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  1. 3601
    por Kaneko, M., Horikoshi, J.
    Publicado 1987
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    Topoisomerase inhibitors suppressed lithocholic acid-induced promotion of transformation in BALB/3T3.
  2. 3602
    “…Thus, lhen plasmin was present 3T3 cells did not become transformed, but expresses transformation-like features. …”
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    Plasminogen activation transforms the morphology of quiescent 3T3 cell monolayers and initiates growth.
  3. 3603
    Publicado 1998
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    Selective activation of oncogenic Ha-ras-induced apoptosis in NIH/3T3 cells
  4. 3604
    Publicado 1975
    “…A protein component of membranes isolated from 3T3 mouse fibroblasts and HeLa cells has been identified as actin by peptide mapping. …”
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    Actin associated with membranes from 3T3 mouse fibroblast and HeLa cells
  5. 3605
    Publicado 1976
    “…Freshly plated 3T3 cells send out radial projections or filopodia. …”
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    Filopodia of spreading 3T3 cells. Do they have a substrate-exploring function?
  6. 3606
    por Tupper, JT, Zorgniotti, F
    Publicado 1977
    “…Total Ca content and that fraction of Ca sensitive to removal by the chelator ethylene glycol-bis(β-aminoethyl ether)N,N,N',N'-tetraacetate (EGTA) have been investigated in the mouse 3T3 cell as a function of growth stage, transformation with SV40 virus, and serum levels of the media. …”
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    Calcium content and distribution as a function of growth and transformation in the mouse 3T3 cell
  7. 3607
    Publicado 1983
    “…The results presented here show that disruption of the microtubule network acts synergistically with cAMP-elevating agents to stimulate the entry into DNA synthesis of 3T3 cells. Antimicrotubule agents and increased cAMP levels require an additional growth-promoting factor for inducing initiation of DNA synthesis; such requirement can be furnished by insulin, vasopressin, epidermal growth factor, platelet-derived growth factor, or fibroblast-derived growth factor. …”
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    Interplay of cyclic AMP and microtubules in modulating the initiation of DNA synthesis in 3T3 cells
  8. 3608
    Publicado 1987
    “…Nonmotile, confluent Swiss 3T3 cells did not show any detectable polarity of cell shape, or distribution of nuclei, endosomes, or mitochondria. …”
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    Five-parameter fluorescence imaging: wound healing of living Swiss 3T3 cells
  9. 3609
    Publicado 1988
    “…Nucleocytoplasmic transport of fluorescent-labeled macromolecules was investigated in transformed and nontransformed 3T3 fibroblasts. Insulin and epidermal growth factor enhanced transport three-fold after 1-2-h incubation with nontransformed adhering fibroblasts; no enhancement of transport was observed for spherical unattached fibroblasts. …”
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    Nuclear transport in 3T3 fibroblasts: effects of growth factors, transformation, and cell shape
  10. 3610
    “…The isolation of clonal lines of murine sarcoma virus-transformed, non-producer BALB/3T3 cells has provided a model system for determining whether RNA tumor virus-transformed cells possess virus-specific transplantation antigens. …”
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    ANTIGENIC PROPERTIES OF MURINE SARCOMA VIRUS-TRANSFORMED BALB/3T3 NONPRODUCER CELLS
  11. 3611
    “…A Ha-ras transformant '7-4', derived from mouse NIH/3T3 fibroblasts, was used to study the relationship between overexpression of activated Ha-ras and cell apoptosis. …”
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    Selective activation of oncogenic Ha-ras-induced apoptosis in NIH/3T3 cells.
  12. 3612
    “…These studies suggest that a pathway for PI(3,4,5)P(3) synthesis downstream of a class III phosphoinositide 3-kinase evolved before the appearance of class I phosphoinositide 3-kinases.…”
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    A novel phosphatidylinositol(3,4,5)P(3) pathway in fission yeast
  13. 3613
    Publicado 1983
    “…C3a liberated from C3 by treatment with C3 convertase (or by trypsin) induced aggregation of gel-filtered human platelets and stimulated serotonin release. …”
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    Human platelet activation by C3a and C3a des-arg
  14. 3614
    Publicado 1985
    “…A new cluster of complement component genes, including C4BP, C3bR, and FH, is described. Family segregation data indicate that FH is linked to the genes for C4-bp and C4bR, previously reported to be linked and to maintain linkage disequilibrium. …”
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    Human genes for three complement components that regulate the activation of C3 are tightly linked
  15. 3615
    Publicado 1986
    “…A bank of gonococcal DNA was constructed in the lambda gt11 expression vector. immunological screening of the bank resulted in the isolation of a clone that contains the structural gene of protein III. In addition, several clones reactive with mAbs specific for the H8 antigen were isolated. …”
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    Cloning of the structural genes of three H8 antigens and of protein III of Neisseria gonorrhoeae
  16. 3616
    “…The effect of NO(3) (−) on intracellular pH (pH(i)) was assessed microfluorimetrically in mammalian cells in culture. …”
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    NO(3) (−)-induced pH Changes in Mammalian Cells : Evidence for an NO(3)(−)-H(+) Cotransporter
  17. 3617
    Publicado 1992
    “…Approximately 23% of the glycolytic enzyme aldolase in the perinuclear region of Swiss 3T3 cells is immobile as measured by FRAP. Previous studies suggest that the immobile fraction may be associated with the actin cytoskeleton (Pagliaro, L. and D. …”
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    2-Deoxyglucose and cytochalasin D modulate aldolase mobility in living 3T3 cells
  18. 3618
    Publicado 1991
    “…3T3-L1 fibroblasts were induced to differentiate to 3T3-L1 adipocytes by dexamethasone, isobutyl-methylxanthine, and insulin. …”
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    Alteration of proteoglycan metabolism during the differentiation of 3T3- L1 fibroblasts into adipocytes
  19. 3619
    “…The ruthenium(III) complex Hlnd trans-[RuCl(4),(ind)(2)], with two trans-standing indazole (ind) ligands bound to ruthenium via nitrogen, shows remarkable activity in different tumor models in vitro and in vivo. …”
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    Solvolysis of the Tumor-Inhibiting Ru(III)-Complex trans-Tetrachlorobis(Indazole)Ruthenate(III)
  20. 3620
    “…These contigs correspond to seven plasmids: pSci1 to pSci6, with sizes ranging from 12.9 to 35.3 kbp and pSciA of 7.8 kbp. Plasmids pSci were detected as multiple copies in strain GII3-3X. …”
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    The abundant extrachromosomal DNA content of the Spiroplasma citri GII3-3X genome
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