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Dwi U. Kemaladewi
Dwi U. Kemaladewi
University of Toronto
Biology
Genetics
CRISPR
Exon
Duchenne muscular dystrophy
11
Papers
255
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A mutation-independent approach via transcriptional upregulation of a disease modifier gene rescues muscular dystrophy in vivo.
2018
bioRxiv
Dwi U. Kemaladewi
Prabhpreet S Bassi
Kyle Lindsay
Steven Erwood
Elzbieta Hyatt
Kara M Place
Ryan Marks
Kinga I. Gawlik
Madeleine Durbeej
Evgueni A. Ivakine
Ronald D. Cohn
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Citations (2)
CRISPR/Cas9-mediated exon inclusion in Lama2 gene alleviates dystrophic pathology in MDC1A mouse model
2016
Neuromuscular Disorders
Dwi U. Kemaladewi
E. Hyatt
Zhenya Ivakine
Ronald D. Cohn
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Spell Checking Nature: A Therapeutic Use of the CRISPR/Cas9 System in Duchenne Muscular Dystrophy
2015
Daria Wojtal
Dwi U. Kemaladewi
Zeenat Malam
Sarah Abdullah
E. Hyatt
Huang
Mouly
Thomas Voit
Francesco Muntoni
Evgueni A. Ivakine
Ronald D. Cohn
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