Showing results (31-40 of 80) with videos related to

Sort By:
Pageof 8
Neurological Research|August 4, 2007
Increased ER stress during motor neuron degeneration in a transgenic mouse model of amyotrophic lateral sclerosisTetsuya Nagata, Hristelina Ilieva, Tetsuro Murakami, et al.
Molecular Therapy. Nucleic Acids|January 26, 2023
Change of intracellular calcium level causes acute neurotoxicity by antisense oligonucleotides via CSF routeChunyan Jia, Su Su Lei Mon, Ying Yang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 8, 2020
Efficient Gene Suppression by DNA/DNA Double-Stranded Oligonucleotide In VivoYutaro Asami, Tetsuya Nagata, Kotaro Yoshioka, et al.
Biochemical and Biophysical Research Communications|September 22, 2018
Truncated dystrophin ameliorates the dystrophic phenotype of mdx mice by reducing sarcolipin-mediated SERCA inhibitionJun Tanihata, Tetsuya Nagata, Naoki Ito, et al.
Nature|August 26, 2011
Three classical Cepheid variable stars in the nuclear bulge of the Milky WayNoriyuki Matsunaga, Takahiro Kawadu, Shogo Nishiyama, et al.
Science Translational Medicine|April 20, 2018
Systemic administration of the antisense oligonucleotide NS-065/NCNP-01 for skipping of exon 53 in patients with Duchenne muscular dystrophyHirofumi Komaki, Tetsuya Nagata, Takashi Saito, et al.
Bioorganic & Medicinal Chemistry Letters|December 16, 2018
Synthesis of 2'-O-(N-methylcarbamoylethyl) 5-methyl-2-thiouridine and its application to splice-switching oligonucleotidesYoshiaki Masaki, Keishi Yamamoto, Takeshi Inde, et al.
Plos One|July 30, 2013
Mutation types and aging differently affect revertant fiber expansion in dystrophic mdx and mdx52 miceYusuke Echigoya, Joshua Lee, Merryl Rodrigues, et al.
International Journal of Molecular Sciences|October 19, 2016
Endogenous Multiple Exon Skipping and Back-Splicing at the DMD Mutation HotspotHitoshi Suzuki, Yoshitsugu Aoki, Toshiki Kameyama, et al.
Pageof 8