Tatianna Y. Wong
Toronto, ON M5G0A4, Canada
Last Updated: 09/26/2026
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Found 8 publications
Generation and characterization of a mouse model of Becker muscular dystrophy with a deletion of Dmd exons 52 to 55.
Journal: Disease models & mechanisms
Published: November 17, 2023
Prevention of early-onset cardiomyopathy in Dmd exon 52-54 deletion mice by CRISPR-Cas9-mediated exon skipping.
Journal: Molecular therapy. Methods & clinical development
Published: April 20, 2023
Targeted genome editing in vivo corrects a Dmd duplication restoring wild-type dystrophin expression.
Journal: EMBO molecular medicine
Published: August 04, 2020
A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic Dmd deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathy.
Journal: Disease models & mechanisms
Published: April 24, 2020
Therapeutic Applications of CRISPR/Cas for Duchenne Muscular Dystrophy.
Journal: Current gene therapy
Published: June 24, 2017
Pellicle formation in the malaria parasite.
Journal: Journal of cell science
Published: October 01, 2015
Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited Disorders.
Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited Disorders.
Journal: American journal of human genetics
Published: August 04, 2015
The role of palmitoylation for protein recruitment to the inner membrane complex of the malaria parasite.
Journal: The Journal of biological chemistry
Published: November 27, 2014
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Last Updated: 09/26/2026