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 *

476 related articles for article (PubMed ID: 20215591)

  • 1. Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy.
    Hershberger RE; Norton N; Morales A; Li D; Siegfried JD; Gonzalez-Quintana J
    Circ Cardiovasc Genet; 2010 Apr; 3(2):155-61. PubMed ID: 20215591
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.
    Hershberger RE; Parks SB; Kushner JD; Li D; Ludwigsen S; Jakobs P; Nauman D; Burgess D; Partain J; Litt M
    Clin Transl Sci; 2008 May; 1(1):21-6. PubMed ID: 19412328
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives.
    Andersen PS; Havndrup O; Hougs L; Sørensen KM; Jensen M; Larsen LA; Hedley P; Thomsen AR; Moolman-Smook J; Christiansen M; Bundgaard H
    Hum Mutat; 2009 Mar; 30(3):363-70. PubMed ID: 19035361
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy.
    Carballo S; Robinson P; Otway R; Fatkin D; Jongbloed JD; de Jonge N; Blair E; van Tintelen JP; Redwood C; Watkins H
    Circ Res; 2009 Aug; 105(4):375-82. PubMed ID: 19590045
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [Mutations in genes for sarcomeric proteins].
    Kimura A
    Nihon Rinsho; 2000 Jan; 58(1):117-22. PubMed ID: 10885298
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM.
    Selvi Rani D; Nallari P; Dhandapany PS; Rani J; Meraj K; Ganesan M; Narasimhan C; Thangaraj K
    DNA Cell Biol; 2015 May; 34(5):350-9. PubMed ID: 25607779
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy.
    Núñez L; Gimeno-Blanes JR; Rodríguez-García MI; Monserrat L; Zorio E; Coats C; McGregor CG; Hernandez del Rincón JP; Castro-Beiras A; Hermida-Prieto M
    Circ J; 2013; 77(9):2358-65. PubMed ID: 23782526
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Familial hypertrophic cardiomyopathy: genes, mutations and animal models. A review].
    Ramírez CD; Padrón R
    Invest Clin; 2004 Mar; 45(1):69-99. PubMed ID: 15058760
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy.
    Kärkkäinen S; Heliö T; Jääskeläinen P; Miettinen R; Tuomainen P; Ylitalo K; Kaartinen M; Reissell E; Toivonen L; Nieminen MS; Kuusisto J; Laakso M; Peuhkurinen K
    Eur J Heart Fail; 2004 Dec; 6(7):861-8. PubMed ID: 15556047
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Meta-analysis of cardiomyopathy-associated variants in troponin genes identifies loci and intragenic hot spots that are associated with worse clinical outcomes.
    Tadros HJ; Life CS; Garcia G; Pirozzi E; Jones EG; Datta S; Parvatiyar MS; Chase PB; Allen HD; Kim JJ; Pinto JR; Landstrom AP
    J Mol Cell Cardiol; 2020 May; 142():118-125. PubMed ID: 32278834
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects.
    Posch MG; Waldmuller S; Müller M; Scheffold T; Fournier D; Andrade-Navarro MA; De Geeter B; Guillaumont S; Dauphin C; Yousseff D; Schmitt KR; Perrot A; Berger F; Hetzer R; Bouvagnet P; Özcelik C
    PLoS One; 2011; 6(12):e28872. PubMed ID: 22194935
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Clinical features, spectrum of causal genetic mutations and outcome of hypertrophic cardiomyopathy in South Africans.
    Ntusi NA; Shaboodien G; Badri M; Gumedze F; Mayosi BM
    Cardiovasc J Afr; 2016; 27(3):152-158. PubMed ID: 27841901
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel mutations in beta-myosin heavy chain, actin and troponin-I genes associated with dilated cardiomyopathy in Indian population.
    Boda U; Vadapalli S; Calambur N; Nallari P
    J Genet; 2009 Dec; 88(3):373-7. PubMed ID: 20086309
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy.
    Mori AA; Castro LR; Bortolin RH; Bastos GM; Oliveira VF; Ferreira GM; Hirata TDC; Fajardo CM; Sampaio MF; Moreira DAR; Pachón-Mateos JC; Correia EB; Sousa AGMR; Brión M; Carracedo A; Hirata RDC; Hirata MH
    Forensic Sci Int Genet; 2021 May; 52():102478. PubMed ID: 33588347
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 24.