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Science Translational Medicine
|
April 29, 2010
Toward an oligonucleotide therapy for Duchenne muscular dystrophy: a complex development challenge
Matthew J A Wood
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
December 10, 2013
To skip or not to skip: that is the question for duchenne muscular dystrophy
Matthew J A Wood
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology
|
September 21, 2011
Exosome nanotechnology: an emerging paradigm shift in drug delivery: exploitation of exosome nanovesicles for systemic in vivo delivery of RNAi heralds new horizons for drug delivery across biological barriers
Samira Lakhal, Matthew J A Wood
Nature Reviews. Drug Discovery
|
August 2, 2011
Targeting RNA to treat neuromuscular disease
Francesco Muntoni, Matthew J A Wood
Molecular Biology of the Cell
|
October 24, 2008
Localization of double-stranded small interfering RNA to cytoplasmic processing bodies is Ago2 dependent and results in up-regulation of GW182 and Argonaute-2
Aarti Jagannath, Matthew J A Wood
Science Translational Medicine
|
September 27, 2019
Wrangling RNA: Antisense oligonucleotides for neurological disorders
Kevin Talbot, Matthew J A Wood
Trends in Genetics : TIG
|
December 8, 2009
Therapeutic gene silencing strategies for polyglutamine disorders
Janine Scholefield, Matthew J A Wood
Nature Reviews. Neurology
|
December 2, 2017
Antisense oligonucleotides: the next frontier for treatment of neurological disorders
Carlo Rinaldi, Matthew J A Wood
Journal of Neuromuscular Diseases
|
June 7, 2021
Emerging Oligonucleotide Therapeutics for Rare Neuromuscular Diseases
Yoshitsugu Aoki, Matthew J A Wood
Med (New York, N.Y.)
|
November 12, 2022
RNase-H-mediated silencing in the CNS proves predictably nontrivial
Michael P Moazami, Matthew J A Wood
Page
of 20
Search research articles
Search
Showing results (1-10 of 193) with videos related to
Sort By:
Page
of 20
Science Translational Medicine
|
April 29, 2010
Toward an oligonucleotide therapy for Duchenne muscular dystrophy: a complex development challenge
Matthew J A Wood
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
December 10, 2013
To skip or not to skip: that is the question for duchenne muscular dystrophy
Matthew J A Wood
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology
|
September 21, 2011
Exosome nanotechnology: an emerging paradigm shift in drug delivery: exploitation of exosome nanovesicles for systemic in vivo delivery of RNAi heralds new horizons for drug delivery across biological barriers
Samira Lakhal, Matthew J A Wood
Nature Reviews. Drug Discovery
|
August 2, 2011
Targeting RNA to treat neuromuscular disease
Francesco Muntoni, Matthew J A Wood
Molecular Biology of the Cell
|
October 24, 2008
Localization of double-stranded small interfering RNA to cytoplasmic processing bodies is Ago2 dependent and results in up-regulation of GW182 and Argonaute-2
Aarti Jagannath, Matthew J A Wood
Science Translational Medicine
|
September 27, 2019
Wrangling RNA: Antisense oligonucleotides for neurological disorders
Kevin Talbot, Matthew J A Wood
Trends in Genetics : TIG
|
December 8, 2009
Therapeutic gene silencing strategies for polyglutamine disorders
Janine Scholefield, Matthew J A Wood
Nature Reviews. Neurology
|
December 2, 2017
Antisense oligonucleotides: the next frontier for treatment of neurological disorders
Carlo Rinaldi, Matthew J A Wood
Journal of Neuromuscular Diseases
|
June 7, 2021
Emerging Oligonucleotide Therapeutics for Rare Neuromuscular Diseases
Yoshitsugu Aoki, Matthew J A Wood
Med (New York, N.Y.)
|
November 12, 2022
RNase-H-mediated silencing in the CNS proves predictably nontrivial
Michael P Moazami, Matthew J A Wood
Page
of 20