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European Journal of Translational Myology
|
September 17, 2021
A revised model for mitochondrial dysfunction in Duchenne muscular dystrophy
Ai Vu Hong, Mathilde Sanson, Isabelle Richard, et al.
International Journal of Molecular Sciences
|
October 16, 2024
In Silico Structural Prediction for the Generation of Novel Performant Midi-Dystrophins Based on Intein-Mediated Dual AAV Approach
Laura Palmieri, Maxime Ferrand, Ai Vu Hong, et al.
Non-Coding RNA
|
July 27, 2022
Deciphering the Molecular Mechanism of Incurable Muscle Disease by a Novel Method for the Interpretation of miRNA Dysregulation
David Israeli, Ai Vu Hong, Guillaume Corre, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
May 26, 2021
Cholesterol metabolism is a potential therapeutic target in Duchenne muscular dystrophy
Fatima Amor, Ai Vu Hong, Guillaume Corre, et al.
Life Science Alliance
|
October 20, 2022
Dlk1-Dio3 cluster miRNAs regulate mitochondrial functions in the dystrophic muscle in Duchenne muscular dystrophy
Ai Vu Hong, Nathalie Bourg, Peggy Sanatine, et al.
Nature Communications
|
September 11, 2024
An engineered AAV targeting integrin alpha V beta 6 presents improved myotropism across species
Ai Vu Hong, Laurence Suel, Eva Petat, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 6, 2006
The INS VNTR locus does not associate with smallness for gestational age (SGA) but interacts with SGA to increase insulin resistance in young adults
Thuy-Ai Vu-Hong, Emmanuelle Durand, Samia Deghmoun, et al.
International Journal of Molecular Sciences
|
February 26, 2022
Co-Administration of Simvastatin Does Not Potentiate the Benefit of Gene Therapy in the mdx Mouse Model for Duchenne Muscular Dystrophy
Nathalie Bourg, Ai Vu Hong, William Lostal, et al.
NPJ Regenerative Medicine
|
April 14, 2026
Author Correction: Disease exacerbation in human DMD MYOrganoids enables gene therapy evaluation and unveils persistence of fibrotic activity
Laura Palmieri, Giorgia Bimbi, Maxime Ferrand, et al.
NPJ Regenerative Medicine
|
January 3, 2026
Disease exacerbation in human DMD MYOrganoids enables gene therapy evaluation and unveils persistence of fibrotic activity
Laura Palmieri, Giorgia Bimbi, Maxime Ferrand, et al.
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of 2
Search research articles
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Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
European Journal of Translational Myology
|
September 17, 2021
A revised model for mitochondrial dysfunction in Duchenne muscular dystrophy
Ai Vu Hong, Mathilde Sanson, Isabelle Richard, et al.
International Journal of Molecular Sciences
|
October 16, 2024
In Silico Structural Prediction for the Generation of Novel Performant Midi-Dystrophins Based on Intein-Mediated Dual AAV Approach
Laura Palmieri, Maxime Ferrand, Ai Vu Hong, et al.
Non-Coding RNA
|
July 27, 2022
Deciphering the Molecular Mechanism of Incurable Muscle Disease by a Novel Method for the Interpretation of miRNA Dysregulation
David Israeli, Ai Vu Hong, Guillaume Corre, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
May 26, 2021
Cholesterol metabolism is a potential therapeutic target in Duchenne muscular dystrophy
Fatima Amor, Ai Vu Hong, Guillaume Corre, et al.
Life Science Alliance
|
October 20, 2022
Dlk1-Dio3 cluster miRNAs regulate mitochondrial functions in the dystrophic muscle in Duchenne muscular dystrophy
Ai Vu Hong, Nathalie Bourg, Peggy Sanatine, et al.
Nature Communications
|
September 11, 2024
An engineered AAV targeting integrin alpha V beta 6 presents improved myotropism across species
Ai Vu Hong, Laurence Suel, Eva Petat, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 6, 2006
The INS VNTR locus does not associate with smallness for gestational age (SGA) but interacts with SGA to increase insulin resistance in young adults
Thuy-Ai Vu-Hong, Emmanuelle Durand, Samia Deghmoun, et al.
International Journal of Molecular Sciences
|
February 26, 2022
Co-Administration of Simvastatin Does Not Potentiate the Benefit of Gene Therapy in the mdx Mouse Model for Duchenne Muscular Dystrophy
Nathalie Bourg, Ai Vu Hong, William Lostal, et al.
NPJ Regenerative Medicine
|
April 14, 2026
Author Correction: Disease exacerbation in human DMD MYOrganoids enables gene therapy evaluation and unveils persistence of fibrotic activity
Laura Palmieri, Giorgia Bimbi, Maxime Ferrand, et al.
NPJ Regenerative Medicine
|
January 3, 2026
Disease exacerbation in human DMD MYOrganoids enables gene therapy evaluation and unveils persistence of fibrotic activity
Laura Palmieri, Giorgia Bimbi, Maxime Ferrand, et al.
Page
of 2