Dominique L. Ouellet

发表

Identification of functional microRNAs released through asymmetrical processing of HIV-1 TAR element†

Louis Flamand, M. Tremblay, I. Plante, 2008, Nucleic acids research.

MicroRNAs in Gene Regulation: When the Smallest Governs It All

P. Provost, Patrick Provost, D. Ouellet, 2006, Journal of biomedicine & biotechnology.

Nucleolar Localization of HIV-1 Rev Is Required, Yet Insufficient for Production of Infectious Viral Particles

J. Burnett, J. Rossi, Haitang Li, 2018, AIDS research and human retroviruses.

Increased Frataxin Expression Induced in Friedreich Ataxia Cells by Platinum TALE-VP64s or Platinum TALE-SunTag

J. Rousseau, C. Gérard, P. Chapdelaine, 2018, Molecular therapy. Nucleic acids.

Dicer-Derived MicroRNAs Are Utilized by the Fragile X Mental Retardation Protein for Assembly on Target RNAs

É. Khandjian, L. Davidovic, S. Tremblay, 2006, Journal of biomedicine & biotechnology.

Regulatory RNAs: future perspectives in diagnosis, prognosis, and individualized therapy.

P. Provost, Vincent Boissonneault, D. Ouellet, 2007, Methods in molecular biology.

Regulation of host gene expression by HIV-1 TAR microRNAs

J. Burnett, J. Rossi, I. Plante, 2013, Retrovirology.

RNAi and small interfering RNAs in human disease therapeutic applications.

John J Rossi, J. Rossi, M. Lares, 2010, Trends in biotechnology.

Existence of a microRNA pathway in anucleate platelets

G. Rousseau, I. Plante, P. Provost, 2009, Nature Structural &Molecular Biology.

Efficient Restoration of the Dystrophin Gene Reading Frame and Protein Structure in DMD Myoblasts Using the CinDel Method

J. Rousseau, P. Lagüe, P. Chapdelaine, 2016, Molecular therapy. Nucleic acids.

CRISPR-induced deletion with SaCas9 restores dystrophin expression in dystrophic models in vitro and in vivo

J. Rousseau, D. Ouellet, Dominique L. Ouellet, 2018, bioRxiv.

Gene Editing for Duchenne Muscular Dystrophy Using the CRISPR/Cas9 Technology: The Importance of Fine-tuning the Approach.

D. Ouellet, Dominique L. Ouellet, J. Tremblay, 2016, Molecular therapy : the journal of the American Society of Gene Therapy.

From gRNA Identification to the Restoration of Dystrophin Expression: A Dystrophin Gene Correction Strategy for Duchenne Muscular Dystrophy Mutations Using the CRISPR-Induced Deletion Method.

J. Rousseau, D. Ouellet, Dominique L. Ouellet, 2018, Methods in molecular biology.

Advances and challenges of using CRISPR-Cas9 gene editing for treating Duchenne muscular dystrophy

D. Ouellet, Dominique L. Ouellet, J. Tremblay, 2017 .

Corrigendum to “Efficient Restoration of the Dystrophin Gene Reading Frame and Protein Structure in DMD Myoblasts Using the CinDel Method”

J. Rousseau, P. Lagüe, P. Chapdelaine, 2016, Molecular therapy. Nucleic acids.

Human Dicer C-terminus functions as a 5-lipoxygenase binding domain.

I. Plante, B. Samuelsson, O. Rådmark, 2009, Biochimica et biophysica acta.