245 related articles for article (PubMed ID: 25742962)
21. [Mutation of NKX2-5 gene in patients with atrial septal defect].
Liu XY; Yang YQ; Yang Y; Lin XP; Chen YH
Zhonghua Er Ke Za Zhi; 2009 Sep; 47(9):696-700. PubMed ID: 20021795
[TBL] [Abstract][Full Text] [Related]
22. Novel NKX2-5 mutations in patients with familial atrial septal defects.
Liu XY; Wang J; Yang YQ; Zhang YY; Chen XZ; Zhang W; Wang XZ; Zheng JH; Chen YH
Pediatr Cardiol; 2011 Feb; 32(2):193-201. PubMed ID: 21188375
[TBL] [Abstract][Full Text] [Related]
23. Novel point mutation in the cardiac transcription factor CSX/NKX2.5 associated with congenital heart disease.
Ikeda Y; Hiroi Y; Hosoda T; Utsunomiya T; Matsuo S; Ito T; Inoue J; Sumiyoshi T; Takano H; Nagai R; Komuro I
Circ J; 2002 Jun; 66(6):561-3. PubMed ID: 12074273
[TBL] [Abstract][Full Text] [Related]
24. NKX2-6 related congenital heart disease: Biallelic homeodomain-disrupting variants and truncus arteriosus.
Ritter A; Werner P; Latney B; Krock BL; Santani A; Bedoukian E; Skraban CM; Deardorff MA; Goldmuntz E
Am J Med Genet A; 2020 Jun; 182(6):1454-1459. PubMed ID: 32198970
[TBL] [Abstract][Full Text] [Related]
25. Clinical and molecular characterisation of Holt-Oram syndrome focusing on cardiac manifestations.
Jhang WK; Lee BH; Kim GH; Lee JO; Yoo HW
Cardiol Young; 2015 Aug; 25(6):1093-8. PubMed ID: 25216260
[TBL] [Abstract][Full Text] [Related]
26. Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block.
Xu YJ; Qiu XB; Yuan F; Shi HY; Xu L; Hou XM; Qu XK; Liu X; Huang RT; Xue S; Yang YQ; Li RG
Mol Med Rep; 2017 Apr; 15(4):2247-2254. PubMed ID: 28259982
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. The ambiguous role of NKX2-5 mutations in thyroid dysgenesis.
van Engelen K; Mommersteeg MT; Baars MJ; Lam J; Ilgun A; van Trotsenburg AS; Smets AM; Christoffels VM; Mulder BJ; Postma AV
PLoS One; 2012; 7(12):e52685. PubMed ID: 23285148
[TBL] [Abstract][Full Text] [Related]
29. Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations.
Granados-Riveron JT; Pope M; Bu'lock FA; Thornborough C; Eason J; Setchfield K; Ketley A; Kirk EP; Fatkin D; Feneley MP; Harvey RP; Brook JD
Congenit Heart Dis; 2012; 7(2):151-9. PubMed ID: 22011241
[TBL] [Abstract][Full Text] [Related]
30. Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect.
Hirayama-Yamada K; Kamisago M; Akimoto K; Aotsuka H; Nakamura Y; Tomita H; Furutani M; Imamura S; Takao A; Nakazawa M; Matsuoka R
Am J Med Genet A; 2005 May; 135(1):47-52. PubMed ID: 15810002
[TBL] [Abstract][Full Text] [Related]
31. Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy.
Costa MW; Guo G; Wolstein O; Vale M; Castro ML; Wang L; Otway R; Riek P; Cochrane N; Furtado M; Semsarian C; Weintraub RG; Yeoh T; Hayward C; Keogh A; Macdonald P; Feneley M; Graham RM; Seidman JG; Seidman CE; Rosenthal N; Fatkin D; Harvey RP
Circ Cardiovasc Genet; 2013 Jun; 6(3):238-47. PubMed ID: 23661673
[TBL] [Abstract][Full Text] [Related]
32. Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects.
Salazar M; Consoli F; Villegas V; Caicedo V; Maddaloni V; Daniele P; Caianiello G; Pachón S; Nuñez F; Limongelli G; Pacileo G; Marino B; Bernal JE; De Luca A; Dallapiccola B
Eur J Med Genet; 2011; 54(3):306-9. PubMed ID: 21276881
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways.
Benson DW; Silberbach GM; Kavanaugh-McHugh A; Cottrill C; Zhang Y; Riggs S; Smalls O; Johnson MC; Watson MS; Seidman JG; Seidman CE; Plowden J; Kugler JD
J Clin Invest; 1999 Dec; 104(11):1567-73. PubMed ID: 10587520
[TBL] [Abstract][Full Text] [Related]
35. Congenital heart defect causing mutation in Nkx2.5 displays in vivo functional deficit.
Zakariyah AF; Rajgara RF; Veinot JP; Skerjanc IS; Burgon PG
J Mol Cell Cardiol; 2017 Apr; 105():89-98. PubMed ID: 28302382
[TBL] [Abstract][Full Text] [Related]
36. Two novel and functional DNA sequence variants within an upstream enhancer of the human NKX2-5 gene in ventricular septal defects.
Huang W; Meng H; Qiao Y; Pang S; Chen D; Yan B
Gene; 2013 Jul; 524(2):152-5. PubMed ID: 23644027
[TBL] [Abstract][Full Text] [Related]
37. A mouse model of human congenital heart disease: high incidence of diverse cardiac anomalies and ventricular noncompaction produced by heterozygous Nkx2-5 homeodomain missense mutation.
Ashraf H; Pradhan L; Chang EI; Terada R; Ryan NJ; Briggs LE; Chowdhury R; Zárate MA; Sugi Y; Nam HJ; Benson DW; Anderson RH; Kasahara H
Circ Cardiovasc Genet; 2014 Aug; 7(4):423-433. PubMed ID: 25028484
[TBL] [Abstract][Full Text] [Related]
38. Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors.
Sarkozy A; Conti E; Neri C; D'Agostino R; Digilio MC; Esposito G; Toscano A; Marino B; Pizzuti A; Dallapiccola B
J Med Genet; 2005 Feb; 42(2):e16. PubMed ID: 15689439
[No Abstract] [Full Text] [Related]
39. 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]
40. Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease.
Reamon-Buettner SM; Borlak J
J Med Genet; 2004 Sep; 41(9):684-90. PubMed ID: 15342699
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
