Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sayaka Mayama"'
Autor:
Shohko Sekine, Sayaka Mayama, Nobuaki Nishijima, Takuo Kojima, Yoko Endo-Takahashi, Yuko Ishii, Hitomi Shiono, Saki Akiyama, Akane Sakurai, Sanae Sashida, Nobuhito Hamano, Rui Tada, Ryo Suzuki, Kazuo Maruyama, Yoichi Negishi
Publikováno v:
Pharmaceutics, Vol 15, Iss 6, p 1665 (2023)
Strategies for gene and nucleic acid delivery to skeletal muscles have been extensively explored to treat Duchenne muscular dystrophy (DMD) and other neuromuscular diseases. Of these, effective intravascular delivery of naked plasmid DNA (pDNA) and n
Externí odkaz:
https://doaj.org/article/f46d1c15875344d78c0899d9609a3248
Autor:
Negishi, Shohko Sekine, Sayaka Mayama, Nobuaki Nishijima, Takuo Kojima, Yoko Endo-Takahashi, Yuko Ishii, Hitomi Shiono, Saki Akiyama, Akane Sakurai, Sanae Sashida, Nobuhito Hamano, Rui Tada, Ryo Suzuki, Kazuo Maruyama, Yoichi
Publikováno v:
Pharmaceutics; Volume 15; Issue 6; Pages: 1665
Strategies for gene and nucleic acid delivery to skeletal muscles have been extensively explored to treat Duchenne muscular dystrophy (DMD) and other neuromuscular diseases. Of these, effective intravascular delivery of naked plasmid DNA (pDNA) and n
Autor:
Shoko Sekine, Yoko Endo-Takahashi, Takuo Kojima, Yuko Ishii, Taiki Kikuchi, Nobuhito Hamano, Yoichi Negishi, Ryo Suzuki, Yukihiko Aramaki, Saki Akiyama, Sayaka Mayama, Kazuo Maruyama, Hitomi Shiono
Publikováno v:
Molecular Pharmaceutics. 11:1053-1061
Duchenne muscular dystrophy (DMD) is a genetic disorder that is caused by mutations in the DMD gene that lead to an absence of functional protein. The mdx dystrophic mouse contains a nonsense mutation in exon 23 of the dystrophin gene; a phosphorodia