Rachel, Godinho, Sofia I.H., Couch, Yvonne, Brown, Laurence A., Vasudevan, Sridhar R., Flanagan, Kevin C., Anthony, Daniel, Churchill, Grant C., Wood, Matthew J.A., Steiner, Guido, Ebeling, Martin, Hossbach, Markus, Wettstein, Joseph G., Duffield, Giles E., Gatti, Silvia, Hankins, Mark W., Foster, Russell G., Peirson, Stuart N.

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Peptide-conjugate antisense based splice-correction for Duchenne muscular dystrophy and other neuromuscular diseases von Tsoumpra, Maria K., Fukumoto, Seiji, Matsumoto, Toshio, Takeda, Shin'ichi, Wood, Matthew J.A., Aoki, Yoshitsugu

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Extracellular vesicles: emerging targets for cancer therapy von Vader, Pieter, Breakefield, Xandra O, Wood, Matthew J.A

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Extracellular vesicles: biology and emerging therapeutic opportunities von EL Andaloussi, Samir, Mäger, Imre, Breakefield, Xandra O., Wood, Matthew J. A.

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Localization of double-stranded small interfering RNA to cytoplasmic processing bodies is Ago2 dependent and results in up-regulation of GW182 and Argonaute-2 von Jagannath, Aarti, Wood, Matthew J A

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Delivery of siRNA to the mouse brain by systemic injection of targeted exosomes von Wood, Matthew J A, Alvarez-Erviti, Lydia, Seow, Yiqi, Yin, HaiFang, Betts, Corinne, Lakhal, Samira

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Electroporation-induced siRNA precipitation obscures the efficiency of siRNA loading into extracellular vesicles von Kooijmans, Sander A.A., Stremersch, Stephan, Braeckmans, Kevin, de Smedt, Stefaan C., Hendrix, An, Wood, Matthew J.A., Schiffelers, Raymond M., Raemdonck, Koen, Vader, Pieter

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Uniform sarcolemmal dystrophin expression is required to prevent extracellular microRNA release and improve dystrophic pathology von Westering, Tirsa L.E., Lomonosova, Yulia, Coenen‐Stass, Anna M.L., Betts, Corinne A., Bhomra, Amarjit, Hulsker, Margriet, Clark, Lucy E., McClorey, Graham, Aartsma‐Rus, Annemieke, Putten, Maaike, Wood, Matthew J.A., Roberts, Thomas C.

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Exosome-mediated delivery of siRNA in vitro and in vivo von El-Andaloussi, Samir, Lee, Yi, Lakhal-Littleton, Samira, Li, Jinghuan, Seow, Yiqi, Gardiner, Chris, Alvarez-Erviti, Lydia, Sargent, Ian L, Wood, Matthew J A

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Peptide-conjugated oligonucleotides evoke long-lasting myotonic dystrophy correction in patient-derived cells and mice von Klein, Arnaud F, Varela, Miguel A, Arandel, Ludovic, Holland, Ashling, Naouar, Naira, Arzumanov, Andrey, Seoane, David, Revillod, Lucile, Bassez, Guillaume, Ferry, Arnaud, Jauvin, Dominic, Gourdon, Genevieve, Puymirat, Jack, Gait, Michael J, Furling, Denis, Wood, Matthew Ja

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Functional Delivery of Lipid-Conjugated siRNA by Extracellular Vesicles von O’Loughlin, Aisling J., Mäger, Imre, de Jong, Olivier G., Varela, Miguel A., Schiffelers, Raymond M., El Andaloussi, Samir, Wood, Matthew J.A., Vader, Pieter

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Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomers von Goyenvalle, Aurélie, Griffith, Graziella, Babbs, Arran, Andaloussi, Samir El, Ezzat, Kariem, Avril, Aurélie, Dugovic, Branislav, Chaussenot, Rémi, Ferry, Arnaud, Voit, Thomas, Amthor, Helge, Bühr, Claudia, Schürch, Stefan, Wood, Matthew J A, Davies, Kay E, Vaillend, Cyrille, Leumann, Christian, Garcia, Luis

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Biomarker Potential of Extracellular miRNAs in Duchenne Muscular Dystrophy von Coenen-Stass, Anna M.L., Wood, Matthew J.A., Roberts, Thomas C.

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Targeting blood-brain-barrier transcytosis – perspectives for drug delivery von Mäger, Imre, Meyer, Axel H., Li, Jinghuan, Lenter, Martin, Hildebrandt, Tobias, Leparc, German, Wood, Matthew J.A.

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Therapeutic gene silencing strategies for polyglutamine disorders von Scholefield, Janine, Wood, Matthew J.A

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Heterogeneity and interplay of the extracellular vesicle small RNA transcriptome and proteome von Sork, Helena, Corso, Giulia, Krjutskov, Kaarel, Johansson, Henrik J., Nordin, Joel Z., Wiklander, Oscar P. B., Lee, Yi Xin Fiona, Westholm, Jakub Orzechowski, Lehtiö, Janne, Wood, Matthew J. A., Mäger, Imre, EL Andaloussi, Samir

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Genetic therapies for RNA mis-splicing diseases von Hammond, Suzan M, Wood, Matthew J.A

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Targeting RNA to treat neuromuscular disease von Muntoni, Francesco, Wood, Matthew J. A

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Cell-Penetrating Peptide Conjugates of Steric Blocking Oligonucleotides as Therapeutics for Neuromuscular Diseases from a Historical Perspective to Current Prospects of Treatment von Gait, Michael J., Arzumanov, Andrey A., McClorey, Graham, Godfrey, Caroline, Betts, Corinne, Hammond, Suzan, Wood, Matthew J.A.

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