Concepedia

Author

Aurélie Goyenvalle

InsermORCID

Also Known As

A Goyenvalle, A. Goyenvalle, Aurelie Goyenvalle, Aurelie T Goyenvalle, Aurélie Goyenvalle, Aurélie Goyenvalle, Aurélie Goyenvalle, David Gilot, Goyenvalle, A., Goyenvalle, Aurélie

125

Publications

3.7K

Citations

29

H-Index

52

Concepts

All Affiliations

InsermCentre National de la Recherche ScientifiqueUniversité de Versailles Saint-Quentin-en-YvelinesUniversité Paris-SaclayUniversity of Oxford
AG

About

Aurélie Goyenvalle is an author at Inserm specializing in medicine, cell biology, and systems biology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

10

10

1.4K

2

Engineering

4

4

392

3

Natural Sciences

3

3

881

4

Health Sciences

1

1

27

5

Applied Physiology

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1

27

Aurélie Goyenvalle

×

40

Publications

2.5K

Citations

25

H-Index

YearCitations

Rescue of Dystrophic Muscle Through U7 snRNA-Mediated Exon Skipping

Aurélie Goyenvalle, Adeline Vulin, Françoise Fougerousse,

Science

2004

474

Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomers

Aurélie Goyenvalle, Graziella Griffith, Arran Babbs,

Nature Medicine

2015

306

Restoration of Human Dystrophin Following Transplantation of Exon-Skipping-Engineered DMD Patient Stem Cells into Dystrophic Mice

Rachid Benchaouir, Mirella Meregalli, Andrea Farini,

Cell stem cell

2007

223

Muscle Function Recovery in Golden Retriever Muscular Dystrophy After AAV1-U7 Exon Skipping

Adeline Vulin, Inès Barthélémy, Aurélie Goyenvalle,

Molecular Therapy

2012

128

Prevention of Dystrophic Pathology in Severely Affected Dystrophin/Utrophin-deficient Mice by Morpholino-oligomer-mediated Exon-skipping

Aurélie Goyenvalle, Arran Babbs, D. Powell,

Molecular Therapy

2009

102

Rescue of severely affected dystrophin/utrophin-deficient mice through scAAV-U7snRNA-mediated exon skipping

Aurélie Goyenvalle, Arran Babbs, J. Claire Wright,

Human Molecular Genetics

2012

101

Self-Assembly into Nanoparticles Is Essential for Receptor Mediated Uptake of Therapeutic Antisense Oligonucleotides

Kariem Ezzat, Yoshitsugu Aoki, Taeyoung Koo,

Nano Letters

2015

96

Enhanced Exon-skipping Induced by U7 snRNA Carrying a Splicing Silencer Sequence: Promising Tool for DMD Therapy

Aurélie Goyenvalle, Arran Babbs, Gert‐Jan B. van Ommen,

Molecular Therapy

2009

79

Efficacy and Safety Profile of Tricyclo-DNA Antisense Oligonucleotides in Duchenne Muscular Dystrophy Mouse Model

Karima Relizani, Graziella Griffith, Lucía Echevarría,

Molecular Therapy — Nucleic Acids

2017

73

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,

Human Gene Therapy

2009

71

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