Ji-su Lee
Seoul, Republic of Korea
Last Updated: 09/26/2026
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Found 8 publications
Targeted PMP22 TATA-box editing by CRISPR/Cas9 reduces demyelinating neuropathy of Charcot-Marie-Tooth disease type 1A in mice.
Journal: Nucleic acids research
Published: May 05, 2019
miR-381 Attenuates Peripheral Neuropathic Phenotype Caused by Overexpression of PMP22.
Journal: Experimental neurobiology
Published: January 23, 2019
Aminosalicylic acid reduces ER stress and Schwann cell death induced by MPZ mutations.
Journal: International journal of molecular medicine
Published: December 14, 2018
Clinical characterization and genetic analysis of Korean patients with X-linked Charcot-Marie-Tooth disease type 1.
Journal: Journal of the peripheral nervous system : JPNS
Published: December 15, 2016
Pmp22 mutant allele-specific siRNA alleviates demyelinating neuropathic phenotype in vivo.
Journal: Neurobiology of disease
Published: June 10, 2016
ADSSL1 mutation relevant to autosomal recessive adolescent onset distal myopathy.
Journal: Annals of neurology
Published: June 08, 2015
Overexpression of mutant HSP27 causes axonal neuropathy in mice.
Journal: Journal of biomedical science
Published: March 02, 2015
A novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathy.
Journal: BMC neurology
Published: December 15, 2014
Showing 1-8 of 8
Last Updated: 09/26/2026