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330 related items for PubMed ID: 10966831

  • 1. Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy.
    Olson TM, Doan TP, Kishimoto NY, Whitby FG, Ackerman MJ, Fananapazir L.
    J Mol Cell Cardiol; 2000 Sep; 32(9):1687-94. PubMed ID: 10966831
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  • 2. Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy.
    Nowak KJ, Wattanasirichaigoon D, Goebel HH, Wilce M, Pelin K, Donner K, Jacob RL, Hübner C, Oexle K, Anderson JR, Verity CM, North KN, Iannaccone ST, Müller CR, Nürnberg P, Muntoni F, Sewry C, Hughes I, Sutphen R, Lacson AG, Swoboda KJ, Vigneron J, Wallgren-Pettersson C, Beggs AH, Laing NG.
    Nat Genet; 1999 Oct; 23(2):208-12. PubMed ID: 10508519
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  • 5. Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy.
    Kabaeva ZT, Perrot A, Wolter B, Dietz R, Cardim N, Correia JM, Schulte HD, Aldashev AA, Mirrakhimov MM, Osterziel KJ.
    Eur J Hum Genet; 2002 Nov; 10(11):741-8. PubMed ID: 12404107
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  • 6. Hypertrophic cardiomyopathy in a Portuguese population: mutations in the myosin-binding protein C gene.
    Cardim N, Perrot A, Santos S, Morgado P, Pádua M, Ferreira S, Reis RP, Monteiro C, Ferreira T, Correia JM, Osterziel KJ.
    Rev Port Cardiol; 2005 Dec; 24(12):1463-76. PubMed ID: 16566405
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  • 8. Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy.
    Olson TM, Kishimoto NY, Whitby FG, Michels VV.
    J Mol Cell Cardiol; 2001 Apr; 33(4):723-32. PubMed ID: 11273725
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  • 9. Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects.
    Monserrat L, Hermida-Prieto M, Fernandez X, Rodríguez I, Dumont C, Cazón L, Cuesta MG, Gonzalez-Juanatey C, Peteiro J, Alvarez N, Penas-Lado M, Castro-Beiras A.
    Eur Heart J; 2007 Aug; 28(16):1953-61. PubMed ID: 17611253
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  • 11. Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy.
    Carniel E, Taylor MR, Sinagra G, Di Lenarda A, Ku L, Fain PR, Boucek MM, Cavanaugh J, Miocic S, Slavov D, Graw SL, Feiger J, Zhu XZ, Dao D, Ferguson DA, Bristow MR, Mestroni L.
    Circulation; 2005 Jul 05; 112(1):54-9. PubMed ID: 15998695
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  • 12. [Familial hypertrophic cardiomyopathy: genes, mutations and animal models. A review].
    Ramírez CD, Padrón R.
    Invest Clin; 2004 Mar 05; 45(1):69-99. PubMed ID: 15058760
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  • 14. Hypertrophic cardiomyopathy: an update.
    McKenna WJ.
    Cardiologia; 1993 Dec 05; 38(12 Suppl 1):277-81. PubMed ID: 8020027
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  • 15. Identification of a metavinculin missense mutation, R975W, associated with both hypertrophic and dilated cardiomyopathy.
    Vasile VC, Will ML, Ommen SR, Edwards WD, Olson TM, Ackerman MJ.
    Mol Genet Metab; 2006 Feb 05; 87(2):169-74. PubMed ID: 16236538
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  • 16. Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences.
    Doolan A, Tebo M, Ingles J, Nguyen L, Tsoutsman T, Lam L, Chiu C, Chung J, Weintraub RG, Semsarian C.
    J Mol Cell Cardiol; 2005 Feb 05; 38(2):387-93. PubMed ID: 15698845
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  • 17. A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy.
    Girolami F, Olivotto I, Passerini I, Zachara E, Nistri S, Re F, Fantini S, Baldini K, Torricelli F, Cecchi F.
    J Cardiovasc Med (Hagerstown); 2006 Aug 05; 7(8):601-7. PubMed ID: 16858239
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  • 18. Actin mutations in hypertrophic and dilated cardiomyopathy cause inefficient protein folding and perturbed filament formation.
    Vang S, Corydon TJ, Børglum AD, Scott MD, Frydman J, Mogensen J, Gregersen N, Bross P.
    FEBS J; 2005 Apr 05; 272(8):2037-49. PubMed ID: 15819894
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  • 19. Familial hypertrophic cardiomyopathy: a paradigm of the cardiac hypertrophic response to injury.
    Marian AJ, Roberts R.
    Ann Med; 1998 Aug 05; 30 Suppl 1():24-32. PubMed ID: 9800880
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  • 20. Prevalence of sarcomere protein gene mutations in preadolescent children with hypertrophic cardiomyopathy.
    Kaski JP, Syrris P, Esteban MT, Jenkins S, Pantazis A, Deanfield JE, McKenna WJ, Elliott PM.
    Circ Cardiovasc Genet; 2009 Oct 05; 2(5):436-41. PubMed ID: 20031618
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