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 *

144 related articles for article (PubMed ID: 1307251)

  • 21. Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy.
    Muntoni F; Melis MA; Ganau A; Dubowitz V
    Am J Hum Genet; 1995 Jan; 56(1):151-7. PubMed ID: 7825571
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Apo-dystrophin-1 and apo-dystrophin-2, products of the Duchenne muscular dystrophy locus: expression during mouse embryogenesis and in cultured cell lines.
    Schofield JN; Blake DJ; Simmons C; Morris GE; Tinsley JM; Davies KE; Edwards YH
    Hum Mol Genet; 1994 Aug; 3(8):1309-16. PubMed ID: 7987307
    [TBL] [Abstract][Full Text] [Related]  

  • 23. New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin.
    Cox GA; Phelps SF; Chapman VM; Chamberlain JS
    Nat Genet; 1993 May; 4(1):87-93. PubMed ID: 8099842
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Modulation of in vitro splicing of the upstream intron by modifying an intra-exon sequence which is deleted from the dystrophin gene in dystrophin Kobe.
    Takeshima Y; Nishio H; Sakamoto H; Nakamura H; Matsuo M
    J Clin Invest; 1995 Feb; 95(2):515-20. PubMed ID: 7860733
    [TBL] [Abstract][Full Text] [Related]  

  • 25. G-utrophin, the autosomal homologue of dystrophin Dp116, is expressed in sensory ganglia and brain.
    Blake DJ; Schofield JN; Zuellig RA; Górecki DC; Phelps SR; Barnard EA; Edwards YH; Davies KE
    Proc Natl Acad Sci U S A; 1995 Apr; 92(9):3697-701. PubMed ID: 7731967
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A housekeeping type promoter, located in the 3' region of the Duchenne muscular dystrophy gene, controls the expression of Dp71, a major product of the gene.
    Lederfein D; Yaffe D; Nudel U
    Hum Mol Genet; 1993 Nov; 2(11):1883-8. PubMed ID: 8281151
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hybrid spectrin type repeats produced by exon-skipping in dystrophin.
    Menhart N
    Biochim Biophys Acta; 2006 Jun; 1764(6):993-9. PubMed ID: 16716778
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cells.
    Blake DJ; Love DR; Tinsley J; Morris GE; Turley H; Gatter K; Dickson G; Edwards YH; Davies KE
    Hum Mol Genet; 1992 May; 1(2):103-9. PubMed ID: 1301145
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Localization of dystrophin gene transcripts during mouse embryogenesis.
    Houzelstein D; Lyons GE; Chamberlain J; Buckingham ME
    J Cell Biol; 1992 Nov; 119(4):811-21. PubMed ID: 1429837
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Normal dystrophin transcripts detected in Duchenne muscular dystrophy patients after myoblast transplantation.
    Gussoni E; Pavlath GK; Lanctot AM; Sharma KR; Miller RG; Steinman L; Blau HM
    Nature; 1992 Apr; 356(6368):435-8. PubMed ID: 1557125
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Characterization and localization of a 77 kDa protein related to the dystrophin gene family.
    Fabbrizio E; Nudel U; Hugon G; Robert A; Pons F; Mornet D
    Biochem J; 1994 Apr; 299 ( Pt 2)(Pt 2):359-65. PubMed ID: 8172595
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Dystrophin muscle enhancer 1 is implicated in the activation of non-muscle isoforms in the skeletal muscle of patients with X-linked dilated cardiomyopathy.
    Bastianutto C; Bestard JA; Lahnakoski K; Broere D; De Visser M; Zaccolo M; Pozzan T; Ferlini A; Muntoni F; Patarnello T; Klamut HJ
    Hum Mol Genet; 2001 Nov; 10(23):2627-35. PubMed ID: 11726549
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Genomic organization of the mouse dystrobrevin gene: comparative analysis with the dystrophin gene.
    Ambrose HJ; Blake DJ; Nawrotzki RA; Davies KE
    Genomics; 1997 Feb; 39(3):359-69. PubMed ID: 9119373
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Expression of the transcripts initiated in the 62nd intron of the dystrophin gene.
    Lambert M; Chafey P; Hugnot JP; Koulakoff A; Berwald-Netter Y; Billard C; Morris GE; Kahn A; Kaplan JC; Gilgenkrantz H
    Neuromuscul Disord; 1993; 3(5-6):519-24. PubMed ID: 8186704
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. A second promoter provides an alternative target for therapeutic up-regulation of utrophin in Duchenne muscular dystrophy.
    Burton EA; Tinsley JM; Holzfeind PJ; Rodrigues NR; Davies KE
    Proc Natl Acad Sci U S A; 1999 Nov; 96(24):14025-30. PubMed ID: 10570192
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Correction of dystrophin expression in cells from Duchenne muscular dystrophy patients through genomic excision of exon 51 by zinc finger nucleases.
    Ousterout DG; Kabadi AM; Thakore PI; Perez-Pinera P; Brown MT; Majoros WH; Reddy TE; Gersbach CA
    Mol Ther; 2015 Mar; 23(3):523-32. PubMed ID: 25492562
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.