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 *

145 related articles for article (PubMed ID: 34193752)

  • 1. Multiple Vasculopathies and Heart Failure in Patient With ACTA-2 Mutation.
    Saito D; Nabeta T; Inoue N; Ishizue N; Ako J
    Circ J; 2021 Aug; 85(9):1588. PubMed ID: 34193752
    [No Abstract]   [Full Text] [Related]  

  • 2. Mutant vascular actin is a TAAD misbehaving.
    Rubenstein PA; Wen KK
    Proc Natl Acad Sci U S A; 2015 Aug; 112(31):9500-1. PubMed ID: 26204915
    [No Abstract]   [Full Text] [Related]  

  • 3. [Genetic aspects of chronic cardiac failure].
    Tereshchenko SN; Dzhaiani NA; Moiseev VS
    Ter Arkh; 2000; 72(4):75-7. PubMed ID: 10833807
    [No Abstract]   [Full Text] [Related]  

  • 4. Mutant ADA2 in vasculopathies.
    Segel R; King MC; Levy-Lahad E
    N Engl J Med; 2014 Jul; 371(5):481. PubMed ID: 25083540
    [No Abstract]   [Full Text] [Related]  

  • 5. Mutant ADA2 in vasculopathies.
    Van Eyck L; Liston A; Wouters C
    N Engl J Med; 2014 Jul; 371(5):480. PubMed ID: 25075848
    [No Abstract]   [Full Text] [Related]  

  • 6. Mutant ADA2 in vasculopathies.
    Bras J; Guerreiro R; Santo GC
    N Engl J Med; 2014 Jul; 371(5):478-80. PubMed ID: 25075847
    [No Abstract]   [Full Text] [Related]  

  • 7. Mutant ADA2 in vasculopathies.
    Van Eyck L; Liston A; Meyts I
    N Engl J Med; 2014 Jul; 371(5):478-9. PubMed ID: 25075846
    [No Abstract]   [Full Text] [Related]  

  • 8. Mutant ADA2 in vasculopathies.
    van Montfrans J; Zavialov A; Zhou Q
    N Engl J Med; 2014 Jul; 371(5):478. PubMed ID: 25075845
    [No Abstract]   [Full Text] [Related]  

  • 9. Mutant ADA2 in vasculopathies.
    Kastner DL; Zhou Q; Aksentijevich I
    N Engl J Med; 2014 Jul; 371(5):480-1. PubMed ID: 25075844
    [No Abstract]   [Full Text] [Related]  

  • 10. Migraine and genetic and acquired vasculopathies.
    Stam AH; Haan J; van den Maagdenberg AM; Ferrari MD; Terwindt GM
    Cephalalgia; 2009 Sep; 29(9):1006-17. PubMed ID: 19689610
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Modifications of myocardial protein phenotype in cardiac hypertrophy and failure].
    Mercadier JJ; Schwartz K
    C R Seances Soc Biol Fil; 1990; 184(5-6):297-309. PubMed ID: 2151803
    [No Abstract]   [Full Text] [Related]  

  • 12. Vascular disease-causing mutation R258C in ACTA2 disrupts actin dynamics and interaction with myosin.
    Lu H; Fagnant PM; Bookwalter CS; Joel P; Trybus KM
    Proc Natl Acad Sci U S A; 2015 Aug; 112(31):E4168-77. PubMed ID: 26153420
    [TBL] [Abstract][Full Text] [Related]  

  • 13. α-Smooth Muscle Actin and ACTA2 Gene Expressions in Vasculopathies.
    Yuan SM
    Braz J Cardiovasc Surg; 2015; 30(6):644-9. PubMed ID: 26934405
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Genetic variants promoting smooth muscle cell proliferation can result in diffuse and diverse vascular diseases: evidence for a hyperplastic vasculomyopathy.
    Milewicz DM; Kwartler CS; Papke CL; Regalado ES; Cao J; Reid AJ
    Genet Med; 2010 Apr; 12(4):196-203. PubMed ID: 20130469
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association of MTHFR A1298C polymorphism (but not of MTHFR C677T) with elevated homocysteine levels and placental vasculopathies.
    Klai S; Fekih-Mrissa N; El Housaini S; Kaabechi N; Nsiri B; Rachdi R; Gritli N
    Blood Coagul Fibrinolysis; 2011 Jul; 22(5):374-8. PubMed ID: 21577095
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dilated cardiomyopathy mutation in the converter domain of human cardiac myosin alters motor activity and response to omecamtiv mecarbil.
    Tang W; Unrath WC; Desetty R; Yengo CM
    J Biol Chem; 2019 Nov; 294(46):17314-17325. PubMed ID: 31578282
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Establishment of Specialized Clinical Cardiovascular Genetics Programs: Recognizing the Need and Meeting Standards: A Scientific Statement From the American Heart Association.
    Ahmad F; McNally EM; Ackerman MJ; Baty LC; Day SM; Kullo IJ; Madueme PC; Maron MS; Martinez MW; Salberg L; Taylor MR; Wilcox JE
    Circ Genom Precis Med; 2019 Jun; 12(6):e000054. PubMed ID: 31117808
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sarcomere mutations in cardiogenesis and ventricular noncompaction.
    McNally E; Dellefave L
    Trends Cardiovasc Med; 2009 Jan; 19(1):17-21. PubMed ID: 19467449
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Multiple vasculopathies and hepatitis B in a family.
    Mooradian AD; Frayha R
    Br J Rheumatol; 1985 Feb; 24(1):19-23. PubMed ID: 2858241
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.