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 *

96 related articles for article (PubMed ID: 25818641)

  • 1. The expression profile analysis of NKX2-5 knock-out embryonic mice to explore the pathogenesis of congenital heart disease.
    Li J; Cao Y; Wu Y; Chen W; Yuan Y; Ma X; Huang G
    J Cardiol; 2015 Dec; 66(6):527-31. PubMed ID: 25818641
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Transcriptional Regulatory Network Analysis for Gastric Cancer Based on mRNA Microarray.
    Wang Y
    Pathol Oncol Res; 2017 Oct; 23(4):785-791. PubMed ID: 28078605
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. An Anterior Second Heart Field Enhancer Regulates the Gene Regulatory Network of the Cardiac Outflow Tract.
    Yamaguchi N; Chang EW; Lin Z; Shekhar A; Bu L; Khodadadi-Jamayran A; Tsirigos A; Cen Y; Phoon CKL; Moskowitz IP; Park DS
    Circulation; 2023 Nov; 148(21):1705-1722. PubMed ID: 37772400
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular mechanisms underlying gliomas and glioblastoma pathogenesis revealed by bioinformatics analysis of microarray data.
    Vastrad B; Vastrad C; Godavarthi A; Chandrashekar R
    Med Oncol; 2017 Sep; 34(11):182. PubMed ID: 28952134
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of Skt11-regulated genes in chondrocytes by integrated bioinformatics analysis.
    Liang S; Zhang JM; Lv ZT; Cheng P; Zhu WT; Chen AM
    Gene; 2018 Nov; 677():340-348. PubMed ID: 30107230
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Direct activation of a GATA6 cardiac enhancer by Nkx2.5: evidence for a reinforcing regulatory network of Nkx2.5 and GATA transcription factors in the developing heart.
    Molkentin JD; Antos C; Mercer B; Taigen T; Miano JM; Olson EN
    Dev Biol; 2000 Jan; 217(2):301-9. PubMed ID: 10625555
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Nkx2-5 pathways and congenital heart disease; loss of ventricular myocyte lineage specification leads to progressive cardiomyopathy and complete heart block.
    Pashmforoush M; Lu JT; Chen H; Amand TS; Kondo R; Pradervand S; Evans SM; Clark B; Feramisco JR; Giles W; Ho SY; Benson DW; Silberbach M; Shou W; Chien KR
    Cell; 2004 Apr; 117(3):373-86. PubMed ID: 15109497
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Nuclear Receptor-Like Structure and Interaction of Congenital Heart Disease-Associated Factors GATA4 and NKX2-5.
    Kinnunen S; Välimäki M; Tölli M; Wohlfahrt G; Darwich R; Komati H; Nemer M; Ruskoaho H
    PLoS One; 2015; 10(12):e0144145. PubMed ID: 26642209
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Progressive atrioventricular conduction defects and heart failure in mice expressing a mutant Csx/Nkx2.5 homeoprotein.
    Kasahara H; Wakimoto H; Liu M; Maguire CT; Converso KL; Shioi T; Huang WY; Manning WJ; Paul D; Lawitts J; Berul CI; Izumo S
    J Clin Invest; 2001 Jul; 108(2):189-201. PubMed ID: 11457872
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of differentially expressed genes regulated by transcription factors in glioblastomas by bioinformatics analysis.
    Wei B; Wang L; Du C; Hu G; Wang L; Jin Y; Kong D
    Mol Med Rep; 2015 Apr; 11(4):2548-54. PubMed ID: 25514975
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gene expression changes in human mesenchymal stem cells from patients with osteoporosis.
    Liu L; Zhu Q; Wang J; Xi Q; Zhu H; Gu M
    Mol Med Rep; 2015 Jul; 12(1):981-7. PubMed ID: 25815782
    [TBL] [Abstract][Full Text] [Related]  

  • 15. In Vitro Modeling of Congenital Heart Defects Associated with an NKX2-5 Mutation Revealed a Dysregulation in BMP/Notch-Mediated Signaling.
    Zakariyah AF; Rajgara RF; Horner E; Cattin ME; Blais A; Skerjanc IS; Burgon PG
    Stem Cells; 2018 Apr; 36(4):514-526. PubMed ID: 29282804
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A tyrosine-rich domain within homeodomain transcription factor Nkx2-5 is an essential element in the early cardiac transcriptional regulatory machinery.
    Elliott DA; Solloway MJ; Wise N; Biben C; Costa MW; Furtado MB; Lange M; Dunwoodie S; Harvey RP
    Development; 2006 Apr; 133(7):1311-22. PubMed ID: 16510504
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Uncovering potential key genes associated with the pathogenesis of asthma: A microarray analysis of asthma-relevant tissues.
    Guan Y; Jin X; Liu X; Huang Y; Wang M; Li X
    Allergol Immunopathol (Madr); 2017; 45(2):152-159. PubMed ID: 27842724
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Screening key genes associated with congenital heart defects in Down syndrome based on differential expression network.
    Yu S; Yi H; Wang Z; Dong J
    Int J Clin Exp Pathol; 2015; 8(7):8385-93. PubMed ID: 26339408
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Preliminary exploration of transcription factor Nkx2.5 mutations and congenital heart diseases].
    Ding JD; Li KR; Zhang XL; Yao YY; Reng LQ; Tao SY; Fang X; Ma GS
    Zhonghua Yi Xue Za Zhi; 2009 Apr; 89(16):1114-6. PubMed ID: 19595143
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Absence of Msx2 does not affect cardiac conduction or rescue conduction defects associated with Nkx2-5 mutation.
    Jay PY; Maguire CT; Wakimoto H; Izumo S; Berul CI
    J Cardiovasc Electrophysiol; 2005 Jan; 16(1):82-5. PubMed ID: 15673394
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.