BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

101 related articles for article (PubMed ID: 3288526)

  • 1. Cell polarity in sea urchin embryos: reorientation of cells occurs quickly in aggregates.
    Nelson SH; McClay DR
    Dev Biol; 1988 Jun; 127(2):235-47. PubMed ID: 3288526
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Archenteron elongation in the sea urchin embryo is a microtubule-independent process.
    Hardin JD
    Dev Biol; 1987 May; 121(1):253-62. PubMed ID: 3552789
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Measurements of mechanical properties of the blastula wall reveal which hypothesized mechanisms of primary invagination are physically plausible in the sea urchin Strongylocentrotus purpuratus.
    Davidson LA; Oster GF; Keller RE; Koehl MA
    Dev Biol; 1999 May; 209(2):221-38. PubMed ID: 10328917
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sea urchin primary mesenchyme cells: ingression occurs independent of microtubules.
    Anstrom JA
    Dev Biol; 1989 Jan; 131(1):269-75. PubMed ID: 2562830
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The cytoskeleton, endocytosis and cell polarity in the mouse preimplantation embryo.
    Fleming TP; Cannon PM; Pickering SJ
    Dev Biol; 1986 Feb; 113(2):406-19. PubMed ID: 3512332
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Storage and mobilization of extracellular matrix proteins during sea urchin development.
    Alliegro MC; McClay DR
    Dev Biol; 1988 Jan; 125(1):208-16. PubMed ID: 2445608
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Sea urchin primary mesenchyme cells: relation of cell polarity to the epithelial-mesenchymal transformation.
    Anstrom JA; Raff RA
    Dev Biol; 1988 Nov; 130(1):57-66. PubMed ID: 3053298
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Microtubules and actin filaments are not critically involved in the biogenesis of epithelial cell surface polarity.
    Salas PJ; Misek DE; Vega-Salas DE; Gundersen D; Cereijido M; Rodriguez-Boulan E
    J Cell Biol; 1986 May; 102(5):1853-67. PubMed ID: 2871031
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A dissection of the mechanisms generating and stabilizing polarity in mouse 8- and 16-cell blastomeres: the role of cytoskeletal elements.
    Johnson MH; Maro B
    J Embryol Exp Morphol; 1985 Dec; 90():311-34. PubMed ID: 2871124
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An N-linked carbohydrate-containing extracellular matrix determinant plays a key role in sea urchin gastrulation.
    Ingersoll EP; Ettensohn CA
    Dev Biol; 1994 Jun; 163(2):351-66. PubMed ID: 7515360
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The apical lamina and its role in cell adhesion in sea urchin embryos.
    Burke RD; Lail M; Nakajima Y
    Cell Adhes Commun; 1998 Mar; 5(2):97-108. PubMed ID: 9638331
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The cortical microfilament system of lymphoblasts displays a periodic oscillatory activity in the absence of microtubules: implications for cell polarity.
    Bornens M; Paintrand M; Celati C
    J Cell Biol; 1989 Sep; 109(3):1071-83. PubMed ID: 2570076
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sea urchin oocytes possess elaborate cortical arrays of microfilaments, microtubules, and intermediate filaments.
    Boyle JA; Ernst SG
    Dev Biol; 1989 Jul; 134(1):72-84. PubMed ID: 2471666
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cell polarity emerges at first cleavage in sea urchin embryos.
    Alford LM; Ng MM; Burgess DR
    Dev Biol; 2009 Jun; 330(1):12-20. PubMed ID: 19298809
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Three cell recognition changes accompany the ingression of sea urchin primary mesenchyme cells.
    Fink RD; McClay DR
    Dev Biol; 1985 Jan; 107(1):66-74. PubMed ID: 2578117
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Protein composition of the hyaline layer of sea urchin embryos and reaggregating cells.
    McCarthy RA; Spiegel M
    Cell Differ; 1983 Oct; 13(2):93-102. PubMed ID: 6661780
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Actin microfilaments play a critical role in endocytosis at the apical but not the basolateral surface of polarized epithelial cells.
    Gottlieb TA; Ivanov IE; Adesnik M; Sabatini DD
    J Cell Biol; 1993 Feb; 120(3):695-710. PubMed ID: 8381123
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Opposing microtubule- and actin-dependent forces in the development and maintenance of structural polarity in retinal photoreceptors.
    Madreperla SA; Adler R
    Dev Biol; 1989 Jan; 131(1):149-60. PubMed ID: 2642427
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Establishment and maintenance of a regionalized glycoprotein distribution during early mouse development.
    Pierce KE; Calarco PG
    Dev Biol; 1990 Jan; 137(1):56-67. PubMed ID: 2403948
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cytochalasin separates microtubule disassembly from loss of asymmetric morphology.
    Solomon F; Magendantz M
    J Cell Biol; 1981 Apr; 89(1):157-61. PubMed ID: 7014572
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.