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Journal Abstract Search

299 related items for PubMed ID: 26567375

  • 1. Role of Titin Missense Variants in Dilated Cardiomyopathy.
    Begay RL, Graw S, Sinagra G, Merlo M, Slavov D, Gowan K, Jones KL, Barbati G, Spezzacatene A, Brun F, Di Lenarda A, Smith JE, Granzier HL, Mestroni L, Taylor M, Familial Cardiomyopathy Registry.
    J Am Heart Assoc; 2015 Nov 13; 4(11):. PubMed ID: 26567375
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  • 2. Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy.
    Akinrinade O, Heliö T, Lekanne Deprez RH, Jongbloed JDH, Boven LG, van den Berg MP, Pinto YM, Alastalo TP, Myllykangas S, Spaendonck-Zwarts KV, van Tintelen JP, van der Zwaag PA, Koskenvuo J.
    Sci Rep; 2019 Mar 11; 9(1):4093. PubMed ID: 30858397
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  • 3. A mutation in the glutamate-rich region of RNA-binding motif protein 20 causes dilated cardiomyopathy through missplicing of titin and impaired Frank-Starling mechanism.
    Beqqali A, Bollen IA, Rasmussen TB, van den Hoogenhof MM, van Deutekom HW, Schafer S, Haas J, Meder B, Sørensen KE, van Oort RJ, Mogensen J, Hubner N, Creemers EE, van der Velden J, Pinto YM.
    Cardiovasc Res; 2016 Oct 11; 112(1):452-63. PubMed ID: 27496873
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  • 4. Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.
    Merlo M, Sinagra G, Carniel E, Slavov D, Zhu X, Barbati G, Spezzacatene A, Ramani F, Salcedo E, Di Lenarda A, Mestroni L, Taylor MR, Familial Cardiomyopathy Registry.
    Clin Transl Sci; 2013 Dec 11; 6(6):424-8. PubMed ID: 24119082
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  • 6. Clinical Considerations for a Family with Dilated Cardiomyopathy, Sudden Cardiac Death, and a Novel TTN Frameshift Mutation.
    Micaglio E, Monasky MM, Bernardini A, Mecarocci V, Borrelli V, Ciconte G, Locati ET, Piccoli M, Ghiroldi A, Anastasia L, Pappone C.
    Int J Mol Sci; 2021 Jan 12; 22(2):. PubMed ID: 33445410
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  • 7. Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy.
    Norton N, Li D, Rampersaud E, Morales A, Martin ER, Zuchner S, Guo S, Gonzalez M, Hedges DJ, Robertson PD, Krumm N, Nickerson DA, Hershberger RE, National Heart, Lung, and Blood Institute GO Exome Sequencing Project and the Exome Sequencing Project Family Studies Project Team.
    Circ Cardiovasc Genet; 2013 Apr 12; 6(2):144-53. PubMed ID: 23418287
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  • 11. Whole-Exome Sequencing Identifies Two Novel TTN Mutations in Chinese Families with Dilated Cardiomyopathy.
    Liu JS, Fan LL, Zhang H, Liu X, Huang H, Tao LJ, Xia K, Xiang R.
    Cardiology; 2017 Apr 12; 136(1):10-14. PubMed ID: 27544385
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  • 13. Novel heterozygous truncating titin variants affecting the A-band are associated with cardiomyopathy and myopathy/muscular dystrophy.
    Rich KA, Moscarello T, Siskind C, Brock G, Tan CA, Vatta M, Winder TL, Elsheikh B, Vicini L, Tucker B, Palettas M, Hershberger RE, Kissel JT, Morales A, Roggenbuck J.
    Mol Genet Genomic Med; 2020 Oct 12; 8(10):e1460. PubMed ID: 32815318
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  • 14. Absence of a primary role for TTN missense variants in arrhythmogenic cardiomyopathy: From a clinical and pathological perspective.
    Chen K, Song J, Wang Z, Rao M, Chen L, Hu S.
    Clin Cardiol; 2018 May 12; 41(5):615-622. PubMed ID: 29750433
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  • 16. Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers.
    Verdonschot JAJ, Robinson EL, James KN, Mohamed MW, Claes GRF, Casas K, Vanhoutte EK, Hazebroek MR, Kringlen G, Pasierb MM, van den Wijngaard A, Glatz JFC, Heymans SRB, Krapels IPC, Nahas S, Brunner HG, Szklarczyk R.
    Mol Genet Genomic Med; 2020 Feb 12; 8(2):e1049. PubMed ID: 31880413
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  • 17. Shared Genetic Predisposition in Peripartum and Dilated Cardiomyopathies.
    Ware JS, Li J, Mazaika E, Yasso CM, DeSouza T, Cappola TP, Tsai EJ, Hilfiker-Kleiner D, Kamiya CA, Mazzarotto F, Cook SA, Halder I, Prasad SK, Pisarcik J, Hanley-Yanez K, Alharethi R, Damp J, Hsich E, Elkayam U, Sheppard R, Kealey A, Alexis J, Ramani G, Safirstein J, Boehmer J, Pauly DF, Wittstein IS, Thohan V, Zucker MJ, Liu P, Gorcsan J, McNamara DM, Seidman CE, Seidman JG, Arany Z, IMAC-2 and IPAC Investigators.
    N Engl J Med; 2016 Jan 21; 374(3):233-41. PubMed ID: 26735901
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