BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

392 related articles for article (PubMed ID: 20828405)

  • 21. Completion of the epithelial to mesenchymal transition in zebrafish mesoderm requires Spadetail.
    Row RH; Maître JL; Martin BL; Stockinger P; Heisenberg CP; Kimelman D
    Dev Biol; 2011 Jun; 354(1):102-10. PubMed ID: 21463614
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Interactions between Cdx genes and retinoic acid modulate early cardiogenesis.
    Lengerke C; Wingert R; Beeretz M; Grauer M; Schmidt AG; Konantz M; Daley GQ; Davidson AJ
    Dev Biol; 2011 Jun; 354(1):134-42. PubMed ID: 21466798
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The Osr1 and Osr2 genes act in the pronephric anlage downstream of retinoic acid signaling and upstream of Wnt2b to maintain pectoral fin development.
    Neto A; Mercader N; Gómez-Skarmeta JL
    Development; 2012 Jan; 139(2):301-11. PubMed ID: 22129829
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Retinoic acid negatively regulates dact3b expression in the hindbrain of zebrafish embryos.
    Mandal A; Waxman J
    Gene Expr Patterns; 2014 Nov; 16(2):122-9. PubMed ID: 25266145
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Fgf-driven Tbx protein activities directly induce
    Osborn DPS; Li K; Cutty SJ; Nelson AC; Wardle FC; Hinits Y; Hughes SM
    Development; 2020 Apr; 147(8):. PubMed ID: 32345657
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Zebrafish foxc1a plays a crucial role in early somitogenesis by restricting the expression of aldh1a2 directly.
    Li J; Yue Y; Dong X; Jia W; Li K; Liang D; Dong Z; Wang X; Nan X; Zhang Q; Zhao Q
    J Biol Chem; 2015 Apr; 290(16):10216-28. PubMed ID: 25724646
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Zebrafish wnt11: pattern and regulation of the expression by the yolk cell and No tail activity.
    Makita R; Mizuno T; Koshida S; Kuroiwa A; Takeda H
    Mech Dev; 1998 Feb; 71(1-2):165-76. PubMed ID: 9507106
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Fibin, a novel secreted lateral plate mesoderm signal, is essential for pectoral fin bud initiation in zebrafish.
    Wakahara T; Kusu N; Yamauchi H; Kimura I; Konishi M; Miyake A; Itoh N
    Dev Biol; 2007 Mar; 303(2):527-35. PubMed ID: 17196583
    [TBL] [Abstract][Full Text] [Related]  

  • 29. BMP signaling and spadetail regulate exit of muscle precursors from the zebrafish tailbud.
    O'Neill K; Thorpe C
    Dev Biol; 2013 Mar; 375(2):117-27. PubMed ID: 23246591
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Global identification of Smad2 and Eomesodermin targets in zebrafish identifies a conserved transcriptional network in mesendoderm and a novel role for Eomesodermin in repression of ectodermal gene expression.
    Nelson AC; Cutty SJ; Niini M; Stemple DL; Flicek P; Houart C; Bruce AE; Wardle FC
    BMC Biol; 2014 Oct; 12():81. PubMed ID: 25277163
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Wnt signaling is required for early development of zebrafish swimbladder.
    Yin A; Korzh S; Winata CL; Korzh V; Gong Z
    PLoS One; 2011 Mar; 6(3):e18431. PubMed ID: 21479192
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Transgenic zebrafish recapitulating tbx16 gene early developmental expression.
    Wells S; Nornes S; Lardelli M
    PLoS One; 2011; 6(6):e21559. PubMed ID: 21720556
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The role of the SPT6 chromatin remodeling factor in zebrafish embryogenesis.
    Kok FO; Oster E; Mentzer L; Hsieh JC; Henry CA; Sirotkin HI
    Dev Biol; 2007 Jul; 307(2):214-26. PubMed ID: 17570355
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Coordination of symmetric cyclic gene expression during somitogenesis by Suppressor of Hairless involves regulation of retinoic acid catabolism.
    Echeverri K; Oates AC
    Dev Biol; 2007 Jan; 301(2):388-403. PubMed ID: 17098223
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The zebrafish T-box genes no tail and spadetail are required for development of trunk and tail mesoderm and medial floor plate.
    Amacher SL; Draper BW; Summers BR; Kimmel CB
    Development; 2002 Jul; 129(14):3311-23. PubMed ID: 12091302
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification of in vivo Hox13-binding sites reveals an essential locus controlling zebrafish brachyury expression.
    Ye Z; Braden CR; Wills A; Kimelman D
    Development; 2021 Jun; 148(11):. PubMed ID: 34061173
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Wnt signaling balances specification of the cardiac and pharyngeal muscle fields.
    Mandal A; Holowiecki A; Song YC; Waxman JS
    Mech Dev; 2017 Feb; 143():32-41. PubMed ID: 28087459
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Distinct phases of Wnt/β-catenin signaling direct cardiomyocyte formation in zebrafish.
    Dohn TE; Waxman JS
    Dev Biol; 2012 Jan; 361(2):364-76. PubMed ID: 22094017
    [TBL] [Abstract][Full Text] [Related]  

  • 39. FGF and canonical Wnt signaling cooperate to induce paraxial mesoderm from tailbud neuromesodermal progenitors through regulation of a two-step epithelial to mesenchymal transition.
    Goto H; Kimmey SC; Row RH; Matus DQ; Martin BL
    Development; 2017 Apr; 144(8):1412-1424. PubMed ID: 28242612
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A novel cold-sensitive mutant of ntla reveals temporal roles of brachyury in zebrafish.
    Kimelman D
    Dev Dyn; 2016 Aug; 245(8):874-80. PubMed ID: 27153483
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.