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 *

298 related articles for article (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;
    J Am Heart Assoc; 2015 Nov; 4(11):. PubMed ID: 26567375
    [TBL] [Abstract][Full Text] [Related]  

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

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

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

  • 5. Titin Truncating Variants in Dilated Cardiomyopathy - Prevalence and Genotype-Phenotype Correlations.
    Franaszczyk M; Chmielewski P; Truszkowska G; Stawinski P; Michalak E; Rydzanicz M; Sobieszczanska-Malek M; Pollak A; Szczygieł J; Kosinska J; Parulski A; Stoklosa T; Tarnowska A; Machnicki MM; Foss-Nieradko B; Szperl M; Sioma A; Kusmierczyk M; Grzybowski J; Zielinski T; Ploski R; Bilinska ZT
    PLoS One; 2017; 12(1):e0169007. PubMed ID: 28045975
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

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

  • 8. 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]  

  • 9. Low mutation rate in the TTN gene in paediatric patients with dilated cardiomyopathy - a pilot study.
    Zaklyazminskaya E; Mikhailov V; Bukaeva A; Kotlukova N; Povolotskaya I; Kaimonov V; Dombrovskaya A; Dzemeshkevich S
    Sci Rep; 2019 Nov; 9(1):16409. PubMed ID: 31712709
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

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

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

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

  • 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; 41(5):615-622. PubMed ID: 29750433
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy.
    Roncarati R; Viviani Anselmi C; Krawitz P; Lattanzi G; von Kodolitsch Y; Perrot A; di Pasquale E; Papa L; Portararo P; Columbaro M; Forni A; Faggian G; Condorelli G; Robinson PN
    Eur J Hum Genet; 2013 Oct; 21(10):1105-11. PubMed ID: 23463027
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 8(2):e1049. PubMed ID: 31880413
    [TBL] [Abstract][Full Text] [Related]  

  • 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;
    N Engl J Med; 2016 Jan; 374(3):233-41. PubMed ID: 26735901
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 62(2):359-366. PubMed ID: 33678800
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Reading Frame Repair of
    Romano R; Ghahremani S; Zimmerman T; Legere N; Thakar K; Ladha FA; Pettinato AM; Hinson JT
    Circulation; 2022 Jan; 145(3):194-205. PubMed ID: 34905694
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 15.