281 related articles for article (PubMed ID: 24000169)
21. A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect.
Lin X; Huo Z; Liu X; Zhang Y; Li L; Zhao H; Yan B; Liu Y; Yang Y; Chen YH
J Hum Genet; 2010 Oct; 55(10):662-7. PubMed ID: 20631719
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot.
El Bouchikhi I; Belhassan K; Moufid FZ; Houssaini MI; Bouguenouch L; Samri I; Bouhrim M; Ouldim K; Atmani S
Afr Health Sci; 2018 Dec; 18(4):922-930. PubMed ID: 30766556
[TBL] [Abstract][Full Text] [Related]
24. Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot.
Pizzuti A; Sarkozy A; Newton AL; Conti E; Flex E; Digilio MC; Amati F; Gianni D; Tandoi C; Marino B; Crossley M; Dallapiccola B
Hum Mutat; 2003 Nov; 22(5):372-7. PubMed ID: 14517948
[TBL] [Abstract][Full Text] [Related]
25. Prevalence and spectrum of GATA4 mutations associated with sporadic dilated cardiomyopathy.
Li J; Liu WD; Yang ZL; Yuan F; Xu L; Li RG; Yang YQ
Gene; 2014 Sep; 548(2):174-81. PubMed ID: 25017055
[TBL] [Abstract][Full Text] [Related]
26. Somatic GATA5 mutations in sporadic tetralogy of Fallot.
Huang RT; Xue S; Xu YJ; Zhou M; Yang YQ
Int J Mol Med; 2014 May; 33(5):1227-35. PubMed ID: 24573614
[TBL] [Abstract][Full Text] [Related]
27. GATA4 loss-of-function mutations in familial atrial fibrillation.
Yang YQ; Wang MY; Zhang XL; Tan HW; Shi HF; Jiang WF; Wang XH; Fang WY; Liu X
Clin Chim Acta; 2011 Sep; 412(19-20):1825-30. PubMed ID: 21708142
[TBL] [Abstract][Full Text] [Related]
28. Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.
LaHaye S; Corsmeier D; Basu M; Bowman JL; Fitzgerald-Butt S; Zender G; Bosse K; McBride KL; White P; Garg V
Circ Cardiovasc Genet; 2016 Aug; 9(4):320-9. PubMed ID: 27418595
[TBL] [Abstract][Full Text] [Related]
29. Novel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of fallot.
Wang J; Luo XJ; Xin YF; Liu Y; Liu ZM; Wang Q; Li RG; Fang WY; Wang XZ; Yang YQ
DNA Cell Biol; 2012 Nov; 31(11):1610-7. PubMed ID: 23020118
[TBL] [Abstract][Full Text] [Related]
30. 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]
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. 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]
33. TBX20 loss-of-function mutation associated with familial dilated cardiomyopathy.
Zhao CM; Bing-Sun ; Song HM; Wang J; Xu WJ; Jiang JF; Qiu XB; Yuan F; Xu JH; Yang YQ
Clin Chem Lab Med; 2016 Feb; 54(2):325-32. PubMed ID: 26118961
[TBL] [Abstract][Full Text] [Related]
34. Mutations in the cardiac transcription factor GATA4 in patients with lone atrial fibrillation.
Posch MG; Boldt LH; Polotzki M; Richter S; Rolf S; Perrot A; Dietz R; Ozcelik C; Haverkamp W
Eur J Med Genet; 2010; 53(4):201-3. PubMed ID: 20363377
[TBL] [Abstract][Full Text] [Related]
35. A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.
Sun YM; Wang J; Qiu XB; Yuan F; Li RG; Xu YJ; Qu XK; Shi HY; Hou XM; Huang RT; Xue S; Yang YQ
G3 (Bethesda); 2016 Apr; 6(4):987-92. PubMed ID: 26865696
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. The effect of human GATA4 gene mutations on the activity of target gonadal promoters.
Bouchard MF; Taniguchi H; Viger RS
J Mol Endocrinol; 2009 Feb; 42(2):149-60. PubMed ID: 19008335
[TBL] [Abstract][Full Text] [Related]
39. [Novel GATA4 mutations identified in patients with congenital atrial septal defects].
Liu XY; Yang YQ; Ma J; Lin XP; Zheng JH; Bai K; Chen YH
Zhonghua Xin Xue Guan Bing Za Zhi; 2010 Aug; 38(8):724-7. PubMed ID: 21055141
[TBL] [Abstract][Full Text] [Related]
40. GATA5 loss-of-function mutation in familial dilated cardiomyopathy.
Zhang XL; Dai N; Tang K; Chen YQ; Chen W; Wang J; Zhao CM; Yuan F; Qiu XB; Qu XK; Yang YQ; Xu YW
Int J Mol Med; 2015 Mar; 35(3):763-70. PubMed ID: 25543888
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]