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 *

138 related articles for article (PubMed ID: 18391120)

  • 1. Disease-modifying mutations in familial hypertrophic cardiomyopathy: complexity from simplicity.
    Hilfiker-Kleiner D; Knöll R
    Circulation; 2008 Apr; 117(14):1775-7. PubMed ID: 18391120
    [No Abstract]   [Full Text] [Related]  

  • 2. Severe heart failure and early mortality in a double-mutation mouse model of familial hypertrophic cardiomyopathy.
    Tsoutsman T; Kelly M; Ng DC; Tan JE; Tu E; Lam L; Bogoyevitch MA; Seidman CE; Seidman JG; Semsarian C
    Circulation; 2008 Apr; 117(14):1820-31. PubMed ID: 18362229
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Molecular insights from a novel cardiac troponin I mouse model of familial hypertrophic cardiomyopathy.
    Tsoutsman T; Chung J; Doolan A; Nguyen L; Williams IA; Tu E; Lam L; Bailey CG; Rasko JE; Allen DG; Semsarian C
    J Mol Cell Cardiol; 2006 Oct; 41(4):623-32. PubMed ID: 16950368
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lys184 deletion in troponin I impairs relaxation kinetics and induces hypercontractility in murine cardiac myofibrils.
    Iorga B; Blaudeck N; Solzin J; Neulen A; Stehle I; Lopez Davila AJ; Pfitzer G; Stehle R
    Cardiovasc Res; 2008 Mar; 77(4):676-86. PubMed ID: 18096573
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model.
    Semsarian C; Ahmad I; Giewat M; Georgakopoulos D; Schmitt JP; McConnell BK; Reiken S; Mende U; Marks AR; Kass DA; Seidman CE; Seidman JG
    J Clin Invest; 2002 Apr; 109(8):1013-20. PubMed ID: 11956238
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy.
    Semsarian C; Healey MJ; Fatkin D; Giewat M; Duffy C; Seidman CE; Seidman JG
    J Mol Cell Cardiol; 2001 Nov; 33(11):2055-60. PubMed ID: 11708849
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hypertrophy, fibrosis, and sudden cardiac death in response to pathological stimuli in mice with mutations in cardiac troponin T.
    Maass AH; Ikeda K; Oberdorf-Maass S; Maier SK; Leinwand LA
    Circulation; 2004 Oct; 110(15):2102-9. PubMed ID: 15466629
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Heart disease. How to subdue a swelling heart.
    Marx J
    Science; 2003 Jun; 300(5625):1492-6. PubMed ID: 12791957
    [No Abstract]   [Full Text] [Related]  

  • 10. A novel beta-myosin heavy chain gene mutation, p.Met531Arg, identified in isolated left ventricular non-compaction in humans, results in left ventricular hypertrophy that progresses to dilation in a mouse model.
    Kaneda T; Naruse C; Kawashima A; Fujino N; Oshima T; Namura M; Nunoda S; Mori S; Konno T; Ino H; Yamagishi M; Asano M
    Clin Sci (Lond); 2008 Mar; 114(6):431-40. PubMed ID: 17956225
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Knock-in mouse model of dilated cardiomyopathy caused by troponin mutation.
    Du CK; Morimoto S; Nishii K; Minakami R; Ohta M; Tadano N; Lu QW; Wang YY; Zhan DY; Mochizuki M; Kita S; Miwa Y; Takahashi-Yanaga F; Iwamoto T; Ohtsuki I; Sasaguri T
    Circ Res; 2007 Jul; 101(2):185-94. PubMed ID: 17556660
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Beta-myosin heavy chain gene mutations in familial hypertrophic cardiomyopathy: the usual suspect?
    McNally EM
    Circ Res; 2002 Feb; 90(3):246-7. PubMed ID: 11861410
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. Sarcomere protein gene mutations and inherited heart disease: a beta-cardiac myosin heavy chain mutation causing endocardial fibroelastosis and heart failure.
    Kamisago M; Schmitt JP; McNamara D; Seidman C; Seidman JG
    Novartis Found Symp; 2006; 274():176-89; discussion 189-95, 272-6. PubMed ID: 17019812
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Familial hypertrophic cardiomyopathy--a case report].
    Domal-Kwiatkowska D; Glanowska G; Smolik S; Wilczewski P; Mazurek U; Nowalany-Kozielska E; Fudal M; Wodniecki J
    Kardiol Pol; 2006 Nov; 64(11):1287-91. PubMed ID: 17165166
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes.
    Kaski JP; Syrris P; Burch M; Tomé-Esteban MT; Fenton M; Christiansen M; Andersen PS; Sebire N; Ashworth M; Deanfield JE; McKenna WJ; Elliott PM
    Heart; 2008 Nov; 94(11):1478-84. PubMed ID: 18467357
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inherited cardiomyopathies as a troponin disease.
    Harada K; Morimoto S
    Jpn J Physiol; 2004 Aug; 54(4):307-18. PubMed ID: 15631686
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A switch that lowers the betaAR: insights from a troponin I mutation linked to hypertrophic cardiomyopathy.
    Westfall MV
    J Mol Cell Cardiol; 2006 Jan; 40(1):10-2. PubMed ID: 16321398
    [No Abstract]   [Full Text] [Related]  

  • 19. IMAGE CARDIO MED: Inducible malignant ventricular tachyarrhythmia in a patient with genotyped hypertrophic cardiomyopathy in absence of left ventricular hypertrophy or enlargement.
    Ariyarajah V; Tam JW; Khadem A
    Circulation; 2009 Jun; 119(21):e543-4. PubMed ID: 19487599
    [No Abstract]   [Full Text] [Related]  

  • 20. Expanded spectrum of gene causing both hypertrophic cardiomyopathy and dilated cardiomyopathy.
    Morimoto S
    Circ Res; 2009 Aug; 105(4):313-5. PubMed ID: 19679850
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.