BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 23626780)

  • 1. 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]  

  • 2. 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]  

  • 3. MEF2C loss-of-function mutation contributes to congenital heart defects.
    Qiao XH; Wang F; Zhang XL; Huang RT; Xue S; Wang J; Qiu XB; Liu XY; Yang YQ
    Int J Med Sci; 2017; 14(11):1143-1153. PubMed ID: 29104469
    [TBL] [Abstract][Full Text] [Related]  

  • 4. GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co-occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenital heart disease.
    Kalayinia S; Maleki M; Rokni-Zadeh H; Changi-Ashtiani M; Ahangar H; Biglari A; Shahani T; Mahdieh N
    J Clin Lab Anal; 2019 Sep; 33(7):e22923. PubMed ID: 31115957
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two novel missense mutations of GATA4 gene in Chinese patients with sporadic congenital heart defects.
    Tang ZH; Xia L; Chang W; Li H; Shen F; Liu JY; Wang Q; Liu MG
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Apr; 23(2):134-7. PubMed ID: 16604480
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [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]  

  • 8. 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]  

  • 9. 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]  

  • 10. A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease.
    Zhang X; Wang J; Wang B; Chen S; Fu Q; Sun K
    PLoS One; 2016; 11(7):e0158904. PubMed ID: 27391137
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Novel Point Mutations in 3'-Untranslated Region of GATA4 Gene Are Associated with Sporadic Non-syndromic Atrial and Ventricular Septal Defects.
    Khatami M; Ghorbani S; Adriani MR; Bahaloo S; Naeini MA; Heidari MM; Hadadzadeh M
    Curr Med Sci; 2022 Feb; 42(1):129-143. PubMed ID: 34652630
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. GATA4 mutations in 357 unrelated patients with congenital heart malformation.
    Butler TL; Esposito G; Blue GM; Cole AD; Costa MW; Waddell LB; Walizada G; Sholler GF; Kirk EP; Feneley M; Harvey RP; Winlaw DS
    Genet Test Mol Biomarkers; 2010 Dec; 14(6):797-802. PubMed ID: 20874241
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. A novel mutation in GATA4 gene associated with dominant inherited familial atrial septal defect.
    Chen Y; Han ZQ; Yan WD; Tang CZ; Xie JY; Chen H; Hu DY
    J Thorac Cardiovasc Surg; 2010 Sep; 140(3):684-7. PubMed ID: 20347099
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Screening and biochemical analysis of GATA4 sequence variations identified in patients with congenital heart disease.
    Schluterman MK; Krysiak AE; Kathiriya IS; Abate N; Chandalia M; Srivastava D; Garg V
    Am J Med Genet A; 2007 Apr; 143A(8):817-23. PubMed ID: 17352393
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.