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 *

166 related articles for article (PubMed ID: 22534315)

  • 1. Complex trait analysis of ventricular septal defects caused by Nkx2-5 mutation.
    Winston JB; Schulkey CE; Chen IB; Regmi SD; Efimova M; Erlich JM; Green CA; Aluko A; Jay PY
    Circ Cardiovasc Genet; 2012 Jun; 5(3):293-300. PubMed ID: 22534315
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Heterogeneity of genetic modifiers ensures normal cardiac development.
    Winston JB; Erlich JM; Green CA; Aluko A; Kaiser KA; Takematsu M; Barlow RS; Sureka AO; LaPage MJ; Janss LL; Jay PY
    Circulation; 2010 Mar; 121(11):1313-21. PubMed ID: 20212279
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel NKX2-5 mutation in familial ventricular septal defect.
    Wang J; Xin YF; Liu XY; Liu ZM; Wang XZ; Yang YQ
    Int J Mol Med; 2011 Mar; 27(3):369-75. PubMed ID: 21165553
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. A novel NKX2.6 mutation associated with congenital ventricular septal defect.
    Wang J; Mao JH; Ding KK; Xu WJ; Liu XY; Qiu XB; Li RG; Qu XK; Xu YJ; Huang RT; Xue S; Yang YQ
    Pediatr Cardiol; 2015 Mar; 36(3):646-56. PubMed ID: 25380965
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Nkx2-5 and Sarcospan genetically interact in the development of the muscular ventricular septum of the heart.
    Panzer AA; Regmi SD; Cormier D; Danzo MT; Chen ID; Winston JB; Hutchinson AK; Salm D; Schulkey CE; Cochran RS; Wilson DB; Jay PY
    Sci Rep; 2017 Apr; 7():46438. PubMed ID: 28406175
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. Congenital heart disease caused by mutations in the transcription factor NKX2-5.
    Schott JJ; Benson DW; Basson CT; Pease W; Silberbach GM; Moak JP; Maron BJ; Seidman CE; Seidman JG
    Science; 1998 Jul; 281(5373):108-11. PubMed ID: 9651244
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Cardiac septal and valvular dysmorphogenesis in mice heterozygous for mutations in the homeobox gene Nkx2-5.
    Biben C; Weber R; Kesteven S; Stanley E; McDonald L; Elliott DA; Barnett L; Köentgen F; Robb L; Feneley M; Harvey RP
    Circ Res; 2000 Nov; 87(10):888-95. PubMed ID: 11073884
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Human Genetics of Ventricular Septal Defect.
    Perrot A; Rickert-Sperling S
    Adv Exp Med Biol; 2024; 1441():505-534. PubMed ID: 38884729
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.