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146 related items for PubMed ID: 27350668

  • 1. Role of common sarcomeric gene polymorphisms in genetic susceptibility to left ventricular dysfunction.
    Kumar S, Mishra A, Srivastava A, Bhatt M, Garg N, Agarwal SK, Pande S, Mittal B.
    J Genet; 2016 Jun; 95(2):263-72. PubMed ID: 27350668
    [Abstract] [Full Text] [Related]

  • 2. Association of 25 bp deletion in MYBPC3 gene with left ventricle dysfunction in coronary artery disease patients.
    Srivastava A, Garg N, Mittal T, Khanna R, Gupta S, Seth PK, Mittal B.
    PLoS One; 2011 Jun; 6(9):e24123. PubMed ID: 21915287
    [Abstract] [Full Text] [Related]

  • 3. Role of inflammatory gene polymorphisms in left ventricular dysfunction (LVD) susceptibility in coronary artery disease (CAD) patients.
    Mishra A, Srivastava A, Mittal T, Garg N, Mittal B.
    Cytokine; 2013 Mar; 61(3):856-61. PubMed ID: 23357300
    [Abstract] [Full Text] [Related]

  • 4. Association of natriuretic peptide polymorphisms with left ventricular dysfunction in southern Han Chinese coronary artery disease patients.
    Wu Z, Xu M, Sheng H, Lou Y, Su X, Chen Y, Lu L, Liu Y, Jin W.
    Int J Clin Exp Pathol; 2014 Mar; 7(10):7148-57. PubMed ID: 25400811
    [Abstract] [Full Text] [Related]

  • 5. Role of angiotensin II type I (AT1 A1166C) receptor polymorphism in susceptibility of left ventricular dysfunction.
    Mishra A, Srivastava A, Kumar S, Mittal T, Garg N, Agarwal SK, Pande S, Mittal B.
    Indian Heart J; 2015 Mar; 67(3):214-21. PubMed ID: 26138177
    [Abstract] [Full Text] [Related]

  • 6. Association of matrix metalloproteinases (MMP2, MMP7 and MMP9) genetic variants with left ventricular dysfunction in coronary artery disease patients.
    Mishra A, Srivastava A, Mittal T, Garg N, Mittal B.
    Clin Chim Acta; 2012 Oct 09; 413(19-20):1668-74. PubMed ID: 22664146
    [Abstract] [Full Text] [Related]

  • 7. Impact of renin-angiotensin-aldosterone system gene polymorphisms on left ventricular dysfunction in coronary artery disease patients.
    Mishra A, Srivastava A, Mittal T, Garg N, Mittal B.
    Dis Markers; 2012 Oct 09; 32(1):33-41. PubMed ID: 22297600
    [Abstract] [Full Text] [Related]

  • 8. Genetic predisposition to left ventricular dysfunction: a multigenic and multi-analytical approach.
    Mishra A, Srivastava A, Mittal T, Garg N, Mittal B.
    Gene; 2014 Aug 10; 546(2):309-17. PubMed ID: 24875414
    [Abstract] [Full Text] [Related]

  • 9. Sarcomeric Gene Variants and Their Role with Left Ventricular Dysfunction in Background of Coronary Artery Disease.
    Kumar S, Kumar V, Kim JJ.
    Biomolecules; 2020 Mar 12; 10(3):. PubMed ID: 32178433
    [Abstract] [Full Text] [Related]

  • 10. Detection of a large duplication mutation in the myosin-binding protein C3 gene in a case of hypertrophic cardiomyopathy.
    Meyer T, Pankuweit S, Richter A, Maisch B, Ruppert V.
    Gene; 2013 Sep 15; 527(1):416-20. PubMed ID: 23816408
    [Abstract] [Full Text] [Related]

  • 11. Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathy.
    Waldmüller S, Sakthivel S, Saadi AV, Selignow C, Rakesh PG, Golubenko M, Joseph PK, Padmakumar R, Richard P, Schwartz K, Tharakan JM, Rajamanickam C, Vosberg HP.
    J Mol Cell Cardiol; 2003 Jun 15; 35(6):623-36. PubMed ID: 12788380
    [Abstract] [Full Text] [Related]

  • 12. A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy.
    Girolami F, Olivotto I, Passerini I, Zachara E, Nistri S, Re F, Fantini S, Baldini K, Torricelli F, Cecchi F.
    J Cardiovasc Med (Hagerstown); 2006 Aug 15; 7(8):601-7. PubMed ID: 16858239
    [Abstract] [Full Text] [Related]

  • 13. 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, Familial Cardiomyopathy Registry.
    Clin Transl Sci; 2013 Dec 15; 6(6):424-8. PubMed ID: 24119082
    [Abstract] [Full Text] [Related]

  • 14. [Relationship between systolic and diastolic function of the left ventricle in patients with impaired relaxation of the left ventricle without symptoms of heart failure. Attempt at quantitative estimation of diastolic function in the impaired relaxation stage].
    Kosmala W, Spring A, Witkowska M.
    Pol Arch Med Wewn; 1997 Nov 15; 98(11):414-23. PubMed ID: 9594559
    [Abstract] [Full Text] [Related]

  • 15. Predictor of left ventricular dysfunction after aortic valve replacement in mixed aortic valve disease.
    Egbe AC, Warnes CA.
    Int J Cardiol; 2017 Feb 01; 228():511-517. PubMed ID: 27875727
    [Abstract] [Full Text] [Related]

  • 16. Hypertrophic cardiomyopathy: two homozygous cases with "typical" hypertrophic cardiomyopathy and three new mutations in cases with progression to dilated cardiomyopathy.
    Nanni L, Pieroni M, Chimenti C, Simionati B, Zimbello R, Maseri A, Frustaci A, Lanfranchi G.
    Biochem Biophys Res Commun; 2003 Sep 19; 309(2):391-8. PubMed ID: 12951062
    [Abstract] [Full Text] [Related]

  • 17. Association of SNP Rs9943582 in APLNR with Left Ventricle Systolic Dysfunction in Patients with Coronary Artery Disease in a Chinese Han GeneID Population.
    Wang P, Xu C, Wang C, Wu Y, Wang D, Chen S, Zhao Y, Wang X, Li S, Yang Q, Zeng Q, Tu X, Liao Y, Wang QK, Cheng X.
    PLoS One; 2015 Sep 19; 10(5):e0125926. PubMed ID: 25993436
    [Abstract] [Full Text] [Related]

  • 18. Novel Phenotype-Genotype Correlations of Restrictive Cardiomyopathy With Myosin-Binding Protein C (MYBPC3) Gene Mutations Tested by Next-Generation Sequencing.
    Wu W, Lu CX, Wang YN, Liu F, Chen W, Liu YT, Han YC, Cao J, Zhang SY, Zhang X.
    J Am Heart Assoc; 2015 Jul 10; 4(7):. PubMed ID: 26163040
    [Abstract] [Full Text] [Related]

  • 19. Clinical outcomes associated with sarcomere mutations in hypertrophic cardiomyopathy: a meta-analysis on 7675 individuals.
    Sedaghat-Hamedani F, Kayvanpour E, Tugrul OF, Lai A, Amr A, Haas J, Proctor T, Ehlermann P, Jensen K, Katus HA, Meder B.
    Clin Res Cardiol; 2018 Jan 10; 107(1):30-41. PubMed ID: 28840316
    [Abstract] [Full Text] [Related]

  • 20. Screening of MYH7, MYBPC3, and TNNT2 genes in Brazilian patients with hypertrophic cardiomyopathy.
    Marsiglia JD, Credidio FL, de Oliveira TG, Reis RF, Antunes Mde O, de Araujo AQ, Pedrosa RP, Barbosa-Ferreira JM, Mady C, Krieger JE, Arteaga-Fernandez E, Pereira Ada C.
    Am Heart J; 2013 Oct 10; 166(4):775-82. PubMed ID: 24093860
    [Abstract] [Full Text] [Related]

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