BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

272 related articles for article (PubMed ID: 18672102)

  • 1. GATA4 mutations in 486 Chinese patients with congenital heart disease.
    Zhang W; Li X; Shen A; Jiao W; Guan X; Li Z
    Eur J Med Genet; 2008; 51(6):527-35. PubMed ID: 18672102
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Novel GATA4 mutations identified in patients with congenital heart disease].
    Wang J; Hu DY; Li XM; Xin YF; Zhou H; Wang LJ; Wang LM; Xu WJ
    Zhonghua Yi Xue Za Zhi; 2010 Mar; 90(10):667-71. PubMed ID: 20450724
    [TBL] [Abstract][Full Text] [Related]  

  • 3. T-box transcription factor TBX20 mutations in Chinese patients with congenital heart disease.
    Liu C; Shen A; Li X; Jiao W; Zhang X; Li Z
    Eur J Med Genet; 2008; 51(6):580-7. PubMed ID: 18834961
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD).
    Reamon-Buettner SM; Cho SH; Borlak J
    BMC Med Genet; 2007 Jun; 8():38. PubMed ID: 17592645
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease.
    Xiong F; Li Q; Zhang C; Chen Y; Li P; Wei X; Li Q; Zhou W; Li L; Shang X; Xu X
    Cardiovasc Pathol; 2013; 22(2):141-5. PubMed ID: 22959235
    [TBL] [Abstract][Full Text] [Related]  

  • 6. GATA4 and NKX2.5 gene analysis in Chinese Uygur patients with congenital heart disease.
    Zhang WM; Li XF; Ma ZY; Zhang J; Zhou SH; Li T; Shi L; Li ZZ
    Chin Med J (Engl); 2009 Feb; 122(4):416-9. PubMed ID: 19302747
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic analysis of the promoter region of the GATA4 gene in patients with ventricular septal defects.
    Wu G; Shan J; Pang S; Wei X; Zhang H; Yan B
    Transl Res; 2012 May; 159(5):376-82. PubMed ID: 22500510
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of functional mutations in GATA4 in patients with congenital heart disease.
    Wang E; Sun S; Qiao B; Duan W; Huang G; An Y; Xu S; Zheng Y; Su Z; Gu X; Jin L; Wang H
    PLoS One; 2013; 8(4):e62138. PubMed ID: 23626780
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Screening of 99 Danish patients with congenital heart disease for GATA4 mutations.
    Zhang L; Tümer Z; Jacobsen JR; Andersen PS; Tommerup N; Larsen LA
    Genet Test; 2006; 10(4):277-80. PubMed ID: 17253934
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Genetic screening for novel GATA4 mutations associated with congenital atrial septal defect].
    Wang J; Li XM; Xin YF; Wang LJ; Xu WJ; Hu DY
    Zhonghua Xin Xue Guan Bing Za Zhi; 2010 May; 38(5):429-34. PubMed ID: 20654103
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [Novel GATA4 mutations identified in patients with congenital atrial septal defects].
    Liu XY; Yang YQ; Ma J; Lin XP; Zheng JH; Bai K; Chen YH
    Zhonghua Xin Xue Guan Bing Za Zhi; 2010 Aug; 38(8):724-7. PubMed ID: 21055141
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects.
    Hamanoue H; Rahayuningsih SE; Hirahara Y; Itoh J; Yokoyama U; Mizuguchi T; Saitsu H; Miyake N; Hirahara F; Matsumoto N
    Cardiol Young; 2009 Sep; 19(5):482-5. PubMed ID: 19678963
    [TBL] [Abstract][Full Text] [Related]  

  • 15. c.620C>T mutation in GATA4 is associated with congenital heart disease in South India.
    Mattapally S; Nizamuddin S; Murthy KS; Thangaraj K; Banerjee SK
    BMC Med Genet; 2015 Feb; 16():7. PubMed ID: 25928801
    [TBL] [Abstract][Full Text] [Related]  

  • 16. GATA4 sequence variants in patients with congenital heart disease.
    Tomita-Mitchell A; Maslen CL; Morris CD; Garg V; Goldmuntz E
    J Med Genet; 2007 Dec; 44(12):779-83. PubMed ID: 18055909
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot.
    Nemer G; Fadlalah F; Usta J; Nemer M; Dbaibo G; Obeid M; Bitar F
    Hum Mutat; 2006 Mar; 27(3):293-4. PubMed ID: 16470721
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children.
    Behiry EG; Al-Azzouny MA; Sabry D; Behairy OG; Salem NE
    Mol Genet Genomic Med; 2019 May; 7(5):e612. PubMed ID: 30834692
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle.
    De Luca A; Sarkozy A; Ferese R; Consoli F; Lepri F; Dentici ML; Vergara P; De Zorzi A; Versacci P; Digilio MC; Marino B; Dallapiccola B
    Clin Genet; 2011 Aug; 80(2):184-90. PubMed ID: 20807224
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations in the perforin gene in children with hemophagocytic lymphohistiocytosis.
    Lu G; Xie ZD; Shen KL; Ye LJ; Wu RH; Liu CY; Jin YK; Yang S
    Chin Med J (Engl); 2009 Dec; 122(23):2851-5. PubMed ID: 20092789
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.