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July 23, 2020
Current Status of Antisense Oligonucleotide-Based Therapy in Neuromuscular Disorders
Flavien Bizot, Adeline Vulin, Aurélie Goyenvalle
Drugs
|
August 5, 2020
Correction to: Current Status of Antisense Oligonucleotide-Based Therapy in Neuromuscular Disorders
Flavien Bizot, Adeline Vulin, Aurélie Goyenvalle
Mutation Research. Reviews in Mutation Research
|
December 7, 2016
Human epidermal stem cells: Role in adverse skin reactions and carcinogenesis from radiation
Michèle T Martin, Adeline Vulin, Jolyon H Hendry
Science (New York, N.Y.)
|
November 6, 2004
Rescue of dystrophic muscle through U7 snRNA-mediated exon skipping
Aurélie Goyenvalle, Adeline Vulin, Françoise Fougerousse, et al.
Medecine Sciences : M/S
|
December 8, 2004
[An opening in Duchenne muscular dystrophy: persistent therapeutic rescue of dystrophin by vectorized antisense mediated exon skipping in mdx mice]
Aurélie Goyenvalle, Adeline Vulin, Françoise Fougerousse, et al.
Molecular Therapy. Methods & Clinical Development
|
April 26, 2021
Pre-clinical dose-escalation studies establish a therapeutic range for U7snRNA-mediated <i>DMD</i> exon 2 skipping
Tabatha R Simmons, Tatyana A Vetter, Nianyuan Huang, et al.
Journal of Neuromuscular Diseases
|
September 5, 2017
Efficient Skipping of Single Exon Duplications in DMD Patient-Derived Cell Lines Using an Antisense Oligonucleotide Approach
Nicolas Wein, Adeline Vulin, Andrew R Findlay, et al.
Neuromuscular Disorders : NMD
|
September 15, 2015
The first exon duplication mouse model of Duchenne muscular dystrophy: A tool for therapeutic development
Adeline Vulin, Nicolas Wein, Tabatha R Simmons, et al.
Human Gene Therapy
|
April 11, 2009
Immortalized skin fibroblasts expressing conditional MyoD as a renewable and reliable source of converted human muscle cells to assess therapeutic strategies for muscular dystrophies: validation of an exon-skipping approach to restore dystrophin in Duchenne muscular dystrophy cells
Soraya Chaouch, Vincent Mouly, Aurélie Goyenvalle, et al.
International Journal of Radiation Oncology, Biology, Physics
|
September 8, 2018
Severe PATCHED1 Deficiency in Cancer-Prone Gorlin Patient Cells Results in Intrinsic Radiosensitivity
Adeline Vulin, Melissa Sedkaoui, Sandra Moratille, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
Drugs
|
July 23, 2020
Current Status of Antisense Oligonucleotide-Based Therapy in Neuromuscular Disorders
Flavien Bizot, Adeline Vulin, Aurélie Goyenvalle
Drugs
|
August 5, 2020
Correction to: Current Status of Antisense Oligonucleotide-Based Therapy in Neuromuscular Disorders
Flavien Bizot, Adeline Vulin, Aurélie Goyenvalle
Mutation Research. Reviews in Mutation Research
|
December 7, 2016
Human epidermal stem cells: Role in adverse skin reactions and carcinogenesis from radiation
Michèle T Martin, Adeline Vulin, Jolyon H Hendry
Science (New York, N.Y.)
|
November 6, 2004
Rescue of dystrophic muscle through U7 snRNA-mediated exon skipping
Aurélie Goyenvalle, Adeline Vulin, Françoise Fougerousse, et al.
Medecine Sciences : M/S
|
December 8, 2004
[An opening in Duchenne muscular dystrophy: persistent therapeutic rescue of dystrophin by vectorized antisense mediated exon skipping in mdx mice]
Aurélie Goyenvalle, Adeline Vulin, Françoise Fougerousse, et al.
Molecular Therapy. Methods & Clinical Development
|
April 26, 2021
Pre-clinical dose-escalation studies establish a therapeutic range for U7snRNA-mediated <i>DMD</i> exon 2 skipping
Tabatha R Simmons, Tatyana A Vetter, Nianyuan Huang, et al.
Journal of Neuromuscular Diseases
|
September 5, 2017
Efficient Skipping of Single Exon Duplications in DMD Patient-Derived Cell Lines Using an Antisense Oligonucleotide Approach
Nicolas Wein, Adeline Vulin, Andrew R Findlay, et al.
Neuromuscular Disorders : NMD
|
September 15, 2015
The first exon duplication mouse model of Duchenne muscular dystrophy: A tool for therapeutic development
Adeline Vulin, Nicolas Wein, Tabatha R Simmons, et al.
Human Gene Therapy
|
April 11, 2009
Immortalized skin fibroblasts expressing conditional MyoD as a renewable and reliable source of converted human muscle cells to assess therapeutic strategies for muscular dystrophies: validation of an exon-skipping approach to restore dystrophin in Duchenne muscular dystrophy cells
Soraya Chaouch, Vincent Mouly, Aurélie Goyenvalle, et al.
International Journal of Radiation Oncology, Biology, Physics
|
September 8, 2018
Severe PATCHED1 Deficiency in Cancer-Prone Gorlin Patient Cells Results in Intrinsic Radiosensitivity
Adeline Vulin, Melissa Sedkaoui, Sandra Moratille, et al.
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of 3