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 *

139 related articles for article (PubMed ID: 11726549)

  • 1. 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]  

  • 2. The mouse dystrophin muscle enhancer-1 imparts skeletal muscle, but not cardiac muscle, expression onto the dystrophin Purkinje promoter in transgenic mice.
    De Repentigny Y; Marshall P; Worton RG; Kothary R
    Hum Mol Genet; 2004 Nov; 13(22):2853-62. PubMed ID: 15385445
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel muscle-specific enhancer identified within the deletion overlap region of two XLDC patients lacking muscle exon 1 of the human dystrophin gene.
    Bastianutto C; De Visser M; Muntoni F; Klamut HJ; Patarnello T
    Genomics; 2002 Dec; 80(6):614-20. PubMed ID: 12504853
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A point mutation in the 5' splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy.
    Milasin J; Muntoni F; Severini GM; Bartoloni L; Vatta M; Krajinovic M; Mateddu A; Angelini C; Camerini F; Falaschi A; Mestroni L; Giacca M
    Hum Mol Genet; 1996 Jan; 5(1):73-9. PubMed ID: 8789442
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. The absence of dystrophin brain isoform expression in healthy human heart ventricles explains the pathogenesis of 5' X-linked dilated cardiomyopathy.
    Neri M; Valli E; Alfano G; Bovolenta M; Spitali P; Rapezzi C; Muntoni F; Banfi S; Perini G; Gualandi F; Ferlini A
    BMC Med Genet; 2012 Mar; 13():20. PubMed ID: 22455600
    [TBL] [Abstract][Full Text] [Related]  

  • 7. X-linked dilated cardiomyopathy and the dystrophin gene.
    Ferlini A; Sewry C; Melis MA; Mateddu A; Muntoni F
    Neuromuscul Disord; 1999 Jul; 9(5):339-46. PubMed ID: 10407857
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart.
    Muntoni F; Wilson L; Marrosu G; Marrosu MG; Cianchetti C; Mestroni L; Ganau A; Dubowitz V; Sewry C
    J Clin Invest; 1995 Aug; 96(2):693-9. PubMed ID: 7635962
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy.
    Muntoni F; Di Lenarda A; Porcu M; Sinagra G; Mateddu A; Marrosu G; Ferlini A; Cau M; Milasin J; Melis MA; Marrosu MG; Cianchetti C; Sanna A; Falaschi A; Camerini F; Giacca M; Mestroni L
    Heart; 1997 Dec; 78(6):608-12. PubMed ID: 9470882
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Comprehensive mutation scanning of the dystrophin gene in patients with nonsyndromic X-linked dilated cardiomyopathy.
    Feng J; Yan JY; Buzin CH; Sommer SS; Towbin JA
    J Am Coll Cardiol; 2002 Sep; 40(6):1120-4. PubMed ID: 12354438
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A muscle-specific enhancer within intron 1 of the human dystrophin gene is functionally dependent on single MEF-1/E box and MEF-2/AT-rich sequence motifs.
    Klamut HJ; Bosnoyan-Collins LO; Worton RG; Ray PN
    Nucleic Acids Res; 1997 Apr; 25(8):1618-25. PubMed ID: 9092671
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel mutation in splicing donor of dystrophin gene first exon in a patient with dilated cardiomyopathy but no clinical signs of skeletal myopathy.
    Kimura S; Ikezawa M; Ozasa S; Ito K; Ueno H; Yoshioka K; Ijiri S; Nomura K; Nakamura K; Matuskura M; Miike T
    J Child Neurol; 2007 Jul; 22(7):901-6. PubMed ID: 17715288
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Mutations of the dystrophin gene in dilated cardiomyopathy].
    Shiga N; Akita H; Yokoyama M
    Nihon Rinsho; 2000 Jan; 58(1):123-7. PubMed ID: 10885299
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the human.
    Neri M; Torelli S; Brown S; Ugo I; Sabatelli P; Merlini L; Spitali P; Rimessi P; Gualandi F; Sewry C; Ferlini A; Muntoni F
    Neuromuscul Disord; 2007 Dec; 17(11-12):913-8. PubMed ID: 17826093
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy.
    Ortiz-Lopez R; Li H; Su J; Goytia V; Towbin JA
    Circulation; 1997 May; 95(10):2434-40. PubMed ID: 9170407
    [TBL] [Abstract][Full Text] [Related]  

  • 18. X-linked dilated cardiomyopathy. Novel mutation of the dystrophin gene.
    Franz WM; Cremer M; Herrmann R; Grünig E; Fogel W; Scheffold T; Goebel HH; Kircheisen R; Kübler W; Voit T
    Ann N Y Acad Sci; 1995 Mar; 752():470-91. PubMed ID: 7755293
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutation.
    Rimessi P; Gualandi F; Duprez L; Spitali P; Neri M; Merlini L; Calzolari E; Muntoni F; Ferlini A
    Am J Med Genet A; 2005 Feb; 132A(4):391-4. PubMed ID: 15641026
    [TBL] [Abstract][Full Text] [Related]  

  • 20. X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.
    Towbin JA; Hejtmancik JF; Brink P; Gelb B; Zhu XM; Chamberlain JS; McCabe ER; Swift M
    Circulation; 1993 Jun; 87(6):1854-65. PubMed ID: 8504498
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.