Tomoko Chiyo
Kodaira, 1878502, Japan
Last Updated: 09/26/2026
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Found 10 publications
Improved transduction of canine X-linked muscular dystrophy with rAAV9-microdystrophin via multipotent MSC pretreatment.
Journal: Molecular therapy. Methods & clinical development
Published: October 23, 2020
Supplemental Treatment for Huntington's Disease with miR-132 that Is Deficient in Huntington's Disease Brain.
Journal: Molecular therapy. Nucleic acids
Published: July 31, 2017
Fukutin is prerequisite to ameliorate muscular dystrophic phenotype by myofiber-selective LARGE expression.
Journal: Scientific reports
Published: October 08, 2014
Neuromuscular disease. DOK7 gene therapy benefits mouse models of diseases characterized by defects in the neuromuscular junction.
Journal: Science (New York, N.Y.)
Published: September 20, 2014
Dystrophic mdx mice develop severe cardiac and respiratory dysfunction following genetic ablation of the anti-inflammatory cytokine IL-10.
Journal: Human molecular genetics
Published: March 25, 2014
Intra-amniotic rAAV-mediated microdystrophin gene transfer improves canine X-linked muscular dystrophy and may induce immune tolerance.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: February 25, 2014
Specific inhibition of tumor cells by oncogenic EGFR specific silencing by RNA interference.
Journal: PloS one
Published: June 07, 2013
Robust Long-term Transduction of Common Marmoset Neuromuscular Tissue With rAAV1 and rAAV9.
Journal: Molecular therapy. Nucleic acids
Published: May 30, 2013
Impaired viability of muscle precursor cells in muscular dystrophy with glycosylation defects and amelioration of its severe phenotype by limited gene expression.
Journal: Human molecular genetics
Published: April 09, 2013
Immunization with a recombinant vaccinia virus that encodes nonstructural proteins of the hepatitis C virus suppresses viral protein levels in mouse liver.
Journal: PloS one
Published: March 13, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026