BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 34905512)

  • 1. Sequencing of a Chinese tetralogy of Fallot cohort reveals clustering mutations in myogenic heart progenitors.
    Tang CSM; Mononen M; Lam WY; Jin SC; Zhuang X; Garcia-Barcelo MM; Lin Q; Yang Y; Sahara M; Eroglu E; Chien KR; Hong H; Tam PKH; Gruber PJ
    JCI Insight; 2022 Jan; 7(2):. PubMed ID: 34905512
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Gene-environment regulatory circuits of right ventricular pathology in tetralogy of fallot.
    Zhao Y; Kang X; Gao F; Guzman A; Lau RP; Biniwale R; Wadehra M; Reemtsen B; Garg M; Halnon N; Quintero-Rivera F; Van Arsdell G; Coppola G; Nelson SF; Touma M;
    J Mol Med (Berl); 2019 Dec; 97(12):1711-1722. PubMed ID: 31834445
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.
    Page DJ; Miossec MJ; Williams SG; Monaghan RM; Fotiou E; Cordell HJ; Sutcliffe L; Topf A; Bourgey M; Bourque G; Eveleigh R; Dunwoodie SL; Winlaw DS; Bhattacharya S; Breckpot J; Devriendt K; Gewillig M; Brook JD; Setchfield KJ; Bu'Lock FA; O'Sullivan J; Stuart G; Bezzina CR; Mulder BJM; Postma AV; Bentham JR; Baron M; Bhaskar SS; Black GC; Newman WG; Hentges KE; Lathrop GM; Santibanez-Koref M; Keavney BD
    Circ Res; 2019 Feb; 124(4):553-563. PubMed ID: 30582441
    [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. 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]  

  • 6. Induced pluripotent stem cells of patients with Tetralogy of Fallot reveal transcriptional alterations in cardiomyocyte differentiation.
    Grunert M; Appelt S; Schönhals S; Mika K; Cui H; Cooper A; Cyganek L; Guan K; Sperling SR
    Sci Rep; 2020 Jul; 10(1):10921. PubMed ID: 32616843
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic variants at 10p11 confer risk of Tetralogy of Fallot in Chinese of Nanjing.
    Xu J; Lin Y; Si L; Jin G; Dai J; Wang C; Chen J; Da M; Hu Y; Yi C; Hu Z; Shen H; Mo X; Chen Y; Wang X
    PLoS One; 2014; 9(3):e89636. PubMed ID: 24594544
    [TBL] [Abstract][Full Text] [Related]  

  • 8. MicroRNA deregulation in right ventricular outflow tract myocardium in nonsyndromic tetralogy of fallot.
    Zhang J; Chang JJ; Xu F; Ma XJ; Wu Y; Li WC; Wang HJ; Huang GY; Ma D
    Can J Cardiol; 2013 Dec; 29(12):1695-703. PubMed ID: 24140236
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot.
    Reuter MS; Chaturvedi RR; Jobling RK; Pellecchia G; Hamdan O; Sung WWL; Nalpathamkalam T; Attaluri P; Silversides CK; Wald RM; Marshall CR; Williams SG; Keavney BD; Thiruvahindrapuram B; Scherer SW; Bassett AS
    Circ Genom Precis Med; 2021 Aug; 14(4):e003410. PubMed ID: 34328347
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.
    Greenway SC; Pereira AC; Lin JC; DePalma SR; Israel SJ; Mesquita SM; Ergul E; Conta JH; Korn JM; McCarroll SA; Gorham JM; Gabriel S; Altshuler DM; Quintanilla-Dieck Mde L; Artunduaga MA; Eavey RD; Plenge RM; Shadick NA; Weinblatt ME; De Jager PL; Hafler DA; Breitbart RE; Seidman JG; Seidman CE
    Nat Genet; 2009 Aug; 41(8):931-5. PubMed ID: 19597493
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Family-based whole-genome sequencing identifies compound heterozygous protein-coding and noncoding mutations in tetralogy of Fallot.
    Wang Y; Jiang T; Tang P; Wu Y; Jiang Z; Dai J; Gu Y; Xu J; Da M; Ma H; Jin G; Mo X; Li Q; Wang X; Hu Z
    Gene; 2020 May; 741():144555. PubMed ID: 32165302
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways.
    Silversides CK; Lionel AC; Costain G; Merico D; Migita O; Liu B; Yuen T; Rickaby J; Thiruvahindrapuram B; Marshall CR; Scherer SW; Bassett AS
    PLoS Genet; 2012; 8(8):e1002843. PubMed ID: 22912587
    [TBL] [Abstract][Full Text] [Related]  

  • 18. WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation.
    Hao L; Ma J; Wu F; Ma X; Qian M; Sheng W; Yan T; Tang N; Jiang X; Zhang B; Xiao D; Qian Y; Zhang J; Jiang N; Zhou W; Chen W; Ma D; Huang G
    Clin Transl Med; 2022 Jul; 12(7):e941. PubMed ID: 35808830
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseases.
    Grunert M; Dorn C; Cui H; Dunkel I; Schulz K; Schoenhals S; Sun W; Berger F; Chen W; Sperling SR
    Cardiovasc Res; 2016 Oct; 112(1):464-77. PubMed ID: 27496870
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Gene expression analysis in cardiac tissues from infants identifies candidate agents for Tetralogy of Fallot.
    Yang D; Li J; Yuan Z
    Pediatr Cardiol; 2013 Oct; 34(7):1637-44. PubMed ID: 23563574
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.