BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 1763820)

  • 1. Endothelial cell origin and migration in embryonic heart and cranial blood vessel development.
    Coffin JD; Poole TJ
    Anat Rec; 1991 Nov; 231(3):383-95. PubMed ID: 1763820
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Vasculogenesis and angiogenesis: two distinct morphogenetic mechanisms establish embryonic vascular pattern.
    Poole TJ; Coffin JD
    J Exp Zool; 1989 Aug; 251(2):224-31. PubMed ID: 2671254
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Formation and early morphogenesis of endocardial endothelial precursor cells and the role of endoderm.
    Sugi Y; Markwald RR
    Dev Biol; 1996 Apr; 175(1):66-83. PubMed ID: 8608870
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Assembly of trunk and limb blood vessels involves extensive migration and vasculogenesis of somite-derived angioblasts.
    Ambler CA; Nowicki JL; Burke AC; Bautch VL
    Dev Biol; 2001 Jun; 234(2):352-64. PubMed ID: 11397005
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Angioblast differentiation is influenced by the local environment: FGF-2 induces angioblasts and patterns vessel formation in the quail embryo.
    Cox CM; Poole TJ
    Dev Dyn; 2000 Jun; 218(2):371-82. PubMed ID: 10842363
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The proepicardium delivers hemangioblasts but not lymphangioblasts to the developing heart.
    Wilting J; Buttler K; Schulte I; Papoutsi M; Schweigerer L; Männer J
    Dev Biol; 2007 May; 305(2):451-9. PubMed ID: 17383624
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Vasculogenesis of the embryonic heart: origin of blood island-like structures.
    Ratajska A; Czarnowska E; Kołodzińska A; Kluzek W; Leśniak W
    Anat Rec A Discov Mol Cell Evol Biol; 2006 Mar; 288(3):223-32. PubMed ID: 16463372
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The role of FGF and VEGF in angioblast induction and migration during vascular development.
    Poole TJ; Finkelstein EB; Cox CM
    Dev Dyn; 2001 Jan; 220(1):1-17. PubMed ID: 11146503
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Early endocardial formation originates from precardiac mesoderm as revealed by QH-1 antibody staining.
    Sugi Y; Markwald RR
    Ital J Anat Embryol; 1995; 100 Suppl 1():263-72. PubMed ID: 11322300
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Formation and remodeling of the coronary vascular bed in the embryonic avian heart.
    Kattan J; Dettman RW; Bristow J
    Dev Dyn; 2004 May; 230(1):34-43. PubMed ID: 15108307
    [TBL] [Abstract][Full Text] [Related]  

  • 11. In vivo and in vitro analysis of the vasculogenic potential of avian proepicardial and epicardial cells.
    Guadix JA; Carmona R; Muñoz-Chápuli R; Pérez-Pomares JM
    Dev Dyn; 2006 Apr; 235(4):1014-26. PubMed ID: 16456846
    [TBL] [Abstract][Full Text] [Related]  

  • 12. First blood vessels in the avian neural tube are formed by a combination of dorsal angioblast immigration and ventral sprouting of endothelial cells.
    Kurz H; Gärtner T; Eggli PS; Christ B
    Dev Biol; 1996 Jan; 173(1):133-47. PubMed ID: 8575615
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel mouse endothelial cell surface marker is suppressed during differentiation of the blood brain barrier.
    Hallmann R; Mayer DN; Berg EL; Broermann R; Butcher EC
    Dev Dyn; 1995 Apr; 202(4):325-32. PubMed ID: 7626790
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early heart development: dynamics of endocardial cell sorting suggests a common origin with cardiomyocytes.
    Linask KK; Lash JW
    Dev Dyn; 1993 Jan; 196(1):62-9. PubMed ID: 8334299
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mixed cultures of avian blastoderm cells and the quail mesoderm cell line QCE-6 provide evidence for the pluripotentiality of early mesoderm.
    Eisenberg CA; Markwald RR
    Dev Biol; 1997 Nov; 191(2):167-81. PubMed ID: 9398432
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Blood vessel formation in the avian limb bud involves angioblastic and angiotrophic growth.
    Brand-Saberi B; Seifert R; Grim M; Wilting J; Kühlewein M; Christ B
    Dev Dyn; 1995 Feb; 202(2):181-94. PubMed ID: 7734735
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Myocardial heterogeneity in permissiveness for epicardium-derived cells and endothelial precursor cells along the developing heart tube at the onset of coronary vascularization.
    Lie-Venema H; Eralp I; Maas S; Gittenberger-De Groot AC; Poelmann RE; DeRuiter MC
    Anat Rec A Discov Mol Cell Evol Biol; 2005 Feb; 282(2):120-9. PubMed ID: 15627984
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Angiogenic potential of the avian somite.
    Wilting J; Brand-Saberi B; Huang R; Zhi Q; Köntges G; Ordahl CP; Christ B
    Dev Dyn; 1995 Feb; 202(2):165-71. PubMed ID: 7537553
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Common epicardial origin of coronary vascular smooth muscle, perivascular fibroblasts, and intermyocardial fibroblasts in the avian heart.
    Dettman RW; Denetclaw W; Ordahl CP; Bristow J
    Dev Biol; 1998 Jan; 193(2):169-81. PubMed ID: 9473322
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Developing blood vessels and associated extracellular matrix as substrates for neural crest migration in Japanese quail, Coturnix coturnix japonica.
    Spence SG; Poole TJ
    Int J Dev Biol; 1994 Mar; 38(1):85-98. PubMed ID: 7521199
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.