151 related articles for article (PubMed ID: 25963046)
21. Synergistic activation of cardiac genes by myocardin and Tbx5.
Wang C; Cao D; Wang Q; Wang DZ
PLoS One; 2011; 6(8):e24242. PubMed ID: 21897873
[TBL] [Abstract][Full Text] [Related]
22. Transgenic analysis of the atrialnatriuretic factor (ANF) promoter: Nkx2-5 and GATA-4 binding sites are required for atrial specific expression of ANF.
Small EM; Krieg PA
Dev Biol; 2003 Sep; 261(1):116-31. PubMed ID: 12941624
[TBL] [Abstract][Full Text] [Related]
23. The complete sequence of mtDNA genes in idiopathic dilated cardiomyopathy shows novel missense and tRNA mutations.
Marin-Garcia J; Goldenthal MJ; Ananthakrishnan R; Pierpont ME
J Card Fail; 2000 Dec; 6(4):321-9. PubMed ID: 11145757
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Hey basic helix-loop-helix transcription factors are repressors of GATA4 and GATA6 and restrict expression of the GATA target gene ANF in fetal hearts.
Fischer A; Klattig J; Kneitz B; Diez H; Maier M; Holtmann B; Englert C; Gessler M
Mol Cell Biol; 2005 Oct; 25(20):8960-70. PubMed ID: 16199874
[TBL] [Abstract][Full Text] [Related]
26. GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.
Garg V; Kathiriya IS; Barnes R; Schluterman MK; King IN; Butler CA; Rothrock CR; Eapen RS; Hirayama-Yamada K; Joo K; Matsuoka R; Cohen JC; Srivastava D
Nature; 2003 Jul; 424(6947):443-7. PubMed ID: 12845333
[TBL] [Abstract][Full Text] [Related]
27. A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy.
Posch MG; Posch MJ; Geier C; Erdmann B; Mueller W; Richter A; Ruppert V; Pankuweit S; Maisch B; Perrot A; Buttgereit J; Dietz R; Haverkamp W; Ozcelik C
Mol Genet Metab; 2008; 95(1-2):74-80. PubMed ID: 18678517
[TBL] [Abstract][Full Text] [Related]
28. Identification of the TBX5 transactivating domain and the nuclear localization signal.
Zaragoza MV; Lewis LE; Sun G; Wang E; Li L; Said-Salman I; Feucht L; Huang T
Gene; 2004 Apr; 330():9-18. PubMed ID: 15087119
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding.
van de Meerakker JB; Christiaans I; Barnett P; Lekanne Deprez RH; Ilgun A; Mook OR; Mannens MM; Lam J; Wilde AA; Moorman AF; Postma AV
Biochim Biophys Acta; 2013 Apr; 1833(4):833-9. PubMed ID: 23147248
[TBL] [Abstract][Full Text] [Related]
31. Mutations in the dystrophin gene are associated with sporadic dilated cardiomyopathy.
Feng J; Yan J; Buzin CH; Towbin JA; Sommer SS
Mol Genet Metab; 2002; 77(1-2):119-26. PubMed ID: 12359139
[TBL] [Abstract][Full Text] [Related]
32. Evaluation of 10 genes encoding cardiac proteins in Doberman Pinschers with dilated cardiomyopathy.
O'Sullivan ML; O'Grady MR; Pyle WG; Dawson JF
Am J Vet Res; 2011 Jul; 72(7):932-9. PubMed ID: 21728854
[TBL] [Abstract][Full Text] [Related]
33. A novel GATA4 mutation responsible for congenital ventricular septal defects.
Wang J; Fang M; Liu XY; Xin YF; Liu ZM; Chen XZ; Wang XZ; Fang WY; Liu X; Yang YQ
Int J Mol Med; 2011 Oct; 28(4):557-64. PubMed ID: 21637914
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy.
Taylor MR; Slavov D; Gajewski A; Vlcek S; Ku L; Fain PR; Carniel E; Di Lenarda A; Sinagra G; Boucek MM; Cavanaugh J; Graw SL; Ruegg P; Feiger J; Zhu X; Ferguson DA; Bristow MR; Gotzmann J; Foisner R; Mestroni L;
Hum Mutat; 2005 Dec; 26(6):566-74. PubMed ID: 16247757
[TBL] [Abstract][Full Text] [Related]
36. A novel genetic variant in the transcription factor Islet-1 exerts gain of function on myocyte enhancer factor 2C promoter activity.
Friedrich FW; Dilanian G; Khattar P; Juhr D; Gueneau L; Charron P; Fressart V; Vilquin JT; Isnard R; Gouya L; Richard P; Hammoudi N; Komajda M; Bonne G; Eschenhagen T; Dubourg O; Villard E; Carrier L
Eur J Heart Fail; 2013 Mar; 15(3):267-76. PubMed ID: 23152444
[TBL] [Abstract][Full Text] [Related]
37. Identification of a missense mutation in the melusin-encoding ITGB1BP2 gene in a patient with dilated cardiomyopathy.
Ruppert V; Meyer T; Richter A; Maisch B; Pankuweit S;
Gene; 2013 Jan; 512(2):206-10. PubMed ID: 23124043
[TBL] [Abstract][Full Text] [Related]
38. Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathy.
Duboscq-Bidot L; Charron P; Ruppert V; Fauchier L; Richter A; Tavazzi L; Arbustini E; Wichter T; Maisch B; Komajda M; Isnard R; Villard E;
Eur Heart J; 2009 Sep; 30(17):2128-36. PubMed ID: 19525294
[TBL] [Abstract][Full Text] [Related]
39. Association of a G994-->T missense mutation in the plasma platelet-activating factor acetylhydrolase gene with genetic susceptibility to nonfamilial dilated cardiomyopathy in Japanese.
Ichihara S; Yamada Y; Yokota M
Circulation; 1998 Nov; 98(18):1881-5. PubMed ID: 9799208
[TBL] [Abstract][Full Text] [Related]
40. Interaction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac development.
Maitra M; Schluterman MK; Nichols HA; Richardson JA; Lo CW; Srivastava D; Garg V
Dev Biol; 2009 Feb; 326(2):368-77. PubMed ID: 19084512
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]