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Methods in Molecular Biology (Clifton, N.J.)
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November 18, 2022
Systemic Delivery of a Monoclonal Antibody to Immunologically Block Myostatin in the A17 Mouse Model of OPMD
Alberto Malerba, Pradeep Harish, Linda Popplewell
Expert Opinion on Biological Therapy
|
May 22, 2018
The progress of AAV-mediated gene therapy in neuromuscular disorders
Sara Aguti, Alberto Malerba, Haiyan Zhou
Nucleic Acid Therapeutics
|
August 20, 2011
Long-term systemic administration of unconjugated morpholino oligomers for therapeutic expression of dystrophin by exon skipping in skeletal muscle: implications for cardiac muscle integrity
Alberto Malerba, Luisa Boldrin, George Dickson
Methods in Molecular Biology (Clifton, N.J.)
|
September 2, 2018
Systemic Intravenous Administration of Antisense Therapeutics for Combinatorial Dystrophin and Myostatin Exon Splice Modulation
Ngoc Lu-Nguyen, George Dickson, Alberto Malerba
Methods in Molecular Biology (Clifton, N.J.)
|
July 28, 2025
Systemic Intravenous Administration of Antisense Therapeutics for Combinatorial Dystrophin and Myostatin Exon Splice Modulation
Ngoc Lu-Nguyen, George Dickson, Alberto Malerba
Methods in Molecular Biology (Clifton, N.J.)
|
March 29, 2012
Optimizing antisense oligonucleotides using phosphorodiamidate morpholino oligomers
Linda J Popplewell, Alberto Malerba, George Dickson
Nucleic Acid Therapeutics
|
July 31, 2020
Researcher's Perceptions on Publishing "Negative" Results and Open Access
Lucía Echevarría, Alberto Malerba, Virginia Arechavala-Gomeza
Methods in Molecular Biology (Clifton, N.J.)
|
February 25, 2022
Use of Small Animal Models for Duchenne and Parameters to Assess Efficiency upon Antisense Treatment
Ngoc Lu-Nguyen, Alberto Malerba, Linda Popplewell
F1000Research
|
September 6, 2016
Advances in gene therapy for muscular dystrophies
Hayder Abdul-Razak, Alberto Malerba, George Dickson
Human Gene Therapy
|
April 11, 2015
Progress on gene therapy, cell therapy, and pharmacological strategies toward the treatment of oculopharyngeal muscular dystrophy
Pradeep Harish, Alberto Malerba, George Dickson, et al.
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of 6
Search research articles
Search
Showing results (1-10 of 54) with videos related to
Sort By:
Page
of 6
Methods in Molecular Biology (Clifton, N.J.)
|
November 18, 2022
Systemic Delivery of a Monoclonal Antibody to Immunologically Block Myostatin in the A17 Mouse Model of OPMD
Alberto Malerba, Pradeep Harish, Linda Popplewell
Expert Opinion on Biological Therapy
|
May 22, 2018
The progress of AAV-mediated gene therapy in neuromuscular disorders
Sara Aguti, Alberto Malerba, Haiyan Zhou
Nucleic Acid Therapeutics
|
August 20, 2011
Long-term systemic administration of unconjugated morpholino oligomers for therapeutic expression of dystrophin by exon skipping in skeletal muscle: implications for cardiac muscle integrity
Alberto Malerba, Luisa Boldrin, George Dickson
Methods in Molecular Biology (Clifton, N.J.)
|
September 2, 2018
Systemic Intravenous Administration of Antisense Therapeutics for Combinatorial Dystrophin and Myostatin Exon Splice Modulation
Ngoc Lu-Nguyen, George Dickson, Alberto Malerba
Methods in Molecular Biology (Clifton, N.J.)
|
July 28, 2025
Systemic Intravenous Administration of Antisense Therapeutics for Combinatorial Dystrophin and Myostatin Exon Splice Modulation
Ngoc Lu-Nguyen, George Dickson, Alberto Malerba
Methods in Molecular Biology (Clifton, N.J.)
|
March 29, 2012
Optimizing antisense oligonucleotides using phosphorodiamidate morpholino oligomers
Linda J Popplewell, Alberto Malerba, George Dickson
Nucleic Acid Therapeutics
|
July 31, 2020
Researcher's Perceptions on Publishing "Negative" Results and Open Access
Lucía Echevarría, Alberto Malerba, Virginia Arechavala-Gomeza
Methods in Molecular Biology (Clifton, N.J.)
|
February 25, 2022
Use of Small Animal Models for Duchenne and Parameters to Assess Efficiency upon Antisense Treatment
Ngoc Lu-Nguyen, Alberto Malerba, Linda Popplewell
F1000Research
|
September 6, 2016
Advances in gene therapy for muscular dystrophies
Hayder Abdul-Razak, Alberto Malerba, George Dickson
Human Gene Therapy
|
April 11, 2015
Progress on gene therapy, cell therapy, and pharmacological strategies toward the treatment of oculopharyngeal muscular dystrophy
Pradeep Harish, Alberto Malerba, George Dickson, et al.
Page
of 6