BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

510 related articles for article (PubMed ID: 27493940)

  • 1. A Review of the Giant Protein Titin in Clinical Molecular Diagnostics of Cardiomyopathies.
    Gigli M; Begay RL; Morea G; Graw SL; Sinagra G; Taylor MR; Granzier H; Mestroni L
    Front Cardiovasc Med; 2016; 3():21. PubMed ID: 27493940
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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;
    J Am Heart Assoc; 2015 Nov; 4(11):. PubMed ID: 26567375
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The Giant Protein Titin's Role in Cardiomyopathy: Genetic, Transcriptional, and Post-translational Modifications of TTN and Their Contribution to Cardiac Disease.
    Tharp CA; Haywood ME; Sbaizero O; Taylor MRG; Mestroni L
    Front Physiol; 2019; 10():1436. PubMed ID: 31849696
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A combinatorial oligogenic basis for the phenotypic plasticity between late-onset dilated and arrhythmogenic cardiomyopathy in a single family.
    Pourebrahim K; Marian JG; Tan Y; Chang JT; Marian AJ
    J Cardiovasc Aging; 2021; 1():. PubMed ID: 34790974
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic epidemiology of titin-truncating variants in the etiology of dilated cardiomyopathy.
    Tabish AM; Azzimato V; Alexiadis A; Buyandelger B; Knöll R
    Biophys Rev; 2017 Jun; 9(3):207-223. PubMed ID: 28510119
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 9(1):4093. PubMed ID: 30858397
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies.
    Waldmüller S; Schroeder C; Sturm M; Scheffold T; Imbrich K; Junker S; Frische C; Hofbeck M; Bauer P; Bonin M; Gawaz M; Gramlich M
    Mol Cell Probes; 2015 Oct; 29(5):308-14. PubMed ID: 25979592
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathy.
    Akinrinade O; Ollila L; Vattulainen S; Tallila J; Gentile M; Salmenperä P; Koillinen H; Kaartinen M; Nieminen MS; Myllykangas S; Alastalo TP; Koskenvuo JW; Heliö T
    Eur Heart J; 2015 Sep; 36(34):2327-37. PubMed ID: 26084686
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Truncations of titin causing dilated cardiomyopathy.
    Herman DS; Lam L; Taylor MR; Wang L; Teekakirikul P; Christodoulou D; Conner L; DePalma SR; McDonough B; Sparks E; Teodorescu DL; Cirino AL; Banner NR; Pennell DJ; Graw S; Merlo M; Di Lenarda A; Sinagra G; Bos JM; Ackerman MJ; Mitchell RN; Murry CE; Lakdawala NK; Ho CY; Barton PJ; Cook SA; Mestroni L; Seidman JG; Seidman CE
    N Engl J Med; 2012 Feb; 366(7):619-28. PubMed ID: 22335739
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Rapidly Evolving Role of Titin in Cardiac Physiology and Cardiomyopathy.
    Gerull B
    Can J Cardiol; 2015 Nov; 31(11):1351-9. PubMed ID: 26518445
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Titin mutations and muscle disease.
    Kellermayer D; Smith JE; Granzier H
    Pflugers Arch; 2019 May; 471(5):673-682. PubMed ID: 30919088
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 8(10):e1460. PubMed ID: 32815318
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies.
    Lu C; Wu W; Liu F; Yang K; Li J; Liu Y; Wang R; Si N; Gao P; Liu Y; Zhang S; Zhang X
    J Transl Med; 2018 Aug; 16(1):241. PubMed ID: 30165862
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Titin-truncating mutations associated with dilated cardiomyopathy alter length-dependent activation and its modulation via phosphorylation.
    Vikhorev PG; Vikhoreva NN; Yeung W; Li A; Lal S; Dos Remedios CG; Blair CA; Guglin M; Campbell KS; Yacoub MH; de Tombe P; Marston SB
    Cardiovasc Res; 2022 Jan; 118(1):241-253. PubMed ID: 33135063
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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;
    Circ Cardiovasc Genet; 2013 Apr; 6(2):144-53. PubMed ID: 23418287
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy.
    Gerull B; Gramlich M; Atherton J; McNabb M; Trombitás K; Sasse-Klaassen S; Seidman JG; Seidman C; Granzier H; Labeit S; Frenneaux M; Thierfelder L
    Nat Genet; 2002 Feb; 30(2):201-4. PubMed ID: 11788824
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Exploring TTN variants as genetic insights into cardiomyopathy pathogenesis and potential emerging clues to molecular mechanisms in cardiomyopathies.
    Jolfayi AG; Kohansal E; Ghasemi S; Naderi N; Hesami M; MozafaryBazargany M; Moghadam MH; Fazelifar AF; Maleki M; Kalayinia S
    Sci Rep; 2024 Mar; 14(1):5313. PubMed ID: 38438525
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy.
    van Spaendonck-Zwarts KY; Posafalvi A; van den Berg MP; Hilfiker-Kleiner D; Bollen IA; Sliwa K; Alders M; Almomani R; van Langen IM; van der Meer P; Sinke RJ; van der Velden J; Van Veldhuisen DJ; van Tintelen JP; Jongbloed JD
    Eur Heart J; 2014 Aug; 35(32):2165-73. PubMed ID: 24558114
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical Considerations for a Family with Dilated Cardiomyopathy, Sudden Cardiac Death, and a Novel
    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; 22(2):. PubMed ID: 33445410
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Next-Generation Sequencing Reveals Novel Genetic Variants for Dilated Cardiomyopathy in Pediatric Chinese Patients.
    Wang Y; Han B; Fan Y; Yi Y; Lv J; Wang J; Yang X; Jiang D; Zhao L; Zhang J; Yuan H
    Pediatr Cardiol; 2022 Jan; 43(1):110-120. PubMed ID: 34350506
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 26.