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 *

233 related articles for article (PubMed ID: 12074273)

  • 41. 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]  

  • 42. The cardiac tissue-restricted homeobox protein Csx/Nkx2.5 physically associates with the zinc finger protein GATA4 and cooperatively activates atrial natriuretic factor gene expression.
    Lee Y; Shioi T; Kasahara H; Jobe SM; Wiese RJ; Markham BE; Izumo S
    Mol Cell Biol; 1998 Jun; 18(6):3120-9. PubMed ID: 9584153
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Congenital heart diseases and their association with the variant distribution features on susceptibility genes.
    Su W; Zhu P; Wang R; Wu Q; Wang M; Zhang X; Mei L; Tang J; Kumar M; Wang X; Su L; Dong N
    Clin Genet; 2017 Mar; 91(3):349-354. PubMed ID: 27426723
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Cardiac expression of the ventricle-specific homeobox gene Irx4 is modulated by Nkx2-5 and dHand.
    Bruneau BG; Bao ZZ; Tanaka M; Schott JJ; Izumo S; Cepko CL; Seidman JG; Seidman CE
    Dev Biol; 2000 Jan; 217(2):266-77. PubMed ID: 10625552
    [TBL] [Abstract][Full Text] [Related]  

  • 45. 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]  

  • 46. 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]  

  • 47. 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]  

  • 48. [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]  

  • 49. 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]  

  • 50. Cardiac and extracardiac expression of Csx/Nkx2.5 homeodomain protein.
    Kasahara H; Bartunkova S; Schinke M; Tanaka M; Izumo S
    Circ Res; 1998 May; 82(9):936-46. PubMed ID: 9598591
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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]  

  • 52. 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]  

  • 53. 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]  

  • 54. Zac1 is an essential transcription factor for cardiac morphogenesis.
    Yuasa S; Onizuka T; Shimoji K; Ohno Y; Kageyama T; Yoon SH; Egashira T; Seki T; Hashimoto H; Nishiyama T; Kaneda R; Murata M; Hattori F; Makino S; Sano M; Ogawa S; Prall OW; Harvey RP; Fukuda K
    Circ Res; 2010 Apr; 106(6):1083-91. PubMed ID: 20167925
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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]  

  • 56. Identification of TBX5 mutations in a series of 94 patients with Tetralogy of Fallot.
    Baban A; Postma AV; Marini M; Trocchio G; Santilli A; Pelegrini M; Sirleto P; Lerone M; Albanese SB; Barnett P; Boogerd CJ; Dallapiccola B; Digilio MC; Ravazzolo R; Pongiglione G
    Am J Med Genet A; 2014 Dec; 164A(12):3100-7. PubMed ID: 25263169
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Mouse Model of Human Congenital Heart Disease: Progressive Atrioventricular Block Induced by a Heterozygous Nkx2-5 Homeodomain Missense Mutation.
    Chowdhury R; Ashraf H; Melanson M; Tanada Y; Nguyen M; Silberbach M; Wakimoto H; Benson DW; Anderson RH; Kasahara H
    Circ Arrhythm Electrophysiol; 2015 Oct; 8(5):1255-64. PubMed ID: 26226998
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Divergent roles for NK-2 class homeobox genes in cardiogenesis in flies and mice.
    Ranganayakulu G; Elliott DA; Harvey RP; Olson EN
    Development; 1998 Aug; 125(16):3037-48. PubMed ID: 9671578
    [TBL] [Abstract][Full Text] [Related]  

  • 59. GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.
    Garg V; Kathiriya IS; Barnes R; Schluterman MK; King IN; Butler CA; Rothrock CR; Eapen RS; Hirayama-Yamada K; Joo K; Matsuoka R; Cohen JC; Srivastava D
    Nature; 2003 Jul; 424(6947):443-7. PubMed ID: 12845333
    [TBL] [Abstract][Full Text] [Related]  

  • 60. The combinatorial activities of Nkx2.5 and dHAND are essential for cardiac ventricle formation.
    Yamagishi H; Yamagishi C; Nakagawa O; Harvey RP; Olson EN; Srivastava D
    Dev Biol; 2001 Nov; 239(2):190-203. PubMed ID: 11784028
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.