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 *

388 related articles for article (PubMed ID: 25651172)

  • 1. The genetic landscape of cardiomyopathy and its role in heart failure.
    McNally EM; Barefield DY; Puckelwartz MJ
    Cell Metab; 2015 Feb; 21(2):174-182. PubMed ID: 25651172
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Zebrafish heart failure models: opportunities and challenges.
    Shi X; Chen R; Zhang Y; Yun J; Brand-Arzamendi K; Liu X; Wen XY
    Amino Acids; 2018 Jul; 50(7):787-798. PubMed ID: 29725858
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes.
    Xu Q; Dewey S; Nguyen S; Gomes AV
    J Mol Cell Cardiol; 2010 May; 48(5):899-909. PubMed ID: 20298698
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Essential light chain S195 phosphorylation is required for cardiac adaptation under physical stress.
    Scheid LM; Mosqueira M; Hein S; Kossack M; Juergensen L; Mueller M; Meder B; Fink RH; Katus HA; Hassel D
    Cardiovasc Res; 2016 Jul; 111(1):44-55. PubMed ID: 27013636
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Targeted therapies in genetic dilated and hypertrophic cardiomyopathies: from molecular mechanisms to therapeutic targets. A position paper from the Heart Failure Association (HFA) and the Working Group on Myocardial Function of the European Society of Cardiology (ESC).
    de Boer RA; Heymans S; Backs J; Carrier L; Coats AJS; Dimmeler S; Eschenhagen T; Filippatos G; Gepstein L; Hulot JS; Knöll R; Kupatt C; Linke WA; Seidman CE; Tocchetti CG; van der Velden J; Walsh R; Seferovic PM; Thum T
    Eur J Heart Fail; 2022 Mar; 24(3):406-420. PubMed ID: 34969177
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Implications of protease activation in cardiac dysfunction and development of genetic cardiomyopathy in hamsters.
    Müller AL; Freed D; Hryshko L; Dhalla NS
    Can J Physiol Pharmacol; 2012 Aug; 90(8):995-1004. PubMed ID: 22784245
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. [Familial idiopathic cardiomyopathy].
    Petrov D
    Vutr Boles; 1982; 21(4):96-9. PubMed ID: 7147927
    [No Abstract]   [Full Text] [Related]  

  • 10. Amplification of lipotoxic cardiomyopathy in the VDR gene knockout mouse.
    Glenn DJ; Cardema MC; Gardner DG
    J Steroid Biochem Mol Biol; 2016 Nov; 164():292-298. PubMed ID: 26429397
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genes and their polymorphisms in mono- and multifactorial cardiomyopathies: towards pharmacogenomics in heart failure.
    Charron P; Komajda M
    Pharmacogenomics; 2002 May; 3(3):367-78. PubMed ID: 12052144
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Familial cardiomyopathy.
    Mysik M; Dubiel JP
    Acta Med Pol; 1973; 14(4):323-31. PubMed ID: 4763197
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. A genome-wide analysis of cardiac lesions of pigs that die during transport: Is heart failure of in-transit-loss pigs associated with a heritable cardiomyopathy?
    Zurbrigg K; Bertolini F; Walugembe M; van Dreumel T; Alves D; Friendship R; O'Sullivan TL; Rothschild MF
    Can J Vet Res; 2021 Apr; 85(2):119-126. PubMed ID: 33883819
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Role of neuropeptides in cardiomyopathies.
    Dvorakova MC; Kruzliak P; Rabkin SW
    Peptides; 2014 Nov; 61():1-6. PubMed ID: 25149360
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The molecular and cellular biology of heart failure.
    Mayer NJ; Rubin SA
    Curr Opin Cardiol; 1995 May; 10(3):238-45. PubMed ID: 7612972
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary dysrhythmic congestive cardiomyopathy.
    Brink AJ; Torrington M; van der Walt JJ
    S Afr Med J; 1976 Dec; 50(54):2119-23. PubMed ID: 1006490
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Autophagy in desmin-related cardiomyopathy: thoughts at the halfway point.
    Maloyan A; Robbins J
    Autophagy; 2010 Jul; 6(5):665-6. PubMed ID: 20523125
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.