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 *

156 related articles for article (PubMed ID: 12354438)

  • 1. 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]  

  • 2. 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]  

  • 3. Mutations in the dystrophin gene are associated with sporadic dilated cardiomyopathy.
    Feng J; Yan J; Buzin CH; Towbin JA; Sommer SS
    Mol Genet Metab; 2002; 77(1-2):119-26. PubMed ID: 12359139
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. A 5' dystrophin duplication mutation causes membrane deficiency of alpha-dystroglycan in a family with X-linked cardiomyopathy.
    Bies RD; Maeda M; Roberds SL; Holder E; Bohlmeyer T; Young JB; Campbell KP
    J Mol Cell Cardiol; 1997 Dec; 29(12):3175-88. PubMed ID: 9441825
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathy.
    Franz WM; Müller M; Müller OJ; Herrmann R; Rothmann T; Cremer M; Cohn RD; Voit T; Katus HA
    Lancet; 2000 May; 355(9217):1781-5. PubMed ID: 10832829
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Comprehensive scanning of the ATM gene with DOVAM-S.
    Buzin CH; Gatti RA; Nguyen VQ; Wen CY; Mitui M; Sanal O; Chen JS; Nozari G; Mengos A; Li X; Fujimura F; Sommer SS
    Hum Mutat; 2003 Feb; 21(2):123-31. PubMed ID: 12552559
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dilated cardiomyopathy and the dystrophin gene: an illustrated review.
    Oldfors A; Eriksson BO; Kyllerman M; Martinsson T; Wahlström J
    Br Heart J; 1994 Oct; 72(4):344-8. PubMed ID: 7833192
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [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]  

  • 15. A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathy.
    Ferlini A; Galié N; Merlini L; Sewry C; Branzi A; Muntoni F
    Am J Hum Genet; 1998 Aug; 63(2):436-46. PubMed ID: 9683584
    [TBL] [Abstract][Full Text] [Related]  

  • 16. X-linked dilated cardiomyopathy with a large hot-spot deletion in the dystrophin gene.
    Tasaki N; Yoshida K; Haruta SI; Kouno H; Ichinose H; Fujimoto Y; Urasawa N; Kawakami T; Taniguchi M; Kurushima S; Shimakura T
    Intern Med; 2001 Dec; 40(12):1215-21. PubMed ID: 11813847
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy.
    Cohen N; Muntoni F
    Heart; 2004 Aug; 90(8):835-41. PubMed ID: 15253946
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular basis of hypertrophic and dilated cardiomyopathy.
    Marian AJ; Roberts R
    Tex Heart Inst J; 1994; 21(1):6-15. PubMed ID: 8180512
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Study on mutations affecting the muscle promoter/first exon of the dystrophin gene in 92 Japanese dilated cardiomyopathy patients.
    Shiga N; Matsuo M; Yokoyama M; Yokota Y
    Am J Med Genet; 1998 Sep; 79(3):226-7. PubMed ID: 9788566
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.