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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

330 related items for PubMed ID: 29109008

  • 1. The pathogenic gene screening in a Chinese familial dilated cardiomyopathy pedigree from Hubei.
    Lyu Y, Chen J, Xu H.
    Gene; 2018 Feb 05; 642():159-162. PubMed ID: 29109008
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. 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 05; 112(1):452-63. PubMed ID: 27496873
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. 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 Oct 05; 136(1):10-14. PubMed ID: 27544385
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. 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 21; 35(32):2165-73. PubMed ID: 24558114
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Whole-exome sequencing reveals doubly novel heterozygous Myosin Binding Protein C and Titin mutations in a Chinese patient with severe dilated cardiomyopathy.
    Fan LL, Chen YQ, Huang H, Jin JY, Li JJ, Tan ZP.
    Cardiol Young; 2018 Dec 21; 28(12):1410-1414. PubMed ID: 30109841
    [Abstract] [Full Text] [Related]

  • 13. 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 07; 118(1):241-253. PubMed ID: 33135063
    [Abstract] [Full Text] [Related]

  • 14. The assembly and evaluation of antisense oligonucleotides applied in exon skipping for titin-based mutations in dilated cardiomyopathy.
    Hahn JK, Neupane B, Pradhan K, Zhou Q, Testa L, Pelzl L, Maleck C, Gawaz M, Gramlich M.
    J Mol Cell Cardiol; 2019 Jun 07; 131():12-19. PubMed ID: 30998980
    [Abstract] [Full Text] [Related]

  • 15. A Novel Titin Truncation Variant Linked to Familial Dilated Cardiomyopathy Found in a Japanese Family and Its Functional Analysis in Genome-Edited Model Cells.
    Hirayama-Yamada K, Inagaki N, Hayashi T, Kimura A.
    Int Heart J; 2021 Mar 30; 62(2):359-366. PubMed ID: 33678800
    [Abstract] [Full Text] [Related]

  • 16. Titin mutation in familial restrictive cardiomyopathy.
    Peled Y, Gramlich M, Yoskovitz G, Feinberg MS, Afek A, Polak-Charcon S, Pras E, Sela BA, Konen E, Weissbrod O, Geiger D, Gordon PM, Thierfelder L, Freimark D, Gerull B, Arad M.
    Int J Cardiol; 2014 Jan 15; 171(1):24-30. PubMed ID: 24315344
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. A missense variant in the titin gene in Doberman pinscher dogs with familial dilated cardiomyopathy and sudden cardiac death.
    Meurs KM, Friedenberg SG, Kolb J, Saripalli C, Tonino P, Woodruff K, Olby NJ, Keene BW, Adin DB, Yost OL, DeFrancesco TC, Lahmers S, Tou S, Shelton GD, Granzier H.
    Hum Genet; 2019 May 15; 138(5):515-524. PubMed ID: 30715562
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. 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 21; 6(2):144-53. PubMed ID: 23418287
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 17.