BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

238 related articles for article (PubMed ID: 9172070)

  • 1. The in vitro motility activity of beta-cardiac myosin depends on the nature of the beta-myosin heavy chain gene mutation in hypertrophic cardiomyopathy.
    Cuda G; Fananapazir L; Epstein ND; Sellers JR
    J Muscle Res Cell Motil; 1997 Jun; 18(3):275-83. PubMed ID: 9172070
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Functional analysis of myosin mutations that cause familial hypertrophic cardiomyopathy.
    Roopnarine O; Leinwand LA
    Biophys J; 1998 Dec; 75(6):3023-30. PubMed ID: 9826622
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hypertrophic cardiomyopathy R403Q mutation in rabbit β-myosin reduces contractile function at the molecular and myofibrillar levels.
    Lowey S; Bretton V; Joel PB; Trybus KM; Gulick J; Robbins J; Kalganov A; Cornachione AS; Rassier DE
    Proc Natl Acad Sci U S A; 2018 Oct; 115(44):11238-11243. PubMed ID: 30322937
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Single-molecule mechanics of R403Q cardiac myosin isolated from the mouse model of familial hypertrophic cardiomyopathy.
    Tyska MJ; Hayes E; Giewat M; Seidman CE; Seidman JG; Warshaw DM
    Circ Res; 2000 Apr; 86(7):737-44. PubMed ID: 10764406
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy.
    Fananapazir L; Dalakas MC; Cyran F; Cohn G; Epstein ND
    Proc Natl Acad Sci U S A; 1993 May; 90(9):3993-7. PubMed ID: 8483915
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cardiac and skeletal muscle expression of mutant β-myosin heavy chains, degree of functional impairment and phenotypic heterogeneity in hypertrophic cardiomyopathy.
    Di Domenico M; Casadonte R; Ricci P; Santini M; Frati G; Rizzo A; Carratelli CR; Lamberti M; Parrotta E; Quaresima B; Faniello CM; Costanzo F; Cuda G
    J Cell Physiol; 2012 Oct; 227(10):3471-6. PubMed ID: 22213221
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Isometric tension and mutant myosin heavy chain content in single skeletal myofibers from hypertrophic cardiomyopathy patients.
    Malinchik S; Cuda G; Podolsky RJ; Horowits R
    J Mol Cell Cardiol; 1997 Feb; 29(2):667-76. PubMed ID: 9140824
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Skeletal muscle expression and abnormal function of beta-myosin in hypertrophic cardiomyopathy.
    Cuda G; Fananapazir L; Zhu WS; Sellers JR; Epstein ND
    J Clin Invest; 1993 Jun; 91(6):2861-5. PubMed ID: 8514894
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Functional consequences of mutations in the smooth muscle myosin heavy chain at sites implicated in familial hypertrophic cardiomyopathy.
    Yamashita H; Tyska MJ; Warshaw DM; Lowey S; Trybus KM
    J Biol Chem; 2000 Sep; 275(36):28045-52. PubMed ID: 10882745
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prognostic significance of beta-myosin heavy chain mutations is reflective of their hypertrophic expressivity in patients with hypertrophic cardiomyopathy.
    Abchee A; Marian AJ
    J Investig Med; 1997 Apr; 45(4):191-6. PubMed ID: 9154300
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation.
    Overeem S; Schelhaas HJ; Blijham PJ; Grootscholten MI; ter Laak HJ; Timmermans J; van den Wijngaard A; Zwarts MJ
    Neuromuscul Disord; 2007 Jun; 17(6):490-3. PubMed ID: 17383184
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [An analysis of the prevalence of the Arg403Gln, Gly584Arg and Leu908Val mutations in the beta-myosin heavy chain in Portuguese patients who are carriers of familial hypertrophic cardiomyopathy].
    Vieira M; Gonçalves L; Ventura M; Vieira M; Providência LA; Pires E; Faro C
    Rev Port Cardiol; 1995 Oct; 14(10):733-5. PubMed ID: 7492407
    [No Abstract]   [Full Text] [Related]  

  • 13. Molecular basis of hypertrophic and dilated cardiomyopathy.
    Marian AJ; Roberts R
    Tex Heart Inst J; 1994; 21(1):6-15. PubMed ID: 8180512
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The molecular biology and pathophysiology of hypertrophic cardiomyopathy due to mutations in the beta myosin heavy chains and the essential and regulatory light chains.
    Epstein ND
    Adv Exp Med Biol; 1998; 453():105-14; discussion 114-5. PubMed ID: 9889820
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Myosin mutations in hypertrophic cardiomyopathy and functional implications.
    Vosberg HP
    Herz; 1994 Apr; 19(2):75-83. PubMed ID: 8194835
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular and phenotypic effects of heterozygous, homozygous, and compound heterozygote myosin heavy-chain mutations.
    Alpert NR; Mohiddin SA; Tripodi D; Jacobson-Hatzell J; Vaughn-Whitley K; Brosseau C; Warshaw DM; Fananapazir L
    Am J Physiol Heart Circ Physiol; 2005 Mar; 288(3):H1097-102. PubMed ID: 15528230
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Abnormal contractile properties of muscle fibers expressing beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy.
    Lankford EB; Epstein ND; Fananapazir L; Sweeney HL
    J Clin Invest; 1995 Mar; 95(3):1409-14. PubMed ID: 7883988
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A Failure to Communicate: MYOSIN RESIDUES INVOLVED IN HYPERTROPHIC CARDIOMYOPATHY AFFECT INTER-DOMAIN INTERACTION.
    Kronert WA; Melkani GC; Melkani A; Bernstein SI
    J Biol Chem; 2015 Dec; 290(49):29270-80. PubMed ID: 26446785
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy.
    Rayment I; Holden HM; Sellers JR; Fananapazir L; Epstein ND
    Proc Natl Acad Sci U S A; 1995 Apr; 92(9):3864-8. PubMed ID: 7731997
    [TBL] [Abstract][Full Text] [Related]  

  • 20. β-Cardiac myosin hypertrophic cardiomyopathy mutations release sequestered heads and increase enzymatic activity.
    Adhikari AS; Trivedi DV; Sarkar SS; Song D; Kooiker KB; Bernstein D; Spudich JA; Ruppel KM
    Nat Commun; 2019 Jun; 10(1):2685. PubMed ID: 31213605
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.