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 *

237 related articles for article (PubMed ID: 22407241)

  • 1. A novel GATA6 mutation associated with congenital ventricular septal defect.
    Zheng GF; Wei D; Zhao H; Zhou N; Yang YQ; Liu XY
    Int J Mol Med; 2012 Jun; 29(6):1065-71. PubMed ID: 22407241
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel GATA4 mutation responsible for congenital ventricular septal defects.
    Wang J; Fang M; Liu XY; Xin YF; Liu ZM; Chen XZ; Wang XZ; Fang WY; Liu X; Yang YQ
    Int J Mol Med; 2011 Oct; 28(4):557-64. PubMed ID: 21637914
    [TBL] [Abstract][Full Text] [Related]  

  • 3. GATA6 loss-of-function mutation in atrial fibrillation.
    Yang YQ; Li L; Wang J; Zhang XL; Li RG; Xu YJ; Tan HW; Wang XH; Jiang JQ; Fang WY; Liu X
    Eur J Med Genet; 2012 Oct; 55(10):520-6. PubMed ID: 22750565
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Novel GATA4 mutations in patients with congenital ventricular septal defects.
    Yang YQ; Wang J; Liu XY; Chen XZ; Zhang W; Wang XZ; Liu X; Fang WY
    Med Sci Monit; 2012 Jun; 18(6):CR344-50. PubMed ID: 22648249
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Involvement of a novel GATA4 mutation in atrial septal defects.
    Liu XY; Wang J; Zheng JH; Bai K; Liu ZM; Wang XZ; Liu X; Fang WY; Yang YQ
    Int J Mol Med; 2011 Jul; 28(1):17-23. PubMed ID: 21373748
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. TBX20 loss-of-function mutation contributes to double outlet right ventricle.
    Pan Y; Geng R; Zhou N; Zheng GF; Zhao H; Wang J; Zhao CM; Qiu XB; Yang YQ; Liu XY
    Int J Mol Med; 2015 Apr; 35(4):1058-66. PubMed ID: 25625280
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel GATA4 loss-of-function mutation associated with congenital ventricular septal defect.
    Yang YQ; Li L; Wang J; Liu XY; Chen XZ; Zhang W; Wang XZ; Jiang JQ; Liu X; Fang WY
    Pediatr Cardiol; 2012 Apr; 33(4):539-46. PubMed ID: 22101736
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CASZ1 loss-of-function mutation associated with congenital heart disease.
    Huang RT; Xue S; Wang J; Gu JY; Xu JH; Li YJ; Li N; Yang XX; Liu H; Zhang XD; Qu XK; Xu YJ; Qiu XB; Li RG; Yang YQ
    Gene; 2016 Dec; 595(1):62-68. PubMed ID: 27693370
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of fallot.
    Wang J; Luo XJ; Xin YF; Liu Y; Liu ZM; Wang Q; Li RG; Fang WY; Wang XZ; Yang YQ
    DNA Cell Biol; 2012 Nov; 31(11):1610-7. PubMed ID: 23020118
    [TBL] [Abstract][Full Text] [Related]  

  • 13. GATA5 loss-of-function mutation responsible for the congenital ventriculoseptal defect.
    Wei D; Bao H; Zhou N; Zheng GF; Liu XY; Yang YQ
    Pediatr Cardiol; 2013 Mar; 34(3):504-11. PubMed ID: 22961344
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.
    Sun YM; Wang J; Qiu XB; Yuan F; Li RG; Xu YJ; Qu XK; Shi HY; Hou XM; Huang RT; Xue S; Yang YQ
    G3 (Bethesda); 2016 Apr; 6(4):987-92. PubMed ID: 26865696
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve.
    Xu YJ; Di RM; Qiao Q; Li XM; Huang RT; Xue S; Liu XY; Wang J; Yang YQ
    Gene; 2018 Jul; 663():115-120. PubMed ID: 29653232
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel GATA6 loss-of-function mutation responsible for familial atrial fibrillation.
    Li J; Liu WD; Yang ZL; Yang YQ
    Int J Mol Med; 2012 Oct; 30(4):783-90. PubMed ID: 22824924
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Somatic mutations in the GATA6 gene underlie sporadic tetralogy of Fallot.
    Huang RT; Xue S; Xu YJ; Yang YQ
    Int J Mol Med; 2013 Jan; 31(1):51-8. PubMed ID: 23175051
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart Disease.
    Pan Y; Wang ZG; Liu XY; Zhao H; Zhou N; Zheng GF; Qiu XB; Li RG; Yuan F; Shi HY; Hou XM; Yang YQ
    Pediatr Cardiol; 2015 Oct; 36(7):1400-10. PubMed ID: 25860641
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.