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 *

174 related articles for article (PubMed ID: 11701629)

  • 1. From the sarcomere to the nucleus: role of genetics and signaling in structural heart disease.
    Nicol RL; Frey N; Olson EN
    Annu Rev Genomics Hum Genet; 2000; 1():179-223. PubMed ID: 11701629
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The genetic basis for cardiac remodeling.
    Ahmad F; Seidman JG; Seidman CE
    Annu Rev Genomics Hum Genet; 2005; 6():185-216. PubMed ID: 16124859
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cardiac sarcomeric function, small G-protein signaling, and heart failure.
    Vahebi S; Solaro RJ
    Panminerva Med; 2005 Sep; 47(3):133-42. PubMed ID: 16462722
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Calcineurin-NFAT signaling regulates the cardiac hypertrophic response in coordination with the MAPKs.
    Molkentin JD
    Cardiovasc Res; 2004 Aug; 63(3):467-75. PubMed ID: 15276472
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Adrenergic pathways and left ventricular remodeling.
    Dorn GW
    J Card Fail; 2002 Dec; 8(6 Suppl):S370-3. PubMed ID: 12555147
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A straightforward guide to the sarcomeric basis of cardiomyopathies.
    Lopes LR; Elliott PM
    Heart; 2014 Dec; 100(24):1916-23. PubMed ID: 25271316
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular mechanisms in cardiomyopathy.
    Dadson K; Hauck L; Billia F
    Clin Sci (Lond); 2017 Jul; 131(13):1375-1392. PubMed ID: 28645928
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular mechanisms of inherited cardiomyopathies.
    Fatkin D; Graham RM
    Physiol Rev; 2002 Oct; 82(4):945-80. PubMed ID: 12270949
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Hereditary cardiomyopathies: a review. Mutation of structural proteins a common cause of hereditary cardiomyopathy].
    Sjöberg G; Kostareva A; Sejersen T
    Lakartidningen; 2005 Mar 14-20; 102(11):845-7, 850-3. PubMed ID: 15835520
    [TBL] [Abstract][Full Text] [Related]  

  • 11. G-proteins in growth and apoptosis: lessons from the heart.
    Adams JW; Brown JH
    Oncogene; 2001 Mar; 20(13):1626-34. PubMed ID: 11313910
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cardiomyopathy: molecular and immunological aspects (review).
    Takeda N
    Int J Mol Med; 2003 Jan; 11(1):13-6. PubMed ID: 12469210
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Review: genetics of familial dilated cardiomyopathy].
    Amara ME; Villard E; Komajda M
    Ann Cardiol Angeiol (Paris); 2005 Jun; 54(3):151-6. PubMed ID: 15991472
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Direct and indirect interactions between calcineurin-NFAT and MEK1-extracellular signal-regulated kinase 1/2 signaling pathways regulate cardiac gene expression and cellular growth.
    Sanna B; Bueno OF; Dai YS; Wilkins BJ; Molkentin JD
    Mol Cell Biol; 2005 Feb; 25(3):865-78. PubMed ID: 15657416
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Novel locus for an inherited cardiomyopathy maps to chromosome 7.
    Song L; DePalma SR; Kharlap M; Zenovich AG; Cirino A; Mitchell R; McDonough B; Maron BJ; Seidman CE; Seidman JG; Ho CY
    Circulation; 2006 May; 113(18):2186-92. PubMed ID: 16651466
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Troponin and cardiomyopathy.
    Chang AN; Parvatiyar MS; Potter JD
    Biochem Biophys Res Commun; 2008 Apr; 369(1):74-81. PubMed ID: 18157941
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.