247 related articles for article (PubMed ID: 30121862)
21. A novel mutation in GATA4 gene associated with dominant inherited familial atrial septal defect.
Chen Y; Han ZQ; Yan WD; Tang CZ; Xie JY; Chen H; Hu DY
J Thorac Cardiovasc Surg; 2010 Sep; 140(3):684-7. PubMed ID: 20347099
[TBL] [Abstract][Full Text] [Related]
22. TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus.
Huang RT; Wang J; Xue S; Qiu XB; Shi HY; Li RG; Qu XK; Yang XX; Liu H; Li N; Li YJ; Xu YJ; Yang YQ
Int J Med Sci; 2017; 14(4):323-332. PubMed ID: 28553164
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. Association of functional variant in GDF1 promoter with risk of congenital heart disease and its regulation by Nkx2.5.
Gao X; Zheng P; Yang L; Luo H; Zhang C; Qiu Y; Huang G; Sheng W; Ma X; Lu C
Clin Sci (Lond); 2019 Jun; 133(12):1281-1295. PubMed ID: 31171573
[TBL] [Abstract][Full Text] [Related]
26. Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations.
Reamon-Buettner SM; Hecker H; Spanel-Borowski K; Craatz S; Kuenzel E; Borlak J
Am J Pathol; 2004 Jun; 164(6):2117-25. PubMed ID: 15161646
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Genetic analysis of essential cardiac transcription factors in 256 patients with non-syndromic congenital heart defects.
Kodo K; Nishizawa T; Furutani M; Arai S; Ishihara K; Oda M; Makino S; Fukuda K; Takahashi T; Matsuoka R; Nakanishi T; Yamagishi H
Circ J; 2012; 76(7):1703-11. PubMed ID: 22498567
[TBL] [Abstract][Full Text] [Related]
29. Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy.
Xu JH; Gu JY; Guo YH; Zhang H; Qiu XB; Li RG; Shi HY; Liu H; Yang XX; Xu YJ; Qu XK; Yang YQ
Int Heart J; 2017 Aug; 58(4):521-529. PubMed ID: 28690296
[TBL] [Abstract][Full Text] [Related]
30. Investigation of NKX2.5 gene mutations in congenital heart defects in an Indian population.
Ketharnathan S; Koshy T; Sethuratnam R; Paul S; Venkatesan V
Genet Test Mol Biomarkers; 2015 Oct; 19(10):579-83. PubMed ID: 26273787
[TBL] [Abstract][Full Text] [Related]
31. Analysis of NKX2-5 in 439 Chinese Patients with Sporadic Atrial Septal Defect.
Wang H; Liu Y; Li Y; Wang W; Li L; Meng M; Xie Y; Zhang Y; Yunfeng Z; Han S; Zeng J; Hou Z; Jiang L
Med Sci Monit; 2019 Apr; 25():2756-2763. PubMed ID: 30982828
[TBL] [Abstract][Full Text] [Related]
32. Association between congenital heart disease and
González-Castro TB; Tovilla-Zárate CA; López-Narvaez ML; Juárez-Rojop IE; Calderón-Colmenero J; Sandoval JP; García-Montes JA; Blachman-Braun R; Castillo-Avila RG; García-Flores E; Cazarín-Santos BG; Borgonio-Cuadra VM; Posadas-Sánchez R; Vargas-Alarcón G; Rodríguez-Pérez JM; Pérez-Hernández N
Biomark Med; 2020 Dec; 14(18):1747-1757. PubMed ID: 33346701
[No Abstract] [Full Text] [Related]
33. 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]
34. Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease.
Stallmeyer B; Fenge H; Nowak-Göttl U; Schulze-Bahr E
Clin Genet; 2010 Dec; 78(6):533-40. PubMed ID: 20456451
[TBL] [Abstract][Full Text] [Related]
35. Germline mutations in NKX2-5, GATA4, and CRELD1 are rare in a Mexican sample of Down syndrome patients with endocardial cushion and septal heart defects.
Alcántara-Ortigoza MA; De Rubens-Figueroa J; Reyna-Fabian ME; Estandía-Ortega B; González-del Angel A; Molina-Álvarez B; Velázquez-Aragón JA; Villagómez-Martínez S; Pereira-López GI; Martínez-Cruz V; Álvarez-Gómez RM; Díaz-García L
Pediatr Cardiol; 2015 Apr; 36(4):802-8. PubMed ID: 25524324
[TBL] [Abstract][Full Text] [Related]
36. Two novel missense mutations of GATA4 gene in Chinese patients with sporadic congenital heart defects.
Tang ZH; Xia L; Chang W; Li H; Shen F; Liu JY; Wang Q; Liu MG
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Apr; 23(2):134-7. PubMed ID: 16604480
[TBL] [Abstract][Full Text] [Related]
37. Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD).
Reamon-Buettner SM; Cho SH; Borlak J
BMC Med Genet; 2007 Jun; 8():38. PubMed ID: 17592645
[TBL] [Abstract][Full Text] [Related]
38. Screening NKX2.5 mutation in a sample of 230 Han Chinese children with congenital heart diseases.
Zhang W; Li X; Shen A; Jiao W; Guan X; Li Z
Genet Test Mol Biomarkers; 2009 Apr; 13(2):159-62. PubMed ID: 19371212
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Genetic variations of NKX2-5 in sporadic atrial septal defect and ventricular septal defect in Chinese Yunnan population.
Cao Y; Wang J; Wei C; Hou Z; Li Y; Zou H; Meng M; Wang W; Jiang L
Gene; 2016 Jan; 575(1):29-33. PubMed ID: 26297999
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
