186 related articles for article (PubMed ID: 27391137)
21. Nuclear Receptor-Like Structure and Interaction of Congenital Heart Disease-Associated Factors GATA4 and NKX2-5.
Kinnunen S; Välimäki M; Tölli M; Wohlfahrt G; Darwich R; Komati H; Nemer M; Ruskoaho H
PLoS One; 2015; 10(12):e0144145. PubMed ID: 26642209
[TBL] [Abstract][Full Text] [Related]
22. Novel NKX2-5 mutations responsible for congenital heart disease.
Wang J; Liu XY; Yang YQ
Genet Mol Res; 2011 Nov; 10(4):2905-15. PubMed ID: 22179962
[TBL] [Abstract][Full Text] [Related]
23. A novel mutation of GATA4 (K319E) is responsible for familial atrial septal defect and pulmonary valve stenosis.
Xiang R; Fan LL; Huang H; Cao BB; Li XP; Peng DQ; Xia K
Gene; 2014 Jan; 534(2):320-3. PubMed ID: 24498650
[TBL] [Abstract][Full Text] [Related]
24. Functional analysis of the congenital heart disease‑associated GATA4 H436Y mutation in vitro.
Fang T; Zhu Y; Xu A; Zhang Y; Wu Q; Huang G; Sheng W; Chen M
Mol Med Rep; 2019 Sep; 20(3):2325-2331. PubMed ID: 31322241
[TBL] [Abstract][Full Text] [Related]
25. [Association of single nucleotide polymorphisms of transcription factors with congenital heart diseases in the Chinese population: a Meta analysis].
Chen LT; Yang TB; Wang TT; Zheng Z; Zhao LJ; Ye ZW; Zhang SM; Qin JB
Zhongguo Dang Dai Er Ke Za Zhi; 2018 Jun; 20(6):490-496. PubMed ID: 29972125
[TBL] [Abstract][Full Text] [Related]
26. A novel mutation of GATA4 in a familial atrial septal defect.
Chen Y; Mao J; Sun Y; Zhang Q; Cheng HB; Yan WH; Choy KW; Li H
Clin Chim Acta; 2010 Nov; 411(21-22):1741-5. PubMed ID: 20659440
[TBL] [Abstract][Full Text] [Related]
27. Congenital heart diseases and their association with the variant distribution features on susceptibility genes.
Su W; Zhu P; Wang R; Wu Q; Wang M; Zhang X; Mei L; Tang J; Kumar M; Wang X; Su L; Dong N
Clin Genet; 2017 Mar; 91(3):349-354. PubMed ID: 27426723
[TBL] [Abstract][Full Text] [Related]
28. Functional analysis of rare variants of GATA4 identified in Chinese patients with congenital heart defect.
Zhao Z; Zhan Y; Chen W; Ma X; Sheng W; Huang G
Genesis; 2019 Nov; 57(11-12):e23333. PubMed ID: 31513339
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. GATA4 mutations in 357 unrelated patients with congenital heart malformation.
Butler TL; Esposito G; Blue GM; Cole AD; Costa MW; Waddell LB; Walizada G; Sholler GF; Kirk EP; Feneley M; Harvey RP; Winlaw DS
Genet Test Mol Biomarkers; 2010 Dec; 14(6):797-802. PubMed ID: 20874241
[TBL] [Abstract][Full Text] [Related]
31. GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy.
Li RG; Li L; Qiu XB; Yuan F; Xu L; Li X; Xu YJ; Jiang WF; Jiang JQ; Liu X; Fang WY; Zhang M; Peng LY; Qu XK; Yang YQ
Biochem Biophys Res Commun; 2013 Oct; 439(4):591-6. PubMed ID: 24041700
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart disease.
Zhao L; Ni SH; Liu XY; Wei D; Yuan F; Xu L; Xin-Li ; Li RG; Qu XK; Xu YJ; Fang WY; Yang YQ; Qiu XB
Eur J Med Genet; 2014 Oct; 57(10):579-86. PubMed ID: 25195019
[TBL] [Abstract][Full Text] [Related]
34. Copy number variations in the GATA4, NKX2-5, TBX5, BMP4 CRELD1, and 22q11.2 gene regions in Chinese children with sporadic congenital heart disease.
Li Z; Huang J; Liang B; Zeng D; Luo S; Yan T; Liao F; Huang J; Li J; Cai R; Deng X; Tang N
J Clin Lab Anal; 2019 Feb; 33(2):e22660. PubMed ID: 30221396
[TBL] [Abstract][Full Text] [Related]
35. A novel mutation of GATA4 (K300T) associated with familial atrial septal defect.
Chen J; Qi B; Zhao J; Liu W; Duan R; Zhang M
Gene; 2016 Jan; 575(2 Pt 2):473-477. PubMed ID: 26376067
[TBL] [Abstract][Full Text] [Related]
36. A novel GATA4 loss-of-function mutation associated with congenital ventricular septal defect.
Yang YQ; Li L; Wang J; Liu XY; Chen XZ; Zhang W; Wang XZ; Jiang JQ; Liu X; Fang WY
Pediatr Cardiol; 2012 Apr; 33(4):539-46. PubMed ID: 22101736
[TBL] [Abstract][Full Text] [Related]
37. GATA4 mutations in 486 Chinese patients with congenital heart disease.
Zhang W; Li X; Shen A; Jiao W; Guan X; Li Z
Eur J Med Genet; 2008; 51(6):527-35. PubMed ID: 18672102
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. 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]
40. [Novel GATA4 mutations identified in patients with congenital heart disease].
Wang J; Hu DY; Li XM; Xin YF; Zhou H; Wang LJ; Wang LM; Xu WJ
Zhonghua Yi Xue Za Zhi; 2010 Mar; 90(10):667-71. PubMed ID: 20450724
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
