BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

203 related articles for article (PubMed ID: 23289003)

  • 1. GATA5 loss-of-function mutations underlie tetralogy of fallot.
    Wei D; Bao H; Liu XY; Zhou N; Wang Q; Li RG; Xu YJ; Yang YQ
    Int J Med Sci; 2013; 10(1):34-42. PubMed ID: 23289003
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Somatic GATA5 mutations in sporadic tetralogy of Fallot.
    Huang RT; Xue S; Xu YJ; Zhou M; Yang YQ
    Int J Mol Med; 2014 May; 33(5):1227-35. PubMed ID: 24573614
    [TBL] [Abstract][Full Text] [Related]  

  • 3. GATA4 loss-of-function mutations underlie familial tetralogy of fallot.
    Yang YQ; Gharibeh L; Li RG; Xin YF; Wang J; Liu ZM; Qiu XB; Xu YJ; Xu L; Qu XK; Liu X; Fang WY; Huang RT; Xue S; Nemer G
    Hum Mutat; 2013 Dec; 34(12):1662-71. PubMed ID: 24000169
    [TBL] [Abstract][Full Text] [Related]  

  • 4. HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot.
    Wang J; Hu XQ; Guo YH; Gu JY; Xu JH; Li YJ; Li N; Yang XX; Yang YQ
    Pediatr Cardiol; 2017 Mar; 38(3):547-557. PubMed ID: 27942761
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation.
    Wang XH; Huang CX; Wang Q; Li RG; Xu YJ; Liu X; Fang WY; Yang YQ
    Int J Mol Med; 2013 Jan; 31(1):43-50. PubMed ID: 23175127
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation.
    Gu JY; Xu JH; Yu H; Yang YQ
    Clinics (Sao Paulo); 2012 Dec; 67(12):1393-9. PubMed ID: 23295592
    [TBL] [Abstract][Full Text] [Related]  

  • 8. GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve.
    Shi LM; Tao JW; Qiu XB; Wang J; Yuan F; Xu L; Liu H; Li RG; Xu YJ; Wang Q; Zheng HZ; Li X; Wang XZ; Zhang M; Qu XK; Yang YQ
    Int J Mol Med; 2014 May; 33(5):1219-26. PubMed ID: 24638895
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus.
    Huang RT; Wang J; Xue S; Qiu XB; Shi HY; Li RG; Qu XK; Yang XX; Liu H; Li N; Li YJ; Xu YJ; Yang YQ
    Int J Med Sci; 2017; 14(4):323-332. PubMed ID: 28553164
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. PITX2 loss-of-function mutation contributes to tetralogy of Fallot.
    Sun YM; Wang J; Qiu XB; Yuan F; Xu YJ; Li RG; Qu XK; Huang RT; Xue S; Yang YQ
    Gene; 2016 Feb; 577(2):258-64. PubMed ID: 26657035
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot.
    Lu CX; Gong HR; Liu XY; Wang J; Zhao CM; Huang RT; Xue S; Yang YQ
    Int J Mol Med; 2016 Feb; 37(2):445-51. PubMed ID: 26676105
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel NKX2-5 mutations responsible for congenital heart disease.
    Wang J; Liu XY; Yang YQ
    Genet Mol Res; 2011 Nov; 10(4):2905-15. PubMed ID: 22179962
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart disease.
    Zhao L; Ni SH; Liu XY; Wei D; Yuan F; Xu L; Xin-Li ; Li RG; Qu XK; Xu YJ; Fang WY; Yang YQ; Qiu XB
    Eur J Med Genet; 2014 Oct; 57(10):579-86. PubMed ID: 25195019
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Compound heterozygous GATA5 mutations in a girl with hydrops fetalis, congenital heart defects and genital anomalies.
    Hempel M; Casar Tena T; Diehl T; Burczyk MS; Strom TM; Kubisch C; Philipp M; Lessel D
    Hum Genet; 2017 Mar; 136(3):339-346. PubMed ID: 28180938
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Functional polymorphisms of the neuropilin 1 gene are associated with the risk of tetralogy of Fallot in a Chinese Han population.
    Fan SH; Shen ZY; Xiao YM
    Gene; 2018 May; 653():72-79. PubMed ID: 29432830
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CpG site hypomethylation at ETS1‑binding region regulates DLK1 expression in Chinese patients with Tetralogy of Fallot.
    Tian G; He L; Gu R; Sun J; Chen W; Qian Y; Ma X; Yan W; Zhao Z; Xu Z; Suo M; Sheng W; Huang G
    Mol Med Rep; 2022 Mar; 25(3):. PubMed ID: 35059744
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.