BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 32236096)

  • 1. TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway.
    Miyao N; Hata Y; Izumi H; Nagaoka R; Oku Y; Takasaki I; Ishikawa T; Takarada S; Okabe M; Nakaoka H; Ibuki K; Ozawa S; Yoshida T; Hasegawa H; Makita N; Nishida N; Mori H; Ichida F; Hirono K
    PLoS One; 2020; 15(4):e0227393. PubMed ID: 32236096
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel TBX5 loss-of-function mutation associated with sporadic dilated cardiomyopathy.
    Zhou W; Zhao L; Jiang JQ; Jiang WF; Yang YQ; Qiu XB
    Int J Mol Med; 2015 Jul; 36(1):282-8. PubMed ID: 25963046
    [TBL] [Abstract][Full Text] [Related]  

  • 3. KLF13 is a genetic modifier of the Holt-Oram syndrome gene TBX5.
    Darwich R; Li W; Yamak A; Komati H; Andelfinger G; Sun K; Nemer M
    Hum Mol Genet; 2017 Mar; 26(5):942-954. PubMed ID: 28164238
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel de novo CASZ1 heterozygous frameshift variant causes dilated cardiomyopathy and left ventricular noncompaction cardiomyopathy.
    Guo J; Li Z; Hao C; Guo R; Hu X; Qian S; Zeng J; Gao H; Li W
    Mol Genet Genomic Med; 2019 Aug; 7(8):e828. PubMed ID: 31268246
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy.
    Zhang XL; Qiu XB; Yuan F; Wang J; Zhao CM; Li RG; Xu L; Xu YJ; Shi HY; Hou XM; Qu XK; Xu YW; Yang YQ
    Biochem Biophys Res Commun; 2015 Mar; 459(1):166-71. PubMed ID: 25725155
    [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. Incidental diagnosis of a familial left ventricular noncompaction on a chest CT angiography.
    Dubourg B; D'Heré B; de Vecchi C; Caudron J; Savoure A; Stepowski D; Lefebvre V; Bauer F; Eltchaninoff H; Dacher JN
    Diagn Interv Imaging; 2014 Jan; 95(1):91-3. PubMed ID: 24018053
    [No Abstract]   [Full Text] [Related]  

  • 9. Tbx5 specifies the left/right ventricles and ventricular septum position during cardiogenesis.
    Takeuchi JK; Ohgi M; Koshiba-Takeuchi K; Shiratori H; Sakaki I; Ogura K; Saijoh Y; Ogura T
    Development; 2003 Dec; 130(24):5953-64. PubMed ID: 14573514
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Tbx5 and Osr1 interact to regulate posterior second heart field cell cycle progression for cardiac septation.
    Zhou L; Liu J; Olson P; Zhang K; Wynne J; Xie L
    J Mol Cell Cardiol; 2015 Aug; 85():1-12. PubMed ID: 25986147
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Left ventricle non-compaction: The still misdiagnosed cardiomyopathy.
    Lorca R; Martín M; Reguero JJR; Díaz-Molina B; Morís C; Lambert JL; Astudillo A
    Int J Cardiol; 2016 Nov; 223():420-421. PubMed ID: 27544597
    [No Abstract]   [Full Text] [Related]  

  • 12. Preclinical evidence for the therapeutic value of TBX5 normalization in arrhythmia control.
    Rathjens FS; Blenkle A; Iyer LM; Renger A; Syeda F; Noack C; Jungmann A; Dewenter M; Toischer K; El-Armouche A; Müller OJ; Fabritz L; Zimmermann WH; Zelarayan LC; Zafeiriou MP
    Cardiovasc Res; 2021 Jul; 117(8):1908-1922. PubMed ID: 32777030
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease.
    Bruneau BG; Nemer G; Schmitt JP; Charron F; Robitaille L; Caron S; Conner DA; Gessler M; Nemer M; Seidman CE; Seidman JG
    Cell; 2001 Sep; 106(6):709-21. PubMed ID: 11572777
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A New TBX5 Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular Block.
    Zhang Y; Sun YM; Xu YJ; Zhao CM; Yuan F; Guo XJ; Guo YH; Yang CX; Gu JN; Qiao Q; Wang J; Yang YQ
    Int Heart J; 2020 Jul; 61(4):761-768. PubMed ID: 32641638
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Disruption of myocardial Gata4 and Tbx5 results in defects in cardiomyocyte proliferation and atrioventricular septation.
    Misra C; Chang SW; Basu M; Huang N; Garg V
    Hum Mol Genet; 2014 Oct; 23(19):5025-35. PubMed ID: 24858909
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exome Sequencing Identifies Pathogenic and Modifier Mutations in a Child With Sporadic Dilated Cardiomyopathy.
    Long PA; Larsen BT; Evans JM; Olson TM
    J Am Heart Assoc; 2015 Dec; 4(12):. PubMed ID: 26656454
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CHF1/Hey2 plays a pivotal role in left ventricular maturation through suppression of ectopic atrial gene expression.
    Koibuchi N; Chin MT
    Circ Res; 2007 Mar; 100(6):850-5. PubMed ID: 17332425
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. The Desmin (
    Kulikova O; Brodehl A; Kiseleva A; Myasnikov R; Meshkov A; Stanasiuk C; Gärtner A; Divashuk M; Sotnikova E; Koretskiy S; Kharlap M; Kozlova V; Mershina E; Pilus P; Sinitsyn V; Milting H; Boytsov S; Drapkina O
    Genes (Basel); 2021 Jan; 12(1):. PubMed ID: 33478057
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A gain-of-function TBX5 mutation is associated with atypical Holt-Oram syndrome and paroxysmal atrial fibrillation.
    Postma AV; van de Meerakker JB; Mathijssen IB; Barnett P; Christoffels VM; Ilgun A; Lam J; Wilde AA; Lekanne Deprez RH; Moorman AF
    Circ Res; 2008 Jun; 102(11):1433-42. PubMed ID: 18451335
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.