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 *

100 related articles for article (PubMed ID: 18375255)

  • 1. Clinical and genetic investigation of atrial septal defect with atrioventricular conduction defect in a large consanguineous Tunisian family.
    Nouira S; Kamoun I; Ouragini H; Charfeddine C; Mahjoub H; Ouechtati F; Bchetnia M; Ben Halima A; Abdelhak S; Kachboura S
    Arch Med Res; 2008 May; 39(4):429-33. PubMed ID: 18375255
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial atrial septal defect in the oval fossa with progressive prolongation of the atrioventricular conduction caused by mutations in the NKX2.5 gene.
    Bjørnstad PG; Leren TP
    Cardiol Young; 2009 Feb; 19(1):40-4. PubMed ID: 19049681
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa.
    Rifai L; Maazouzi W; Sefiani A
    Cardiol Young; 2007 Feb; 17(1):107-9. PubMed ID: 17184575
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Familial atrial septal defect and atrioventricular conduction disturbance associated with a point mutation in the cardiac homeobox gene CSX/NKX2-5 in a Japanese patient.
    Hosoda T; Komuro I; Shiojima I; Hiroi Y; Harada M; Murakawa Y; Hirata Y; Yazaki Y
    Jpn Circ J; 1999 May; 63(5):425-6. PubMed ID: 10943630
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. [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]  

  • 9. Familial atrial septal defect with atrioventricular conduction defects.
    Mandorla S; Martino C
    G Ital Cardiol; 1998 Mar; 28(3):294-6. PubMed ID: 9561886
    [TBL] [Abstract][Full Text] [Related]  

  • 10. NKX2-5 mutations in an inbred consanguineous population: genetic and phenotypic diversity.
    Abou Hassan OK; Fahed AC; Batrawi M; Arabi M; Refaat MM; DePalma SR; Seidman JG; Seidman CE; Bitar FF; Nemer GM
    Sci Rep; 2015 Mar; 5():8848. PubMed ID: 25742962
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?
    Gutierrez-Roelens I; De Roy L; Ovaert C; Sluysmans T; Devriendt K; Brunner HG; Vikkula M
    Eur J Hum Genet; 2006 Dec; 14(12):1313-6. PubMed ID: 16896344
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Aspect of NK2 Transcription Factor Related Locus-5 (NKX2.5) Gene Mutations in Bangladeshi Atrial Septal Defect (ASD) patients and 2D Relationship with their Age.
    Roy RR; Sultana GN; Begum R; Shahinuzzaman AD; Sharif MI
    Mymensingh Med J; 2016 Jan; 25(1):79-84. PubMed ID: 26931254
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. A mouse model of congenital heart disease: cardiac arrhythmias and atrial septal defect caused by haploinsufficiency of the cardiac transcription factor Csx/Nkx2.5.
    Tanaka M; Berul CI; Ishii M; Jay PY; Wakimoto H; Douglas P; Yamasaki N; Kawamoto T; Gehrmann J; Maguire CT; Schinke M; Seidman CE; Seidman JG; Kurachi Y; Izumo S
    Cold Spring Harb Symp Quant Biol; 2002; 67():317-25. PubMed ID: 12858555
    [No Abstract]   [Full Text] [Related]  

  • 19. Novel and highly lethal NKX2.5 missense mutation in a family with sudden death and ventricular arrhythmia.
    Perera JL; Johnson NM; Judge DP; Crosson JE
    Pediatr Cardiol; 2014 Oct; 35(7):1206-12. PubMed ID: 24880466
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Gene mutation in secundum atrial septal defect: analysis of a Chinese family with 3 patients].
    Tian L; Zhu JF; Yang JG; Zhu QH; Du R; Li J; Li W
    Zhonghua Yi Xue Za Zhi; 2008 Jan; 88(4):250-3. PubMed ID: 18361836
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.