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44. By-passing the nonsense mutation in the 4 CV mouse model of muscular dystrophy by induced exon skipping. Mitrpant C; Fletcher S; Iversen PL; Wilton SD J Gene Med; 2009 Jan; 11(1):46-56. PubMed ID: 19006096 [TBL] [Abstract][Full Text] [Related]
45. 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]
46. Splicing analysis disclosed a determinant single nucleotide for exon skipping caused by a novel intraexonic four-nucleotide deletion in the dystrophin gene. Tran VK; Takeshima Y; Zhang Z; Yagi M; Nishiyama A; Habara Y; Matsuo M J Med Genet; 2006 Dec; 43(12):924-30. PubMed ID: 16738009 [TBL] [Abstract][Full Text] [Related]
47. Exonic sequences provide better targets for antisense oligonucleotides than splice site sequences in the modulation of Duchenne muscular dystrophy splicing. Aartsma-Rus A; Houlleberghs H; van Deutekom JC; van Ommen GJ; 't Hoen PA Oligonucleotides; 2010 Apr; 20(2):69-77. PubMed ID: 20377429 [TBL] [Abstract][Full Text] [Related]
48. Categorization of 77 dystrophin exons into 5 groups by a decision tree using indexes of splicing regulatory factors as decision markers. Malueka RG; Takaoka Y; Yagi M; Awano H; Lee T; Dwianingsih EK; Nishida A; Takeshima Y; Matsuo M BMC Genet; 2012 Mar; 13():23. PubMed ID: 22462762 [TBL] [Abstract][Full Text] [Related]
53. Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy kobe. Matsuo M; Masumura T; Nishio H; Nakajima T; Kitoh Y; Takumi T; Koga J; Nakamura H J Clin Invest; 1991 Jun; 87(6):2127-31. PubMed ID: 2040695 [TBL] [Abstract][Full Text] [Related]
54. Modification of pre-mRNA processing: application to dystrophin expression. Wilton SD; Fletcher S Curr Opin Mol Ther; 2006 Apr; 8(2):130-5. PubMed ID: 16610765 [TBL] [Abstract][Full Text] [Related]
55. Endogenous Multiple Exon Skipping and Back-Splicing at the DMD Mutation Hotspot. Suzuki H; Aoki Y; Kameyama T; Saito T; Masuda S; Tanihata J; Nagata T; Mayeda A; Takeda S; Tsukahara T Int J Mol Sci; 2016 Oct; 17(10):. PubMed ID: 27754374 [TBL] [Abstract][Full Text] [Related]
56. Local dystrophin restoration with antisense oligonucleotide PRO051. van Deutekom JC; Janson AA; Ginjaar IB; Frankhuizen WS; Aartsma-Rus A; Bremmer-Bout M; den Dunnen JT; Koop K; van der Kooi AJ; Goemans NM; de Kimpe SJ; Ekhart PF; Venneker EH; Platenburg GJ; Verschuuren JJ; van Ommen GJ N Engl J Med; 2007 Dec; 357(26):2677-86. PubMed ID: 18160687 [TBL] [Abstract][Full Text] [Related]
57. Quantitative Evaluation of Exon Skipping in Immortalized Muscle Cells In Vitro. Lim KRQ; Yokota T Methods Mol Biol; 2018; 1828():127-139. PubMed ID: 30171538 [TBL] [Abstract][Full Text] [Related]
58. In vitro splicing analysis showed that availability of a cryptic splice site is not a determinant for alternative splicing patterns caused by +1G-->A mutations in introns of the dystrophin gene. Habara Y; Takeshima Y; Awano H; Okizuka Y; Zhang Z; Saiki K; Yagi M; Matsuo M J Med Genet; 2009 Aug; 46(8):542-7. PubMed ID: 19001018 [TBL] [Abstract][Full Text] [Related]
59. Comparative analysis of antisense oligonucleotide analogs for targeted DMD exon 46 skipping in muscle cells. Aartsma-Rus A; Kaman WE; Bremmer-Bout M; Janson AA; den Dunnen JT; van Ommen GJ; van Deutekom JC Gene Ther; 2004 Sep; 11(18):1391-8. PubMed ID: 15229633 [TBL] [Abstract][Full Text] [Related]
60. Chemical treatment enhances skipping of a mutated exon in the dystrophin gene. Nishida A; Kataoka N; Takeshima Y; Yagi M; Awano H; Ota M; Itoh K; Hagiwara M; Matsuo M Nat Commun; 2011; 2():308. PubMed ID: 21556062 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]