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 *

141 related articles for article (PubMed ID: 21262546)

  • 21. Progressive AV-block and anomalous venous return among cardiac anomalies associated with two novel missense mutations in the CSX/NKX2-5 gene.
    Gutierrez-Roelens I; Sluysmans T; Gewillig M; Devriendt K; Vikkula M
    Hum Mutat; 2002 Jul; 20(1):75-6. PubMed ID: 12112663
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. NKX2.5/NKX2.6 mutations are not a common cause of isolated type 1 truncus arteriosus in a small cohort of multiethnic cases.
    Khetyar M; Tinworth L; Syrris P; Abushaban L; Abdulazzaq Y; Silengo M; Carvalho J; Carter N
    Genet Test; 2008 Dec; 12(4):467-9. PubMed ID: 18939937
    [No Abstract]   [Full Text] [Related]  

  • 25. 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]  

  • 26. Somatic mutations in cardiac malformations.
    Reamon-Buettner SM; Borlak J
    J Med Genet; 2006 Aug; 43(8):e45. PubMed ID: 16882739
    [No Abstract]   [Full Text] [Related]  

  • 27. Molecular basis of AV block and cardiac malformations.
    Mittmann C
    Cardiovasc Res; 2004 Oct; 64(1):1-2. PubMed ID: 15364605
    [No Abstract]   [Full Text] [Related]  

  • 28. The effect of p.Arg25Cys alteration in NKX2-5 on conotruncal heart anomalies: mutation or polymorphism?
    Akçaboy MI; Cengiz FB; Inceoğlu B; Uçar T; Atalay S; Tutar E; Tekin M
    Pediatr Cardiol; 2008 Jan; 29(1):126-9. PubMed ID: 17891434
    [TBL] [Abstract][Full Text] [Related]  

  • 29. NKX2-5: an update on this hypermutable homeodomain protein and its role in human congenital heart disease (CHD).
    Reamon-Buettner SM; Borlak J
    Hum Mutat; 2010 Nov; 31(11):1185-94. PubMed ID: 20725931
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Insights into the genetic structure of congenital heart disease from human and murine studies on monogenic disorders.
    Prendiville T; Jay PY; Pu WT
    Cold Spring Harb Perspect Med; 2014 Oct; 4(10):. PubMed ID: 25274754
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. [Progress in studies on somatic mutations in congenital heart disease].
    Yin J; Yang SW; Qin YM
    Zhonghua Er Ke Za Zhi; 2012 Aug; 50(8):634-5. PubMed ID: 23158746
    [No Abstract]   [Full Text] [Related]  

  • 35. Transcriptional defect of an inherited NKX2-5 haplotype comprising a SNP, a nonsynonymous and a synonymous mutation, associated with human congenital heart disease.
    Reamon-Buettner SM; Sattlegger E; Ciribilli Y; Inga A; Wessel A; Borlak J
    PLoS One; 2013; 8(12):e83295. PubMed ID: 24376681
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Transient early embryonic expression of Nkx2-5 mutations linked to congenital heart defects in human causes heart defects in Xenopus laevis.
    Bartlett HL; Sutherland L; Kolker SJ; Welp C; Tajchman U; Desmarais V; Weeks DL
    Dev Dyn; 2007 Sep; 236(9):2475-84. PubMed ID: 17685485
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Crystal structure of the human NKX2.5 homeodomain in complex with DNA target.
    Pradhan L; Genis C; Scone P; Weinberg EO; Kasahara H; Nam HJ
    Biochemistry; 2012 Aug; 51(32):6312-9. PubMed ID: 22849347
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Nkx genes establish second heart field cardiomyocyte progenitors at the arterial pole and pattern the venous pole through Isl1 repression.
    Colombo S; de Sena-Tomás C; George V; Werdich AA; Kapur S; MacRae CA; Targoff KL
    Development; 2018 Feb; 145(3):. PubMed ID: 29361575
    [No Abstract]   [Full Text] [Related]  

  • 39. Heart disease: an ongoing genetic battle?
    Srivastava D
    Nature; 2004 Jun; 429(6994):819-22. PubMed ID: 15215849
    [No Abstract]   [Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.