176 related articles for article (PubMed ID: 30982828)
1. 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]
2. 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]
3. 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]
4. 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]
5. [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]
6. Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children.
Behiry EG; Al-Azzouny MA; Sabry D; Behairy OG; Salem NE
Mol Genet Genomic Med; 2019 May; 7(5):e612. PubMed ID: 30834692
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. NKX2-5 molecular screening and assessment of variant rate and risk factors of secundum atrial septal defect in a Moroccan population.
El Bouchikhi I; Bouguenouch L; Zohra Moufid F; Houssaini MI; Belhassan K; Samri I; Joutei AT; Ouldim K; Atmani S
Anatol J Cardiol; 2017 Mar; 17(3):217-223. PubMed ID: 27752029
[TBL] [Abstract][Full Text] [Related]
9. Single nucleotide polymorphism of NKX2-5 gene with sporadic congenital heart disease in Chinese Bai population.
Cao Y; Lan W; Li Y; Wei C; Zou H; Jiang L
Int J Clin Exp Pathol; 2015; 8(11):14917-24. PubMed ID: 26823822
[TBL] [Abstract][Full Text] [Related]
10. Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.
Elliott DA; Kirk EP; Yeoh T; Chandar S; McKenzie F; Taylor P; Grossfeld P; Fatkin D; Jones O; Hayes P; Feneley M; Harvey RP
J Am Coll Cardiol; 2003 Jun; 41(11):2072-6. PubMed ID: 12798584
[TBL] [Abstract][Full Text] [Related]
11. Investigation of somatic NKX2-5 mutations in congenital heart disease.
Draus JM; Hauck MA; Goetsch M; Austin EH; Tomita-Mitchell A; Mitchell ME
J Med Genet; 2009 Feb; 46(2):115-22. PubMed ID: 19181906
[TBL] [Abstract][Full Text] [Related]
12. Search of Somatic Mutations of NKX2-5 and GATA4 Genes in Chinese Patients with Sporadic Congenital Heart Disease.
Yin J; Qian J; Dai G; Wang C; Qin Y; Xu T; Li Z; Zhang H; Yang S
Pediatr Cardiol; 2019 Jan; 40(1):17-22. PubMed ID: 30121862
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Mutational Assessment in
Nazeer NU; Bhat MA; Rah B; Bhat GR; Wani SI; Yousuf A; Dar AM; Afroze D
Int J Environ Res Public Health; 2022 Aug; 19(16):. PubMed ID: 36011517
[TBL] [Abstract][Full Text] [Related]
15. Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease.
Xiong F; Li Q; Zhang C; Chen Y; Li P; Wei X; Li Q; Zhou W; Li L; Shang X; Xu X
Cardiovasc Pathol; 2013; 22(2):141-5. PubMed ID: 22959235
[TBL] [Abstract][Full Text] [Related]
16. Novel Point Mutations in the
Khatami M; Mazidi M; Taher S; Heidari MM; Hadadzadeh M
Medicina (Kaunas); 2018 Jun; 54(3):. PubMed ID: 30344277
[No Abstract] [Full Text] [Related]
17. A de novo mutation in NKX2.5 associated with atrial septal defects, ventricular noncompaction, syncope and sudden death.
Ouyang P; Saarel E; Bai Y; Luo C; Lv Q; Xu Y; Wang F; Fan C; Younoszai A; Chen Q; Tu X; Wang QK
Clin Chim Acta; 2011 Jan; 412(1-2):170-5. PubMed ID: 20932824
[TBL] [Abstract][Full Text] [Related]
18. Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature.
Ellesøe SG; Johansen MM; Bjerre JV; Hjortdal VE; Brunak S; Larsen LA
Congenit Heart Dis; 2016 May; 11(3):283-90. PubMed ID: 26679770
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Associations between two genetic variants in NKX2-5 and risk of congenital heart disease in Chinese population: a meta-analysis.
Wang Z; Zou L; Zhong R; Zhu B; Chen W; Shen N; Ke J; Lou J; Song R; Miao XP
PLoS One; 2013; 8(8):e70979. PubMed ID: 23936479
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
