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 *

400 related articles for article (PubMed ID: 29800419)

  • 1. Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology.
    Bondue A; Arbustini E; Bianco A; Ciccarelli M; Dawson D; De Rosa M; Hamdani N; Hilfiker-Kleiner D; Meder B; Leite-Moreira AF; Thum T; Tocchetti CG; Varricchi G; Van der Velden J; Walsh R; Heymans S
    Cardiovasc Res; 2018 Aug; 114(10):1287-1303. PubMed ID: 29800419
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals.
    Kayvanpour E; Sedaghat-Hamedani F; Amr A; Lai A; Haas J; Holzer DB; Frese KS; Keller A; Jensen K; Katus HA; Meder B
    Clin Res Cardiol; 2017 Feb; 106(2):127-139. PubMed ID: 27576561
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dilated Cardiomyopathy: Genetic Determinants and Mechanisms.
    McNally EM; Mestroni L
    Circ Res; 2017 Sep; 121(7):731-748. PubMed ID: 28912180
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Metabolic changes in hypertrophic cardiomyopathies: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology.
    van der Velden J; Tocchetti CG; Varricchi G; Bianco A; Sequeira V; Hilfiker-Kleiner D; Hamdani N; Leite-Moreira AF; Mayr M; Falcão-Pires I; Thum T; Dawson DK; Balligand JL; Heymans S
    Cardiovasc Res; 2018 Aug; 114(10):1273-1280. PubMed ID: 29912308
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Subtle abnormalities in contractile function are an early manifestation of sarcomere mutations in dilated cardiomyopathy.
    Lakdawala NK; Thune JJ; Colan SD; Cirino AL; Farrohi F; Rivero J; McDonough B; Sparks E; Orav EJ; Seidman JG; Seidman CE; Ho CY
    Circ Cardiovasc Genet; 2012 Oct; 5(5):503-10. PubMed ID: 22949430
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dilated cardiomyopathy mutations in thin-filament regulatory proteins reduce contractility, suppress systolic Ca
    Robinson P; Sparrow AJ; Patel S; Malinowska M; Reilly SN; Zhang YH; Casadei B; Watkins H; Redwood C
    Am J Physiol Heart Circ Physiol; 2020 Aug; 319(2):H306-H319. PubMed ID: 32618513
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Advances in the Genetic Basis and Pathogenesis of Sarcomere Cardiomyopathies.
    Yotti R; Seidman CE; Seidman JG
    Annu Rev Genomics Hum Genet; 2019 Aug; 20():129-153. PubMed ID: 30978303
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.
    Kamisago M; Sharma SD; DePalma SR; Solomon S; Sharma P; McDonough B; Smoot L; Mullen MP; Woolf PK; Wigle ED; Seidman JG; Seidman CE
    N Engl J Med; 2000 Dec; 343(23):1688-96. PubMed ID: 11106718
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial dilated cardiomyopathy caused by an alpha-tropomyosin mutation: the distinctive natural history of sarcomeric dilated cardiomyopathy.
    Lakdawala NK; Dellefave L; Redwood CS; Sparks E; Cirino AL; Depalma S; Colan SD; Funke B; Zimmerman RS; Robinson P; Watkins H; Seidman CE; Seidman JG; McNally EM; Ho CY
    J Am Coll Cardiol; 2010 Jan; 55(4):320-9. PubMed ID: 20117437
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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;
    Clin Transl Sci; 2013 Dec; 6(6):424-8. PubMed ID: 24119082
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic mutations and mechanisms in dilated cardiomyopathy.
    McNally EM; Golbus JR; Puckelwartz MJ
    J Clin Invest; 2013 Jan; 123(1):19-26. PubMed ID: 23281406
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Functional abnormalities in induced Pluripotent Stem Cell-derived cardiomyocytes generated from titin-mutated patients with dilated cardiomyopathy.
    Schick R; Mekies LN; Shemer Y; Eisen B; Hallas T; Ben Jehuda R; Ben-Ari M; Szantai A; Willi L; Shulman R; Gramlich M; Pane LS; My I; Freimark D; Murgia M; Santamaria G; Gherghiceanu M; Arad M; Moretti A; Binah O
    PLoS One; 2018; 13(10):e0205719. PubMed ID: 30332462
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy.
    Jansweijer JA; Nieuwhof K; Russo F; Hoorntje ET; Jongbloed JD; Lekanne Deprez RH; Postma AV; Bronk M; van Rijsingen IA; de Haij S; Biagini E; van Haelst PL; van Wijngaarden J; van den Berg MP; Wilde AA; Mannens MM; de Boer RA; van Spaendonck-Zwarts KY; van Tintelen JP; Pinto YM
    Eur J Heart Fail; 2017 Apr; 19(4):512-521. PubMed ID: 27813223
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Modulating the tension-time integral of the cardiac twitch prevents dilated cardiomyopathy in murine hearts.
    Powers JD; Kooiker KB; Mason AB; Teitgen AE; Flint GV; Tardiff JC; Schwartz SD; McCulloch AD; Regnier M; Davis J; Moussavi-Harami F
    JCI Insight; 2020 Oct; 5(20):. PubMed ID: 32931484
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Sarcomeres and Cardiac Growth: Tension in the Relationship.
    Haldar SM; Srivastava D
    Trends Mol Med; 2016 Jul; 22(7):530-533. PubMed ID: 27237981
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity.
    Cattin ME; Bertrand AT; Schlossarek S; Le Bihan MC; Skov Jensen S; Neuber C; Crocini C; Maron S; Lainé J; Mougenot N; Varnous S; Fromes Y; Hansen A; Eschenhagen T; Decostre V; Carrier L; Bonne G
    Hum Mol Genet; 2013 Aug; 22(15):3152-64. PubMed ID: 23575224
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy.
    Forleo C; Carmosino M; Resta N; Rampazzo A; Valecce R; Sorrentino S; Iacoviello M; Pisani F; Procino G; Gerbino A; Scardapane A; Simone C; Calore M; Torretta S; Svelto M; Favale S
    PLoS One; 2015; 10(4):e0121723. PubMed ID: 25837155
    [TBL] [Abstract][Full Text] [Related]  

  • 19. How do mutations in contractile proteins cause the primary familial cardiomyopathies?
    Marston SB
    J Cardiovasc Transl Res; 2011 Jun; 4(3):245-55. PubMed ID: 21424860
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dilated cardiomyopathy caused by LMNA mutations. Clinical and morphological studies.
    Bilińska ZT; Sylvius N; Grzybowski J; Fidziańska A; Michalak E; Walczak E; Walski M; Bieganowska K; Szymaniak E; Kuśmierczyk-Droszcz B; Lubiszewska B; Wagner T; Tesson F; Ruzyłło W
    Kardiol Pol; 2006 Aug; 64(8):812-9; discussion 820-1. PubMed ID: 16981056
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.