These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 28546788)

  • 1.
    Niba ETE; Yamanaka R; Rani AQM; Awano H; Matsumoto M; Nishio H; Matsuo M
    Cancer Cell Int; 2017; 17():58. PubMed ID: 28546788
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular characterization of the 5'-UTR of retinal dystrophin reveals a cryptic intron that regulates translational activity.
    Kubokawa I; Takeshima Y; Ota M; Enomoto M; Okizuka Y; Mori T; Nishimura N; Awano H; Yagi M; Matsuo M
    Mol Vis; 2010 Dec; 16():2590-7. PubMed ID: 21151598
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Intronic Alternative Polyadenylation in the Middle of the
    Rani AQM; Yamamoto T; Kawaguchi T; Maeta K; Awano H; Nishio H; Matsuo M
    Int J Mol Sci; 2020 May; 21(10):. PubMed ID: 32443516
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Neuronal SH-SY5Y cells use the C-dystrophin promoter coupled with exon 78 skipping and display multiple patterns of alternative splicing including two intronic insertion events.
    Nishida A; Minegishi M; Takeuchi A; Awano H; Niba ET; Matsuo M
    Hum Genet; 2015 Sep; 134(9):993-1001. PubMed ID: 26152642
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Tissue- and case-specific retention of intron 40 in mature dystrophin mRNA.
    Nishida A; Minegishi M; Takeuchi A; Niba ET; Awano H; Lee T; Iijima K; Takeshima Y; Matsuo M
    J Hum Genet; 2015 Jun; 60(6):327-33. PubMed ID: 25833469
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel cryptic exon identified in the 3' region of intron 2 of the human dystrophin gene.
    Tran VK; Zhang Z; Yagi M; Nishiyama A; Habara Y; Takeshima Y; Matsuo M
    J Hum Genet; 2005; 50(8):425-433. PubMed ID: 16133659
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of a transcriptional enhancer within muscle intron 1 of the human dystrophin gene.
    Klamut HJ; Bosnoyan-Collins LO; Worton RG; Ray PN; Davis HL
    Hum Mol Genet; 1996 Oct; 5(10):1599-606. PubMed ID: 8894694
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of the shortest splice variant of Dp71, together with five known variants, in glioblastoma cells.
    Rani AQM; Farea M; Maeta K; Kawaguchi T; Awano H; Nagai M; Nishio H; Matsuo M
    Biochem Biophys Res Commun; 2019 Jan; 508(2):640-645. PubMed ID: 30527806
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.
    Den Dunnen JT; Grootscholten PM; Bakker E; Blonden LA; Ginjaar HB; Wapenaar MC; van Paassen HM; van Broeckhoven C; Pearson PL; van Ommen GJ
    Am J Hum Genet; 1989 Dec; 45(6):835-47. PubMed ID: 2573997
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Direct Reprogramming of Human DMD Fibroblasts into Myotubes for In Vitro Evaluation of Antisense-Mediated Exon Skipping and Exons 45-55 Skipping Accompanied by Rescue of Dystrophin Expression.
    Lee JJA; Saito T; Duddy W; Takeda S; Yokota T
    Methods Mol Biol; 2018; 1828():141-150. PubMed ID: 30171539
    [TBL] [Abstract][Full Text] [Related]  

  • 11. In Vitro Multiexon Skipping by Antisense PMOs in Dystrophic Dog and Exon 7-Deleted DMD Patient.
    Nakamura A; Aoki Y; Tsoumpra M; Yokota T; Takeda S
    Methods Mol Biol; 2018; 1828():151-163. PubMed ID: 30171540
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Exon 51 Skipping Quantification by Digital Droplet PCR in del52hDMD/mdx Mice.
    Hiller M; Spitali P; Datson N; Aartsma-Rus A
    Methods Mol Biol; 2018; 1828():249-262. PubMed ID: 30171546
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Schwann cell-specific Dp116 is expressed in glioblastoma cells, revealing two novel
    Mahyoob Rani AQ; Maeta K; Kawaguchi T; Awano H; Nagai M; Nishio H; Matsuo M
    Biochem Biophys Rep; 2019 Dec; 20():100703. PubMed ID: 31737793
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Modification of splicing in the dystrophin gene in cultured Mdx muscle cells by antisense oligoribonucleotides.
    Dunckley MG; Manoharan M; Villiet P; Eperon IC; Dickson G
    Hum Mol Genet; 1998 Jul; 7(7):1083-90. PubMed ID: 9618164
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A G-to-A transition at the fifth position of intron-32 of the dystrophin gene inactivates a splice-donor site both in vivo and in vitro.
    Thi Tran HT; Takeshima Y; Surono A; Yagi M; Wada H; Matsuo M
    Mol Genet Metab; 2005 Jul; 85(3):213-9. PubMed ID: 15979033
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Non-sequential and multi-step splicing of the dystrophin transcript.
    Gazzoli I; Pulyakhina I; Verwey NE; Ariyurek Y; Laros JF; 't Hoen PA; Aartsma-Rus A
    RNA Biol; 2016; 13(3):290-305. PubMed ID: 26670121
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.