These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 36011517)

  • 1. 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]  

  • 2. Genetic and functional analysis of the NKX2-5 gene promoter in patients with ventricular septal defects.
    Pang S; Shan J; Qiao Y; Ma L; Qin X; Wanyan H; Xing Q; Wu G; Yan B
    Pediatr Cardiol; 2012 Dec; 33(8):1355-61. PubMed ID: 22576768
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Novel NKX2-5 germline mutation in a Moroccan child with transitional atrio-ventricular septal defect (tAVSD).
    El-Bouchikhi I; Belhassan K; Moufid FZ; Houssaini MI; Ouldim K; Atmani S
    Turk J Pediatr; 2017; 59(5):610-613. PubMed ID: 29745128
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Genetic analysis of an enhancer of the NKX2-5 gene in ventricular septal defects.
    Qin X; Xing Q; Ma L; Meng H; Liu Y; Pang S; Yan B
    Gene; 2012 Oct; 508(1):106-9. PubMed ID: 22824467
    [TBL] [Abstract][Full Text] [Related]  

  • 8. R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease.
    Beffagna G; Cecchetto A; Dal Bianco L; Lorenzon A; Angelini A; Padalino M; Vida V; Bhattacharya S; Stellin G; Rampazzo A; Daliento L
    J Cardiovasc Med (Hagerstown); 2013 Aug; 14(8):582-6. PubMed ID: 22964646
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Congenital heart defects are rarely caused by mutations in cardiac and smooth muscle actin genes.
    Khodyuchenko T; Zlotina A; Pervunina T; Zverev D; Malashicheva A; Kostareva A
    Biomed Res Int; 2015; 2015():127807. PubMed ID: 25861618
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. [Novel NKX2-5 mutations identified in patients with congenital ventricular septal defects].
    Liu XY; Yang YQ; Yang Y; Lin XP; Chen YH
    Zhonghua Yi Xue Za Zhi; 2009 Sep; 89(34):2395-9. PubMed ID: 20137692
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Functional analysis of novel genetic variants of NKX2-5 associated with nonsyndromic congenital heart disease.
    Dixit R; Narasimhan C; Balekundri VI; Agrawal D; Kumar A; Mohapatra B
    Am J Med Genet A; 2021 Dec; 185(12):3644-3663. PubMed ID: 34214246
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations of the GATA4 and NKX2.5 genes in Chinese pediatric patients with non-familial congenital heart disease.
    Peng T; Wang L; Zhou SF; Li X
    Genetica; 2010 Dec; 138(11-12):1231-40. PubMed ID: 21110066
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel stop mutation truncating critical regions of the cardiac transcription factor NKX2-5 in a large family with autosomal-dominant inherited congenital heart disease.
    Pabst S; Wollnik B; Rohmann E; Hintz Y; Glänzer K; Vetter H; Nickenig G; Grohé C
    Clin Res Cardiol; 2008 Jan; 97(1):39-42. PubMed ID: 17891520
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.