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George Dickson

Showing results (21-30 of 107) with videos related to

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Expert Opinion on Biological Therapy|June 17, 2009
Gene therapy for muscular dystrophy: current progress and future prospectsCapucine Trollet, Takis Athanasopoulos, Linda Popplewell, et al.
Human Molecular Genetics|April 4, 2002
Adeno-associated virus vector gene transfer and sarcolemmal expression of a 144 kDa micro-dystrophin effectively restores the dystrophin-associated protein complex and inhibits myofibre degeneration in nude/mdx miceStewart A Fabb, Dominic J Wells, Patricia Serpente, et al.
Human Molecular Genetics|May 14, 2021
Systemic antisense therapeutics inhibiting DUX4 expression ameliorates FSHD-like pathology in an FSHD mouse modelNgoc Lu-Nguyen, Alberto Malerba, Shan Herath, et al.
Human Gene Therapy|November 29, 2016
Chimeric Trojan Protein Insertion in Lentiviral Membranes Makes Lentiviruses Susceptible to Neutralization by Anti-Tetanus Serum AntibodiesAnita Le Heron, Steven Patterson, Rafael J Yáñez-Muñoz, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 7, 2010
Antisense-induced myostatin exon skipping leads to muscle hypertrophy in mice following octa-guanidine morpholino oligomer treatmentJagjeet K Kang, Alberto Malerba, Linda Popplewell, et al.
Methods in Molecular Biology (Clifton, N.J.)|October 29, 2011
Gene therapy in skeletal muscle mediated by adeno-associated virus vectorsChunping Qiao, Taeyoung Koo, Juan Li, et al.
The Journal of Gene Medicine|December 7, 2011
Long-term functional adeno-associated virus-microdystrophin expression in the dystrophic CXMDj dogTaeyoung Koo, Takashi Okada, Takis Athanasopoulos, et al.
Immunology Letters|December 15, 2007
Activity of different vaccine-associated promoter elements in human dendritic cellsTimoleon Papagatsias, George Rozis, Takis Athanasopoulos, et al.
Journal of Molecular Neuroscience : MN|March 23, 2005
Correction of the neuropathogenic human apolipoprotein E4 (APOE4) gene to APOE3 in vitro using synthetic RNA/DNA oligonucleotides (chimeraplasts)Aristides D Tagalakis, J George Dickson, James S Owen, et al.
Human Gene Therapy|January 26, 2022
Improving Molecular and Histopathology in Diaphragm Muscle of the Double Transgenic ACTA1-MCM/FLExDUX4 Mouse Model of FSHD with Systemic Antisense TherapyNgoc Lu-Nguyen, Alberto Malerba, Marina Antoni Pineda, et al.
Pageof 11

Showing results (21-30 of 107) with videos related to

Sort By:
Pageof 11
Expert Opinion on Biological Therapy|June 17, 2009
Gene therapy for muscular dystrophy: current progress and future prospectsCapucine Trollet, Takis Athanasopoulos, Linda Popplewell, et al.
Human Molecular Genetics|April 4, 2002
Adeno-associated virus vector gene transfer and sarcolemmal expression of a 144 kDa micro-dystrophin effectively restores the dystrophin-associated protein complex and inhibits myofibre degeneration in nude/mdx miceStewart A Fabb, Dominic J Wells, Patricia Serpente, et al.
Human Molecular Genetics|May 14, 2021
Systemic antisense therapeutics inhibiting DUX4 expression ameliorates FSHD-like pathology in an FSHD mouse modelNgoc Lu-Nguyen, Alberto Malerba, Shan Herath, et al.
Human Gene Therapy|November 29, 2016
Chimeric Trojan Protein Insertion in Lentiviral Membranes Makes Lentiviruses Susceptible to Neutralization by Anti-Tetanus Serum AntibodiesAnita Le Heron, Steven Patterson, Rafael J Yáñez-Muñoz, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 7, 2010
Antisense-induced myostatin exon skipping leads to muscle hypertrophy in mice following octa-guanidine morpholino oligomer treatmentJagjeet K Kang, Alberto Malerba, Linda Popplewell, et al.
Methods in Molecular Biology (Clifton, N.J.)|October 29, 2011
Gene therapy in skeletal muscle mediated by adeno-associated virus vectorsChunping Qiao, Taeyoung Koo, Juan Li, et al.
The Journal of Gene Medicine|December 7, 2011
Long-term functional adeno-associated virus-microdystrophin expression in the dystrophic CXMDj dogTaeyoung Koo, Takashi Okada, Takis Athanasopoulos, et al.
Immunology Letters|December 15, 2007
Activity of different vaccine-associated promoter elements in human dendritic cellsTimoleon Papagatsias, George Rozis, Takis Athanasopoulos, et al.
Journal of Molecular Neuroscience : MN|March 23, 2005
Correction of the neuropathogenic human apolipoprotein E4 (APOE4) gene to APOE3 in vitro using synthetic RNA/DNA oligonucleotides (chimeraplasts)Aristides D Tagalakis, J George Dickson, James S Owen, et al.
Human Gene Therapy|January 26, 2022
Improving Molecular and Histopathology in Diaphragm Muscle of the Double Transgenic ACTA1-MCM/FLExDUX4 Mouse Model of FSHD with Systemic Antisense TherapyNgoc Lu-Nguyen, Alberto Malerba, Marina Antoni Pineda, et al.
Pageof 11