Showing results (11-20 of 80) with videos related to
Sort By:
Pageof 8
Organic & Biomolecular Chemistry|September 19, 2017
Synthesis and thermal stabilities of oligonucleotides containing 2'-O,4'-C-methylene bridged nucleic acid with a phenoxazine baseYuki Kishimoto, Akane Fujii, Osamu Nakagawa, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|September 9, 2010
In-frame dystrophin following exon 51-skipping improves muscle pathology and function in the exon 52-deficient mdx mouseYoshitsugu Aoki, Akinori Nakamura, Toshifumi Yokota, et al.Brain Research|October 15, 2003
Hypoxic induction of vascular endothelial growth factor is selectively impaired in mice carrying the mutant SOD1 geneTetsuro Murakami, Hristelina Ilieva, Mito Shiote, et al.Nature Communications|December 22, 2025
Morpholino-RNA duplex exhibits robust, sustained, and safe steric-block antisense activity by intracerebroventricular and intrathecal injectionMitsugu Yanagidaira, Tetsuya Nagata, Juri Hasegawa, et al.Diabetes|March 11, 2022
The Role of Long Noncoding RNA MALAT1 in Diabetic Polyneuropathy and the Impact of Its Silencing in the Dorsal Root Ganglion by a DNA/RNA Heteroduplex OligonucleotideAkiko Miyashita, Masaki Kobayashi, Satoru Ishibashi, et al.Journal of Neuroscience Research|October 20, 2005
Prevention of spinal motor neuron death by insulin-like growth factor-1 associating with the signal transduction systems in SODG93A transgenic miceHisashi Narai, Isao Nagano, Hristeina Ilieva, et al.Human Molecular Genetics|July 25, 2013
Highly efficient in vivo delivery of PMO into regenerating myotubes and rescue in laminin-α2 chain-null congenital muscular dystrophy miceYoshitsugu Aoki, Tetsuya Nagata, Toshifumi Yokota, et al.Muscle & Nerve|August 24, 2005
Late-onset distal myopathy with rimmed vacuoles without mutation in the GNE or dysferlin genesNaoki Suzuki, Masashi Aoki, Hideki Mizuno, et al.Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|January 14, 2005
Deficiency of PAR-2 gene increases acute focal ischemic brain injuryGuang Jin, Takeshi Hayashi, Junichi Kawagoe, et al.The Tohoku Journal of Experimental Medicine|August 6, 2005
Unique cerebellar-cerebral form of autosomal recessive ataxiaEtsuro Matsubara, Tetsuya Nagata, Yasuhiko Kageyama, et al.Pageof 8