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 *

157 related articles for article (PubMed ID: 16288990)

  • 1. Drastic Ca2+ sensitization of myofilament associated with a small structural change in troponin I in inherited restrictive cardiomyopathy.
    Yumoto F; Lu QW; Morimoto S; Tanaka H; Kono N; Nagata K; Ojima T; Takahashi-Yanaga F; Miwa Y; Sasaguri T; Nishita K; Tanokura M; Ohtsuki I
    Biochem Biophys Res Commun; 2005 Dec; 338(3):1519-26. PubMed ID: 16288990
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences.
    Doolan A; Tebo M; Ingles J; Nguyen L; Tsoutsman T; Lam L; Chiu C; Chung J; Weintraub RG; Semsarian C
    J Mol Cell Cardiol; 2005 Feb; 38(2):387-93. PubMed ID: 15698845
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in human cardiac troponin I that are associated with restrictive cardiomyopathy affect basal ATPase activity and the calcium sensitivity of force development.
    Gomes AV; Liang J; Potter JD
    J Biol Chem; 2005 Sep; 280(35):30909-15. PubMed ID: 15961398
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A mutation in the N-terminus of troponin I that is associated with hypertrophic cardiomyopathy affects the Ca(2+)-sensitivity, phosphorylation kinetics and proteolytic susceptibility of troponin.
    Gomes AV; Harada K; Potter JD
    J Mol Cell Cardiol; 2005 Nov; 39(5):754-65. PubMed ID: 16005017
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Restrictive Cardiomyopathy Troponin I R145W Mutation Does Not Perturb Myofilament Length-dependent Activation in Human Cardiac Sarcomeres.
    Dvornikov AV; Smolin N; Zhang M; Martin JL; Robia SL; de Tombe PP
    J Biol Chem; 2016 Oct; 291(41):21817-21828. PubMed ID: 27557662
    [TBL] [Abstract][Full Text] [Related]  

  • 6. PKC-betaII sensitizes cardiac myofilaments to Ca2+ by phosphorylating troponin I on threonine-144.
    Wang H; Grant JE; Doede CM; Sadayappan S; Robbins J; Walker JW
    J Mol Cell Cardiol; 2006 Nov; 41(5):823-33. PubMed ID: 17010989
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function?
    Willott RH; Gomes AV; Chang AN; Parvatiyar MS; Pinto JR; Potter JD
    J Mol Cell Cardiol; 2010 May; 48(5):882-92. PubMed ID: 19914256
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The dilated cardiomyopathy G159D mutation in cardiac troponin C weakens the anchoring interaction with troponin I.
    Baryshnikova OK; Robertson IM; Mercier P; Sykes BD
    Biochemistry; 2008 Oct; 47(41):10950-60. PubMed ID: 18803402
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pathogenesis associated with a restrictive cardiomyopathy mutant in cardiac troponin T is due to reduced protein stability and greatly increased myofilament Ca2+ sensitivity.
    Parvatiyar MS; Pinto JR
    Biochim Biophys Acta; 2015 Feb; 1850(2):365-72. PubMed ID: 25450489
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phosphorylation and mutation of human cardiac troponin I deferentially destabilize the interaction of the functional regions of troponin I with troponin C.
    Li MX; Wang X; Lindhout DA; Buscemi N; Van Eyk JE; Sykes BD
    Biochemistry; 2003 Dec; 42(49):14460-8. PubMed ID: 14661957
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Computational simulation of hypertrophic cardiomyopathy mutations in troponin I: influence of increased myofilament calcium sensitivity on isometric force, ATPase and [Ca2+]i.
    Kataoka A; Hemmer C; Chase PB
    J Biomech; 2007; 40(9):2044-52. PubMed ID: 17140583
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cardiac troponin C-L29Q, related to hypertrophic cardiomyopathy, hinders the transduction of the protein kinase A dependent phosphorylation signal from cardiac troponin I to C.
    Schmidtmann A; Lindow C; Villard S; Heuser A; Mügge A; Gessner R; Granier C; Jaquet K
    FEBS J; 2005 Dec; 272(23):6087-97. PubMed ID: 16302972
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Infantile restrictive cardiomyopathy: cTnI-R170G/W impair the interplay of sarcomeric proteins and the integrity of thin filaments.
    Cimiotti D; Fujita-Becker S; Möhner D; Smolina N; Budde H; Wies A; Morgenstern L; Gudkova A; Sejersen T; Sjöberg G; Mügge A; Nowaczyk MM; Reusch P; Pfitzer G; Stehle R; Schröder RR; Mannherz HG; Kostareva A; Jaquet K
    PLoS One; 2020; 15(3):e0229227. PubMed ID: 32182250
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Allele and species dependent contractile defects by restrictive and hypertrophic cardiomyopathy-linked troponin I mutants.
    Davis J; Wen H; Edwards T; Metzger JM
    J Mol Cell Cardiol; 2008 May; 44(5):891-904. PubMed ID: 18423659
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Restrictive cardiomyopathy mutations demonstrate functions of the C-terminal end-segment of troponin I.
    Akhter S; Bueltmann K; Huang X; Jin JP
    Arch Biochem Biophys; 2014 Jun; 552-553():3-10. PubMed ID: 24326031
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dilated cardiomyopathy mutant tropomyosin mice develop cardiac dysfunction with significantly decreased fractional shortening and myofilament calcium sensitivity.
    Rajan S; Ahmed RP; Jagatheesan G; Petrashevskaya N; Boivin GP; Urboniene D; Arteaga GM; Wolska BM; Solaro RJ; Liggett SB; Wieczorek DF
    Circ Res; 2007 Jul; 101(2):205-14. PubMed ID: 17556658
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular and cellular aspects of troponin cardiomyopathies.
    Gomes AV; Potter JD
    Ann N Y Acad Sci; 2004 May; 1015():214-24. PubMed ID: 15201162
    [TBL] [Abstract][Full Text] [Related]  

  • 18. C-terminal truncation of cardiac troponin I causes divergent effects on ATPase and force: implications for the pathophysiology of myocardial stunning.
    Foster DB; Noguchi T; VanBuren P; Murphy AM; Van Eyk JE
    Circ Res; 2003 Nov; 93(10):917-24. PubMed ID: 14551240
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Functional consequences of the mutations in human cardiac troponin I gene found in familial hypertrophic cardiomyopathy.
    Takahashi-Yanaga F; Morimoto S; Harada K; Minakami R; Shiraishi F; Ohta M; Lu QW; Sasaguri T; Ohtsuki I
    J Mol Cell Cardiol; 2001 Dec; 33(12):2095-107. PubMed ID: 11735257
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Structural mapping of single cysteine mutants of cardiac troponin I.
    Dong WJ; Xing J; Chandra M; Solaro J; Cheung HC
    Proteins; 2000 Dec; 41(4):438-47. PubMed ID: 11056032
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.