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Molecular Therapy. Methods & Clinical Development|June 18, 2021
Functional recovery of a novel knockin mouse model of dysferlinopathy by readthrough of nonsense mutationKyowon Seo, Eun Kyoung Kim, Jaeil Choi, et al.Human Gene Therapy|October 5, 2011
A simplified immune suppression scheme leads to persistent micro-dystrophin expression in Duchenne muscular dystrophy dogsJin-Hong Shin, Yongping Yue, Arun Srivastava, et al.Journal of Molecular and Cellular Cardiology|May 17, 2012
AAV micro-dystrophin gene therapy alleviates stress-induced cardiac death but not myocardial fibrosis in >21-m-old mdx mice, an end-stage model of Duchenne muscular dystrophy cardiomyopathyBrian Bostick, Jin-Hong Shin, Yongping Yue, et al.Muscle & Nerve|November 13, 2015
NEB-related core-rod myopathy with distinct clinical and pathological featuresYoung-Eun Park, Jin-Hong Shin, Boram Kang, et al.Human Molecular Genetics|April 24, 2016
Genomic removal of a therapeutic mini-dystrophin gene from adult mice elicits a Duchenne muscular dystrophy-like phenotypeNalinda B Wasala, Yi Lai, Jin-Hong Shin, et al.Human Gene Therapy|February 14, 2018
Cardiac-Specific Expression of ΔH2-R15 Mini-Dystrophin Normalized All Electrocardiogram Abnormalities and the End-Diastolic Volume in a 23-Month-Old Mouse Model of Duchenne Dilated CardiomyopathyNalinda B Wasala, Jin-Hong Shin, Yi Lai, et al.Muscle & Nerve|April 19, 2018
Characterization of congenital myopathies at a Korean neuromuscular centerYoung-Eun Park, Jin-Hong Shin, Hyang-Sook Kim, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|October 23, 2008
Transduction efficiency and immune response associated with the administration of AAV8 vector into dog skeletal muscleSachiko Ohshima, Jin-Hong Shin, Katsutoshi Yuasa, et al.Scientific Reports|August 14, 2015
A start codon mutation of the FRMD7 gene in two Korean families with idiopathic infantile nystagmusJae-Hwan Choi, Jin-Hong Shin, Je Hyun Seo, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 13, 2014
Effect of enzyme replacement therapy in late onset Pompe disease: open pilot study of 48 weeks follow-upJin-Sung Park, Hye-Gyung Kim, Jin-Hong Shin, et al.Pageof 11