BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

341 related articles for article (PubMed ID: 32969603)

  • 1. Genomic study of dilated cardiomyopathy in a group of Mexican patients using site-directed next generation sequencing.
    Carnevale A; Rosas-Madrigal S; Rosendo-Gutiérrez R; López-Mora E; Romero-Hidalgo S; Avila-Vazzini N; Jacobo-Albavera L; Domínguez-Pérez M; Vargas-Alarcón G; Pérez-Villatoro F; Navarrete-Martínez JI; Villarreal-Molina MT
    Mol Genet Genomic Med; 2020 Nov; 8(11):e1504. PubMed ID: 32969603
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic basis of cardiomyopathy and the genotypes involved in prognosis and left ventricular reverse remodeling.
    Tobita T; Nomura S; Fujita T; Morita H; Asano Y; Onoue K; Ito M; Imai Y; Suzuki A; Ko T; Satoh M; Fujita K; Naito AT; Furutani Y; Toko H; Harada M; Amiya E; Hatano M; Takimoto E; Shiga T; Nakanishi T; Sakata Y; Ono M; Saito Y; Takashima S; Hagiwara N; Aburatani H; Komuro I
    Sci Rep; 2018 Jan; 8(1):1998. PubMed ID: 29386531
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Digenic Inheritance of LAMA4 and MYH7 Mutations in Patient with Infantile Dilated Cardiomyopathy.
    Abdallah AM; Carlus SJ; Al-Mazroea AH; Alluqmani M; Almohammadi Y; Bhuiyan ZA; Al-Harbi KM
    Medicina (Kaunas); 2019 Jan; 55(1):. PubMed ID: 30650640
    [No Abstract]   [Full Text] [Related]  

  • 4. The genetics of dilated cardiomyopathy: a prioritized candidate gene study of LMNA, TNNT2, TCAP, and PLN.
    Hirtle-Lewis M; Desbiens K; Ruel I; Rudzicz N; Genest J; Engert JC; Giannetti N
    Clin Cardiol; 2013 Oct; 36(10):628-33. PubMed ID: 24037902
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy.
    Millat G; Bouvagnet P; Chevalier P; Sebbag L; Dulac A; Dauphin C; Jouk PS; Delrue MA; Thambo JB; Le Metayer P; Seronde MF; Faivre L; Eicher JC; Rousson R
    Eur J Med Genet; 2011; 54(6):e570-5. PubMed ID: 21846512
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy.
    Petropoulou E; Soltani M; Firoozabadi AD; Namayandeh SM; Crockford J; Maroofian R; Jamshidi Y
    Eur J Med Genet; 2017 Sep; 60(9):485-488. PubMed ID: 28642161
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system.
    Zhao Y; Cao H; Song Y; Feng Y; Ding X; Pang M; Zhang Y; Zhang H; Ding J; Xia X
    Int J Mol Med; 2016 Jun; 37(6):1511-20. PubMed ID: 27082122
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Molecular characterization of Portuguese patients with dilated cardiomyopathy.
    Sousa A; Canedo P; Azevedo O; Lopes L; Pinho T; Baixia M; Rocha-Gonçalves F; Gonçalves L; Cardoso JS; Machado JC; Martins E;
    Rev Port Cardiol (Engl Ed); 2019 Feb; 38(2):129-139. PubMed ID: 30871747
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Targeted next-generation sequencing of candidate genes reveals novel mutations in patients with dilated cardiomyopathy.
    Zhao Y; Feng Y; Zhang YM; Ding XX; Song YZ; Zhang AM; Liu L; Zhang H; Ding JH; Xia XS
    Int J Mol Med; 2015 Dec; 36(6):1479-86. PubMed ID: 26458567
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic Basis and Genotype-Phenotype Correlations in Han Chinese Patients with Idiopathic Dilated Cardiomyopathy.
    Zhang XL; Xie J; Lan RF; Kang LN; Wang L; Xu W; Xu B
    Sci Rep; 2020 Feb; 10(1):2226. PubMed ID: 32041989
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic analysis using targeted next-generation sequencing of sporadic Chinese patients with idiopathic dilated cardiomyopathy.
    Li M; Xia S; Xu L; Tan H; Yang J; Wu Z; He X; Li L
    J Transl Med; 2021 May; 19(1):189. PubMed ID: 33941202
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic variants identified by target next-generation sequencing in heart transplant patients with dilated cardiomyopathy.
    Martins E; Sousa A; Canedo P; Leite S; Pinto R; Campelo M; Amorim S; Moura B; Lopes JM; Machado JC; Silva Cardoso J;
    Rev Port Cardiol (Engl Ed); 2019 Jun; 38(6):441-447. PubMed ID: 31303467
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 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. Targeted Next-Generation Sequencing Reveals Hot Spots and Doubly Heterozygous Mutations in Chinese Patients with Familial Cardiomyopathy.
    Zhao Y; Feng Y; Zhang YM; Ding XX; Song YZ; Zhang AM; Liu L; Zhang H; Ding JH; Xia XS
    Biomed Res Int; 2015; 2015():561819. PubMed ID: 26199943
    [TBL] [Abstract][Full Text] [Related]  

  • 17. DSP p.(Thr2104Glnfs*12) variant presents variably with early onset severe arrhythmias and left ventricular cardiomyopathy.
    Heliö K; Kangas-Kontio T; Weckström S; Vanninen SUM; Aalto-Setälä K; Alastalo TP; Myllykangas S; Heliö TM; Koskenvuo JW
    BMC Med Genet; 2020 Jan; 21(1):19. PubMed ID: 32005173
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Nonsense mutations in BAG3 are associated with early-onset dilated cardiomyopathy in French Canadians.
    Chami N; Tadros R; Lemarbre F; Lo KS; Beaudoin M; Robb L; Labuda D; Tardif JC; Racine N; Talajic M; Lettre G
    Can J Cardiol; 2014 Dec; 30(12):1655-61. PubMed ID: 25448463
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 18.