BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

212 related articles for article (PubMed ID: 31386585)

  • 1. The Functional Polymorphism R129W in the
    Shi Y; Li Y; Wang Y; Zhuang J; Wang H; Hu M; Mo X; Yue S; Chen Y; Fan X; Chen J; Cai W; Zhu X; Wan Y; Zhong Y; Ye X; Li F; Zhou Z; Dai G; Luo R; Ocorr K; Jiang Z; Li X; Zhu P; Wu X; Yuan W
    Genet Test Mol Biomarkers; 2019 Sep; 23(9):601-609. PubMed ID: 31386585
    [No Abstract]   [Full Text] [Related]  

  • 2. BVES downregulation in non-syndromic tetralogy of fallot is associated with ventricular outflow tract stenosis.
    Shi Y; Li Y; Wang Y; Zhu P; Chen Y; Wang H; Yue S; Xia X; Chen J; Jiang Z; Zhou C; Cai W; Yuan H; Wu Y; Wan Y; Li X; Zhu X; Zhou Z; Dai G; Li F; Mo X; Ye X; Fan X; Zhuang J; Wu X; Yuan W
    Sci Rep; 2020 Aug; 10(1):14167. PubMed ID: 32843646
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutational and functional analysis of the BVES gene coding region in Chinese patients with non-syndromic tetralogy of Fallot.
    Wu M; Li Y; He X; Shao X; Yang F; Zhao M; Wu C; Zhang C; Zhou L
    Int J Mol Med; 2013 Apr; 31(4):899-903. PubMed ID: 23403794
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Genetic variations of VEGF gene were associated with tetralogy of fallot risk in a Chinese Han population.
    Yan L; Ge Q; Xi C; Zhang X; Guo Y
    Genet Test Mol Biomarkers; 2015 May; 19(5):264-71. PubMed ID: 25894981
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Functionally significant, novel GATA4 variants are frequently associated with Tetralogy of Fallot.
    Dixit R; Narasimhan C; Balekundri VI; Agrawal D; Kumar A; Mohapatra B
    Hum Mutat; 2018 Dec; 39(12):1957-1972. PubMed ID: 30152191
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Investigation of somatic NKX2-5, GATA4 and HAND1 mutations in patients with tetralogy of Fallot.
    Wang J; Lu Y; Chen H; Yin M; Yu T; Fu Q
    Pathology; 2011 Jun; 43(4):322-6. PubMed ID: 21519287
    [TBL] [Abstract][Full Text] [Related]  

  • 8. DNA methylation status of NKX2-5, GATA4 and HAND1 in patients with tetralogy of fallot.
    Sheng W; Qian Y; Wang H; Ma X; Zhang P; Diao L; An Q; Chen L; Ma D; Huang G
    BMC Med Genomics; 2013 Nov; 6():46. PubMed ID: 24182332
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Somatic mutations in NKX2–5, GATA4, and HAND1 are not a common cause of tetralogy of Fallot or hypoplastic left heart.
    Esposito G; Butler TL; Blue GM; Cole AD; Sholler GF; Kirk EP; Grossfeld P; Perryman BM; Harvey RP; Winlaw DS
    Am J Med Genet A; 2011 Oct; 155A(10):2416-21. PubMed ID: 22043484
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Intronic Polymorphisms in Gene of Second Heart Field as Risk Factors for Human Congenital Heart Disease in a Chinese Population.
    Wang E; Nie Y; Fan X; Zheng Z; Hu S
    DNA Cell Biol; 2019 Jun; 38(6):521-531. PubMed ID: 31013439
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications.
    He GW; Maslen CL; Chen HX; Hou HT; Bai XY; Wang XL; Liu XC; Lu WL; Chen XX; Chen WD; Xing QS; Wu Q; Wang J; Yang Q
    Clin Genet; 2022 Nov; 102(5):391-403. PubMed ID: 35882632
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Functionally significant, rare transcription factor variants in tetralogy of Fallot.
    Töpf A; Griffin HR; Glen E; Soemedi R; Brown DL; Hall D; Rahman TJ; Eloranta JJ; Jüngst C; Stuart AG; O'Sullivan J; Keavney BD; Goodship JA
    PLoS One; 2014; 9(8):e95453. PubMed ID: 25093829
    [TBL] [Abstract][Full Text] [Related]  

  • 18. VEGF Gene Polymorphisms are Associated with Risk of Tetralogy of Fallot.
    Li X; Liu CL; Li XX; Li QC; Ma LM; Liu GL
    Med Sci Monit; 2015 Nov; 21():3474-82. PubMed ID: 26558525
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Single nucleotide polymorphism of NKX2-5 gene with sporadic congenital heart disease in Chinese Bai population.
    Cao Y; Lan W; Li Y; Wei C; Zou H; Jiang L
    Int J Clin Exp Pathol; 2015; 8(11):14917-24. PubMed ID: 26823822
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot.
    Goodship JA; Hall D; Topf A; Mamasoula C; Griffin H; Rahman TJ; Glen E; Tan H; Palomino Doza J; Relton CL; Bentham J; Bhattacharya S; Cosgrove C; Brook D; Granados-Riveron J; Bu'Lock FA; O'Sullivan J; Stuart AG; Parsons J; Cordell HJ; Keavney B
    Circ Cardiovasc Genet; 2012 Jun; 5(3):287-92. PubMed ID: 22503907
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.