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George Dickson

Showing results (71-80 of 107) with videos related to

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Molecules (Basel, Switzerland)|January 26, 2012
Novel cationic carotenoid lipids as delivery vectors of antisense oligonucleotides for exon skipping in Duchenne muscular dystrophyLinda J Popplewell, Aseel Abu-Dayya, Tushar Khanna, et al.
Human Molecular Genetics|January 5, 2002
Acute regression of advanced and retardation of early aortic atheroma in immunocompetent apolipoprotein-E (apoE) deficient mice by administration of a second generation [E1(-), E3(-), polymerase(-)] adenovirus vector expressing human apoEJulian D Harris, Ian R Graham, Silke Schepelmann, et al.
Human Gene Therapy|February 4, 2014
Long-term episomal transgene expression from mitotically stable integration-deficient lentiviral vectorsHanna Kymäläinen, J Uwe Appelt, Frank A Giordano, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 7, 2011
Current status of pharmaceutical and genetic therapeutic approaches to treat DMDChristophe Pichavant, Annemieke Aartsma-Rus, Paula R Clemens, et al.
Rejuvenation Research|May 2, 2009
Adeno-associated virus-8-mediated intravenous transfer of myostatin propeptide leads to systemic functional improvements of slow but not fast muscleKeith Foster, Ian R Graham, Anthony Otto, et al.
Human Molecular Genetics|June 17, 2006
Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx miceKaori Ito, Shigemi Kimura, Shiro Ozasa, et al.
BMC Neurology|July 3, 2013
Nuclear entrapment and extracellular depletion of PCOLCE is associated with muscle degeneration in oculopharyngeal muscular dystrophyVered Raz, Ellen Sterrenburg, Samantha Routledge, et al.
Human Molecular Genetics|July 6, 2016
Antisense pre-treatment increases gene therapy efficacy in dystrophic musclesCécile Peccate, Amédée Mollard, Maëva Le Hir, et al.
Nucleic Acids Research|December 20, 2015
piggyBac transposons expressing full-length human dystrophin enable genetic correction of dystrophic mesoangioblastsMariana Loperfido, Susan Jarmin, Sumitava Dastidar, et al.
Journal of Cachexia, Sarcopenia and Muscle|February 8, 2020
Myostatin inhibition in combination with antisense oligonucleotide therapy improves outcomes in spinal muscular atrophyHaiyan Zhou, Jinhong Meng, Alberto Malerba, et al.
Pageof 11

Showing results (71-80 of 107) with videos related to

Sort By:
Pageof 11
Molecules (Basel, Switzerland)|January 26, 2012
Novel cationic carotenoid lipids as delivery vectors of antisense oligonucleotides for exon skipping in Duchenne muscular dystrophyLinda J Popplewell, Aseel Abu-Dayya, Tushar Khanna, et al.
Human Molecular Genetics|January 5, 2002
Acute regression of advanced and retardation of early aortic atheroma in immunocompetent apolipoprotein-E (apoE) deficient mice by administration of a second generation [E1(-), E3(-), polymerase(-)] adenovirus vector expressing human apoEJulian D Harris, Ian R Graham, Silke Schepelmann, et al.
Human Gene Therapy|February 4, 2014
Long-term episomal transgene expression from mitotically stable integration-deficient lentiviral vectorsHanna Kymäläinen, J Uwe Appelt, Frank A Giordano, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 7, 2011
Current status of pharmaceutical and genetic therapeutic approaches to treat DMDChristophe Pichavant, Annemieke Aartsma-Rus, Paula R Clemens, et al.
Rejuvenation Research|May 2, 2009
Adeno-associated virus-8-mediated intravenous transfer of myostatin propeptide leads to systemic functional improvements of slow but not fast muscleKeith Foster, Ian R Graham, Anthony Otto, et al.
Human Molecular Genetics|June 17, 2006
Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx miceKaori Ito, Shigemi Kimura, Shiro Ozasa, et al.
BMC Neurology|July 3, 2013
Nuclear entrapment and extracellular depletion of PCOLCE is associated with muscle degeneration in oculopharyngeal muscular dystrophyVered Raz, Ellen Sterrenburg, Samantha Routledge, et al.
Human Molecular Genetics|July 6, 2016
Antisense pre-treatment increases gene therapy efficacy in dystrophic musclesCécile Peccate, Amédée Mollard, Maëva Le Hir, et al.
Nucleic Acids Research|December 20, 2015
piggyBac transposons expressing full-length human dystrophin enable genetic correction of dystrophic mesoangioblastsMariana Loperfido, Susan Jarmin, Sumitava Dastidar, et al.
Journal of Cachexia, Sarcopenia and Muscle|February 8, 2020
Myostatin inhibition in combination with antisense oligonucleotide therapy improves outcomes in spinal muscular atrophyHaiyan Zhou, Jinhong Meng, Alberto Malerba, et al.
Pageof 11