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 *

310 related articles for article (PubMed ID: 25503402)

  • 1. A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias.
    Yuan F; Qiu XB; Li RG; Qu XK; Wang J; Xu YJ; Liu X; Fang WY; Yang YQ; Liao DN
    Int J Mol Med; 2015 Feb; 35(2):478-86. PubMed ID: 25503402
    [TBL] [Abstract][Full Text] [Related]  

  • 2. TBX20 loss-of-function mutation associated with familial dilated cardiomyopathy.
    Zhao CM; Bing-Sun ; Song HM; Wang J; Xu WJ; Jiang JF; Qiu XB; Yuan F; Xu JH; Yang YQ
    Clin Chem Lab Med; 2016 Feb; 54(2):325-32. PubMed ID: 26118961
    [TBL] [Abstract][Full Text] [Related]  

  • 3. GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy.
    Li RG; Li L; Qiu XB; Yuan F; Xu L; Li X; Xu YJ; Jiang WF; Jiang JQ; Liu X; Fang WY; Zhang M; Peng LY; Qu XK; Yang YQ
    Biochem Biophys Res Commun; 2013 Oct; 439(4):591-6. PubMed ID: 24041700
    [TBL] [Abstract][Full Text] [Related]  

  • 4. TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy.
    Zhang XL; Qiu XB; Yuan F; Wang J; Zhao CM; Li RG; Xu L; Xu YJ; Shi HY; Hou XM; Qu XK; Xu YW; Yang YQ
    Biochem Biophys Res Commun; 2015 Mar; 459(1):166-71. PubMed ID: 25725155
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prevalence and spectrum of GATA4 mutations associated with sporadic dilated cardiomyopathy.
    Li J; Liu WD; Yang ZL; Yuan F; Xu L; Li RG; Yang YQ
    Gene; 2014 Sep; 548(2):174-81. PubMed ID: 25017055
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel GATA4 loss-of-function mutation responsible for familial dilated cardiomyopathy.
    Zhao L; Xu JH; Xu WJ; Yu H; Wang Q; Zheng HZ; Jiang WF; Jiang JF; Yang YQ
    Int J Mol Med; 2014 Mar; 33(3):654-60. PubMed ID: 24366163
    [TBL] [Abstract][Full Text] [Related]  

  • 7. GATA5 loss-of-function mutation in familial dilated cardiomyopathy.
    Zhang XL; Dai N; Tang K; Chen YQ; Chen W; Wang J; Zhao CM; Yuan F; Qiu XB; Qu XK; Yang YQ; Xu YW
    Int J Mol Med; 2015 Mar; 35(3):763-70. PubMed ID: 25543888
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy.
    Xu JH; Gu JY; Guo YH; Zhang H; Qiu XB; Li RG; Shi HY; Liu H; Yang XX; Xu YJ; Qu XK; Yang YQ
    Int Heart J; 2017 Aug; 58(4):521-529. PubMed ID: 28690296
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation.
    Huang RT; Xue S; Xu YJ; Zhou M; Yang YQ
    Int J Mol Med; 2013 May; 31(5):1119-26. PubMed ID: 23525379
    [TBL] [Abstract][Full Text] [Related]  

  • 10. NKX2-6 mutation predisposes to familial atrial fibrillation.
    Wang J; Zhang DF; Sun YM; Li RG; Qiu XB; Qu XK; Liu X; Fang WY; Yang YQ
    Int J Mol Med; 2014 Dec; 34(6):1581-90. PubMed ID: 25319568
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation.
    Xie WH; Chang C; Xu YJ; Li RG; Qu XK; Fang WY; Liu X; Yang YQ
    Clinics (Sao Paulo); 2013 Jun; 68(6):777-84. PubMed ID: 23778487
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy.
    Qiu XB; Qu XK; Li RG; Liu H; Xu YJ; Zhang M; Shi HY; Hou XM; Liu X; Yuan F; Sun YM; Wang J; Huang RT; Xue S; Yang YQ
    Clin Chem Lab Med; 2017 Aug; 55(9):1417-1425. PubMed ID: 28099117
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel TBX5 loss-of-function mutation associated with sporadic dilated cardiomyopathy.
    Zhou W; Zhao L; Jiang JQ; Jiang WF; Yang YQ; Qiu XB
    Int J Mol Med; 2015 Jul; 36(1):282-8. PubMed ID: 25963046
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel NKX2-5 mutation in familial ventricular septal defect.
    Wang J; Xin YF; Liu XY; Liu ZM; Wang XZ; Yang YQ
    Int J Mol Med; 2011 Mar; 27(3):369-75. PubMed ID: 21165553
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prevalence and spectrum of LRRC10 mutations associated with idiopathic dilated cardiomyopathy.
    Qu XK; Yuan F; Li RG; Xu L; Jing WF; Liu H; Xu YJ; Zhang M; Liu X; Fang WY; Yang YQ; Qiu XB
    Mol Med Rep; 2015 Sep; 12(3):3718-3724. PubMed ID: 26017719
    [TBL] [Abstract][Full Text] [Related]  

  • 16. GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy.
    Xu L; Zhao L; Yuan F; Jiang WF; Liu H; Li RG; Xu YJ; Zhang M; Fang WY; Qu XK; Yang YQ; Qiu XB
    Int J Mol Med; 2014 Nov; 34(5):1315-22. PubMed ID: 25119427
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel TBX20 loss‑of‑function mutation contributes to adult‑onset dilated cardiomyopathy or congenital atrial septal defect.
    Zhou YM; Dai XY; Huang RT; Xue S; Xu YJ; Qiu XB; Yang YQ
    Mol Med Rep; 2016 Oct; 14(4):3307-14. PubMed ID: 27510170
    [TBL] [Abstract][Full Text] [Related]  

  • 18. HAND1 loss-of-function mutation associated with familial dilated cardiomyopathy.
    Zhou YM; Dai XY; Qiu XB; Yuan F; Li RG; Xu YJ; Qu XK; Huang RT; Xue S; Yang YQ
    Clin Chem Lab Med; 2016 Jul; 54(7):1161-7. PubMed ID: 26581070
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel NKX2.6 mutation associated with congenital ventricular septal defect.
    Wang J; Mao JH; Ding KK; Xu WJ; Liu XY; Qiu XB; Li RG; Qu XK; Xu YJ; Huang RT; Xue S; Yang YQ
    Pediatr Cardiol; 2015 Mar; 36(3):646-56. PubMed ID: 25380965
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation.
    Yu H; Xu JH; Song HM; Zhao L; Xu WJ; Wang J; Li RG; Xu L; Jiang WF; Qiu XB; Jiang JQ; Qu XK; Liu X; Fang WY; Jiang JF; Yang YQ
    Int J Med Sci; 2014; 11(6):554-63. PubMed ID: 24782644
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.