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 *

72 related articles for article (PubMed ID: 8476435)

  • 1. Expression of the dystrophin gene in cultured fibroblasts.
    Hugnot JP; Gilgenkrantz H; Chafey P; Lambert M; Eveno E; Kaplan JC; Kahn A
    Biochem Biophys Res Commun; 1993 Apr; 192(1):69-74. PubMed ID: 8476435
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Towards a therapeutic inhibition of dystrophin exon 23 splicing in mdx mouse muscle induced by antisense oligoribonucleotides (splicomers): target sequence optimisation using oligonucleotide arrays.
    Graham IR; Hill VJ; Manoharan M; Inamati GB; Dickson G
    J Gene Med; 2004 Oct; 6(10):1149-58. PubMed ID: 15386737
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients.
    Chelly J; Gilgenkrantz H; Hugnot JP; Hamard G; Lambert M; RĂ©can D; Akli S; Cometto M; Kahn A; Kaplan JC
    J Clin Invest; 1991 Oct; 88(4):1161-6. PubMed ID: 1918370
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of Becker muscular dystrophy resulting from the skipping of four contiguous exons (71-74) of the dystrophin gene during mRNA maturation.
    Patria SY; Alimsardjono H; Nishio H; Takeshima Y; Nakamura H; Matsuo M
    Proc Assoc Am Physicians; 1996 Jul; 108(4):308-14. PubMed ID: 8863344
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dystrophin gene transcribed from different promoters in neuronal and glial cells.
    Chelly J; Hamard G; Koulakoff A; Kaplan JC; Kahn A; Berwald-Netter Y
    Nature; 1990 Mar; 344(6261):64-5. PubMed ID: 2406613
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Expression of recombinant dystrophin and its localization to the cell membrane.
    Lee CC; Pearlman JA; Chamberlain JS; Caskey CT
    Nature; 1991 Jan; 349(6307):334-6. PubMed ID: 1824797
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus.
    Feener CA; Koenig M; Kunkel LM
    Nature; 1989 Apr; 338(6215):509-11. PubMed ID: 2648158
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Characterization of genetic deletions in Becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophin.
    Le Thiet Thanh ; Nguyen Thi Man ; Hori S; Sewry CA; Dubowitz V; Morris GE
    Am J Med Genet; 1995 Aug; 58(2):177-86. PubMed ID: 8533812
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Transcription of the dystrophin gene in human muscle and non-muscle tissue.
    Chelly J; Kaplan JC; Maire P; Gautron S; Kahn A
    Nature; 1988 Jun; 333(6176):858-60. PubMed ID: 3290682
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel cryptic exon in intron 2 of the human dystrophin gene evolved from an intron by acquiring consensus sequences for splicing at different stages of anthropoid evolution.
    Dwi Pramono ZA; Takeshima Y; Surono A; Ishida T; Matsuo M
    Biochem Biophys Res Commun; 2000 Jan; 267(1):321-8. PubMed ID: 10623618
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Six novel transcripts that remove a huge intron ranging from 250 to 800 kb are produced by alternative splicing of the 5' region of the dystrophin gene in human skeletal muscle.
    Surono A; Takeshima Y; Wibawa T; Pramono ZA; Matsuo M
    Biochem Biophys Res Commun; 1997 Oct; 239(3):895-9. PubMed ID: 9367866
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pseudoexon activation in the DMD gene as a novel mechanism for Becker muscular dystrophy.
    Tuffery-Giraud S; Saquet C; Chambert S; Claustres M
    Hum Mutat; 2003 Jun; 21(6):608-14. PubMed ID: 12754707
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A polymerase chain reaction screening strategy for the promoter of the canine dystrophin gene.
    Schatzberg S; Olby N; Steingold S; Keene B; Atkins C; Meurs K; Solomon G; Goedegebuure SA; Wilton S; Sharp N
    Am J Vet Res; 1999 Sep; 60(9):1040-6. PubMed ID: 10490068
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy.
    Shiga N; Takeshima Y; Sakamoto H; Inoue K; Yokota Y; Yokoyama M; Matsuo M
    J Clin Invest; 1997 Nov; 100(9):2204-10. PubMed ID: 9410897
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Therapy of Duchenne muscular dystrophy with umbilical cord blood stem cell transplantation].
    Zhang C; Feng HY; Huang SL; Fang JP; Xiao LL; Yao XL; Chen C; Ye X; Zeng Y; Lu XL; Wen JM; Zhang WX; Li Z; Feng SW; Xu HG; Huang K; Zhou DH; Chen W; Xie YM; Xi J; Zhang M; Li Y; Liu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):399-405. PubMed ID: 16086277
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The human dystrophin gene requires 16 hours to be transcribed and is cotranscriptionally spliced.
    Tennyson CN; Klamut HJ; Worton RG
    Nat Genet; 1995 Feb; 9(2):184-90. PubMed ID: 7719347
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Infidelity in the structure of ectopic transcripts: a novel exon in lymphocyte dystrophin transcripts.
    Roberts RG; Bentley DR; Bobrow M
    Hum Mutat; 1993; 2(4):293-9. PubMed ID: 8401537
    [TBL] [Abstract][Full Text] [Related]  

  • 18. DNA sequence analysis for structure/function and mutation studies in Becker muscular dystrophy.
    Hamed S; Sutherland-Smith A; Gorospe J; Kendrick-Jones J; Hoffman E
    Clin Genet; 2005 Jul; 68(1):69-79. PubMed ID: 15952989
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Point mutations in the dystrophin gene: evidence for frequent use of cryptic splice sites as a result of splicing defects.
    Tuffery-Giraud S; Chambert S; Demaille J; Claustres M
    Hum Mutat; 1999; 14(5):359-68. PubMed ID: 10533061
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Antisense oligonucleotide-induced exon skipping restores dystrophin expression in vitro in a canine model of DMD.
    McClorey G; Moulton HM; Iversen PL; Fletcher S; Wilton SD
    Gene Ther; 2006 Oct; 13(19):1373-81. PubMed ID: 16724091
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.