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5. Contributions of Japanese patients to development of antisense therapy for DMD. Matsuo M; Takeshima Y; Nishio H Brain Dev; 2016 Jan; 38(1):4-9. PubMed ID: 26094594 [TBL] [Abstract][Full Text] [Related]
6. Skipping multiple exons of dystrophin transcripts using cocktail antisense oligonucleotides. Echigoya Y; Yokota T Nucleic Acid Ther; 2014 Feb; 24(1):57-68. PubMed ID: 24380394 [TBL] [Abstract][Full Text] [Related]
7. Exon skipping therapy for Duchenne muscular dystrophy. Kole R; Krieg AM Adv Drug Deliv Rev; 2015 Jun; 87():104-7. PubMed ID: 25980936 [TBL] [Abstract][Full Text] [Related]
8. Intravenous infusion of an antisense oligonucleotide results in exon skipping in muscle dystrophin mRNA of Duchenne muscular dystrophy. Takeshima Y; Yagi M; Wada H; Ishibashi K; Nishiyama A; Kakumoto M; Sakaeda T; Saura R; Okumura K; Matsuo M Pediatr Res; 2006 May; 59(5):690-4. PubMed ID: 16627883 [TBL] [Abstract][Full Text] [Related]
9. Rescue of dystrophin mRNA of Duchenne muscular dystrophy by inducing exon skipping. Matsuo M; Takeshima Y Acta Myol; 2005 Oct; 24(2):110-4. PubMed ID: 16550927 [TBL] [Abstract][Full Text] [Related]
10. A novel approach to identify Duchenne muscular dystrophy patients for aminoglycoside antibiotics therapy. Kimura S; Ito K; Miyagi T; Hiranuma T; Yoshioka K; Ozasa S; Matsukura M; Ikezawa M; Matsuo M; Takeshima Y; Miike T Brain Dev; 2005 Sep; 27(6):400-5. PubMed ID: 16122626 [TBL] [Abstract][Full Text] [Related]
11. Systemic administration of the antisense oligonucleotide NS-065/NCNP-01 for skipping of exon 53 in patients with Duchenne muscular dystrophy. Komaki H; Nagata T; Saito T; Masuda S; Takeshita E; Sasaki M; Tachimori H; Nakamura H; Aoki Y; Takeda S Sci Transl Med; 2018 Apr; 10(437):. PubMed ID: 29669851 [TBL] [Abstract][Full Text] [Related]
12. [Treatment of Duchenne muscular dystrophy with gentamicin]. Matsuo M; Takeshima Y; Yagi M; Ishibashi K; Wada H No To Hattatsu; 2004 Mar; 36(2):125-9. PubMed ID: 15031986 [TBL] [Abstract][Full Text] [Related]
18. Exon skipping for nonsense mutations in Duchenne muscular dystrophy: too many mutations, too few patients? Yokota T; Duddy W; Echigoya Y; Kolski H Expert Opin Biol Ther; 2012 Sep; 12(9):1141-52. PubMed ID: 22650324 [TBL] [Abstract][Full Text] [Related]
19. Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy. Béroud C; Tuffery-Giraud S; Matsuo M; Hamroun D; Humbertclaude V; Monnier N; Moizard MP; Voelckel MA; Calemard LM; Boisseau P; Blayau M; Philippe C; Cossée M; Pagès M; Rivier F; Danos O; Garcia L; Claustres M Hum Mutat; 2007 Feb; 28(2):196-202. PubMed ID: 17041910 [TBL] [Abstract][Full Text] [Related]
20. Chimeric RNA/ethylene-bridged nucleic acids promote dystrophin expression in myocytes of duchenne muscular dystrophy by inducing skipping of the nonsense mutation-encoding exon. Surono A; Van Khanh T; Takeshima Y; Wada H; Yagi M; Takagi M; Koizumi M; Matsuo M Hum Gene Ther; 2004 Aug; 15(8):749-57. PubMed ID: 15319032 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]