BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 25834824)

  • 1. Novel mutations in the transcriptional activator domain of the human TBX20 in patients with atrial septal defect.
    Monroy-Muñoz IE; Pérez-Hernández N; Rodríguez-Pérez JM; Muñoz-Medina JE; Angeles-Martínez J; García-Trejo JJ; Morales-Ríos E; Massó F; Sandoval-Jones JP; Cervantes-Salazar J; García-Montes JA; Calderón-Colmenero J; Vargas-Alarcón G
    Biomed Res Int; 2015; 2015():718786. PubMed ID: 25834824
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect.
    Liu JJ; Fan LL; Chen JL; Tan ZP; Yang YF
    J Zhejiang Univ Sci B; 2014 Sep; 15(9):830-7. PubMed ID: 25183037
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel TBX20 loss‑of‑function mutation contributes to adult‑onset dilated cardiomyopathy or congenital atrial septal defect.
    Zhou YM; Dai XY; Huang RT; Xue S; Xu YJ; Qiu XB; Yang YQ
    Mol Med Rep; 2016 Oct; 14(4):3307-14. PubMed ID: 27510170
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects.
    Posch MG; Gramlich M; Sunde M; Schmitt KR; Lee SH; Richter S; Kersten A; Perrot A; Panek AN; Al Khatib IH; Nemer G; Mégarbané A; Dietz R; Stiller B; Berger F; Harvey RP; Ozcelik C
    J Med Genet; 2010 Apr; 47(4):230-5. PubMed ID: 19762328
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic analysis of the TBX20 gene promoter region in patients with ventricular septal defects.
    Qiao Y; Wanyan H; Xing Q; Xie W; Pang S; Shan J; Yan B
    Gene; 2012 May; 500(1):28-31. PubMed ID: 22465533
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy.
    Kirk EP; Sunde M; Costa MW; Rankin SA; Wolstein O; Castro ML; Butler TL; Hyun C; Guo G; Otway R; Mackay JP; Waddell LB; Cole AD; Hayward C; Keogh A; Macdonald P; Griffiths L; Fatkin D; Sholler GF; Zorn AM; Feneley MP; Winlaw DS; Harvey RP
    Am J Hum Genet; 2007 Aug; 81(2):280-91. PubMed ID: 17668378
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Association between Tbx20 gene polymorphism and congenital atrial septal defects].
    Ma Y; Xiang Y; Li X; Yang Y; Ma Y; Xie X; Liu F
    Zhonghua Nei Ke Za Zhi; 2015 Oct; 54(10):860-4. PubMed ID: 26675025
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial cardiac septal defect due to a novel nine-base deletion in TBX20.
    Yamamoto H; Inagaki H; Hayano S; Kurahashi H; Kato T
    Pediatr Int; 2022 Jan; 64(1):e14995. PubMed ID: 35298876
    [No Abstract]   [Full Text] [Related]  

  • 10. TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts.
    Reamon-Buettner SM; Borlak J
    Hum Mutat; 2004 Jul; 24(1):104. PubMed ID: 15221798
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of a novel and functional mutation in the TBX5 gene in a patient by screening from 354 patients with isolated ventricular septal defect.
    Chen HX; Zhang X; Hou HT; Wang J; Yang Q; Wang XL; He GW
    Eur J Med Genet; 2017 Jul; 60(7):385-390. PubMed ID: 28434921
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Involvement of a novel GATA4 mutation in atrial septal defects.
    Liu XY; Wang J; Zheng JH; Bai K; Liu ZM; Wang XZ; Liu X; Fang WY; Yang YQ
    Int J Mol Med; 2011 Jul; 28(1):17-23. PubMed ID: 21373748
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel TBX5 missense mutation (V263M) in a family with atrial septal defects and postaxial hexodactyly.
    Faria MH; Rabenhorst SH; Pereira AC; Krieger JE
    Int J Cardiol; 2008 Oct; 130(1):30-5. PubMed ID: 18706711
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Screening and evaluation of TBX20 and CITED2 mutations in children with congenital cardiac septal defects: Correlation with cardiac troponin T and caspase-3.
    Taha M; Awny N; Ismail S; Ashaat EA; Senousy MA
    Gene; 2023 Oct; 882():147660. PubMed ID: 37481008
    [TBL] [Abstract][Full Text] [Related]  

  • 15. TBX20 loss-of-function mutation contributes to double outlet right ventricle.
    Pan Y; Geng R; Zhou N; Zheng GF; Zhao H; Wang J; Zhao CM; Qiu XB; Yang YQ; Liu XY
    Int J Mol Med; 2015 Apr; 35(4):1058-66. PubMed ID: 25625280
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Association between the SNPs of human Tbx20 gene and congenital atrial septal defects in Uygur population of Xinjiang region].
    Ma Y; Li X; Yang Y; Ma Y; Xie X; Li H; Liu F
    Zhonghua Liu Xing Bing Xue Za Zhi; 2014 Jul; 35(7):872-3. PubMed ID: 25326924
    [No Abstract]   [Full Text] [Related]  

  • 17. Mutation in myosin heavy chain 6 causes atrial septal defect.
    Ching YH; Ghosh TK; Cross SJ; Packham EA; Honeyman L; Loughna S; Robinson TE; Dearlove AM; Ribas G; Bonser AJ; Thomas NR; Scotter AJ; Caves LS; Tyrrell GP; Newbury-Ecob RA; Munnich A; Bonnet D; Brook JD
    Nat Genet; 2005 Apr; 37(4):423-8. PubMed ID: 15735645
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular basis of the clinical features of Holt-Oram syndrome resulting from missense and extended protein mutations of the TBX5 gene as well as TBX5 intragenic duplications.
    Al-Qattan MM; Abou Al-Shaar H
    Gene; 2015 Apr; 560(2):129-36. PubMed ID: 25680289
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. Mutations in mammalian tolloid-like 1 gene detected in adult patients with ASD.
    Stańczak P; Witecka J; Szydło A; Gutmajster E; Lisik M; Auguściak-Duma A; Tarnowski M; Czekaj T; Czekaj H; Sieroń AL
    Eur J Hum Genet; 2009 Mar; 17(3):344-51. PubMed ID: 18830233
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.