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Journal of Clinical Medicine
|
July 29, 2023
Limb-Girdle Muscular Dystrophies Classification and Therapies
Camille Bouchard, Jacques P Tremblay
Journal of Clinical Medicine
|
September 28, 2023
Portrait of Dysferlinopathy: Diagnosis and Development of Therapy
Camille Bouchard, Jacques P Tremblay
Medecine Sciences : M/S
|
October 25, 2024
[Correcting pathogenic mutations using prime editing: an overview]
Camille Bouchard, Kelly Godbout, Jacques P Tremblay
Genes & Diseases
|
January 26, 2026
Molecular characterization of a new R1925X point mutation mouse model for dysferlinopathy
Camille Bouchard, Louis Despax, Joël Rousseau, et al.
Behavioural Brain Research
|
September 11, 2022
A promising mouse model for Friedreich Ataxia progressing like human patients
Catherine Gérard, Annabelle Fortin Archambault, Camille Bouchard, et al.
Cells
|
May 27, 2026
Gene Editing Strategies for Duchenne Muscular Dystrophy: From Molecular Mechanisms to Clinical Translation
Ayesha Siddika, Joël Rousseau, Félix Veillette, et al.
International Journal of Molecular Sciences
|
June 26, 2025
In Vitro Correction of Point Mutations in the <i>DYSF</i> Gene Using Prime Editing
Camille Bouchard, Joël Rousseau, Gabriel Lamothe, et al.
Genes
|
August 26, 2023
Finding an Appropriate Mouse Model to Study the Impact of a Treatment for Friedreich Ataxia on the Behavioral Phenotype
Camille Bouchard, Catherine Gérard, Solange Gni-Fiene Yanyabé, et al.
Australasian Journal on Ageing
|
November 28, 2023
Factors influencing older adults' participation in telehealth interventions for primary prevention and health promotion: A rapid review
Samuel Turcotte, Camille Bouchard, Jacqueline Rousseau, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Journal of Clinical Medicine
|
July 29, 2023
Limb-Girdle Muscular Dystrophies Classification and Therapies
Camille Bouchard, Jacques P Tremblay
Journal of Clinical Medicine
|
September 28, 2023
Portrait of Dysferlinopathy: Diagnosis and Development of Therapy
Camille Bouchard, Jacques P Tremblay
Medecine Sciences : M/S
|
October 25, 2024
[Correcting pathogenic mutations using prime editing: an overview]
Camille Bouchard, Kelly Godbout, Jacques P Tremblay
Genes & Diseases
|
January 26, 2026
Molecular characterization of a new R1925X point mutation mouse model for dysferlinopathy
Camille Bouchard, Louis Despax, Joël Rousseau, et al.
Behavioural Brain Research
|
September 11, 2022
A promising mouse model for Friedreich Ataxia progressing like human patients
Catherine Gérard, Annabelle Fortin Archambault, Camille Bouchard, et al.
Cells
|
May 27, 2026
Gene Editing Strategies for Duchenne Muscular Dystrophy: From Molecular Mechanisms to Clinical Translation
Ayesha Siddika, Joël Rousseau, Félix Veillette, et al.
International Journal of Molecular Sciences
|
June 26, 2025
In Vitro Correction of Point Mutations in the <i>DYSF</i> Gene Using Prime Editing
Camille Bouchard, Joël Rousseau, Gabriel Lamothe, et al.
Genes
|
August 26, 2023
Finding an Appropriate Mouse Model to Study the Impact of a Treatment for Friedreich Ataxia on the Behavioral Phenotype
Camille Bouchard, Catherine Gérard, Solange Gni-Fiene Yanyabé, et al.
Australasian Journal on Ageing
|
November 28, 2023
Factors influencing older adults' participation in telehealth interventions for primary prevention and health promotion: A rapid review
Samuel Turcotte, Camille Bouchard, Jacqueline Rousseau, et al.
Page
of 1