colchicine/sarkom

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Effects of cytochalasin B and colchicine on the motility and growth of Yoshida sarcoma cells in vitro.

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The effects of cytochalasin B (CB) and colchicine on the motility and growth of cultured Yoshida sarcoma cells are studied by cinematographic methods. CB was found to reduce the average locomotory rate of motile Yoshida sarcoma cells and to enhance the frequency of non-motile cells. On the other

The binding of colchicine by sarcoma 180 cells.

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Studies on effects of colchicine derivatives upon Yoshida sarcoma cells.

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Studies on colchicine derivatives; toxicity in mice and effects on mouse sarcoma 180.

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Steatorrhoea and jejunal reticulum cell sarcoma occurring in a patient on long-term colchicine therapy for gout.

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[Effect of compounds having unsaturated seven membered ring structure on Yoshida sarcoma. IV. Appendix: with two cases of clinical application of colchicine-derivatives].

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Damage induced in sarcoma 37 with chemical agents. V. Derivatives of colchicine and isocolchicine.

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Damage induced in sarcoma 37 with chemical agents. III. Colchicine derivatives related to trimethylcolchicinic acid and to colchinol.

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Phase II study of CI-980 (NSC 635370) in patients with previously treated advanced soft-tissue sarcomas.

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Doxorubicin and ifosfamide are the two most active agents in the treatment of soft-tissue sarcomas. Patients whose tumors have failed these two drugs have very limited systemic therapy options. It is, therefore, important to identify newer drugs with activity against this disease. CI-980 is a

Requirement for cell division for initiation of transcription of Rous sarcoma virus RNA.

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Stationary chicken embryo fibroblasts exposed to Rous sarcoma virus (RSV) did not synthesize virus RNA until after division of the infected cells. Initiation of RNA transcription after cell division resulted in transcription of the entire viral genome and was followed shortly thereafter by

Induced multidrug-resistance in murine sarcoma 180 cells grown in vitro and in vivo and associated changes in expression of multidrug-resistance DNA-sequences and membrane glycoproteins.

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The aim of this investigation was to analyze the resistance to doxorubicin and daunorubicin of murine sarcoma 180 cells grown in vitro (monolayer) and in vivo (ascites form). The colchicine-resistant CHO cells were used as controls. A multidrug-resistant phenotype was found in all investigated cell

Rous sarcoma virus infection of synchronized cells establishes provirus integration during S-phase DNA synthesis prior to cellular division.

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Synchronized chicken embryo fibroblasts, prepared by addition of serum to stationary cells arrested in Go, were exposed to the Prague strain of Rous sarcoma virus. At different times during the cell cycle, high molecular weight DNA was prepared from infected cells and examined for the presence of

Independent expression of avian sarcoma virus in doubly infected chicken embryo fibroblasts.

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Infection of a chicken cell with avian sarcoma virus requires division of the infected cell before synthesis of infectious progeny is initiated. This requirement for a cell division for the complete expression of avian sarcoma virus has been examined further with chicken embryo fibroblasts infected

[Studies on the tissue culture of murine sarcoma (Dunn sarcoma)--a fix cell line established in vitro (DSK) and its cytokinetic findings (author's transl)].

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Dunn osteosarcoma, transplanted successively from the original spontaneous murine osteosarcoma, was cultured for generations and serial changes of cultured cells were observed morphologically and also from the view points of chromosomes and cytokinetics. 1) In the early generations of subculture,

Pleiotropic phenotype of cultured murine cells resistant to maytansine, vincristine, colchicine, and adriamycin.

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A noncloned subline of 3T3FL cells was developed that was resistant to the toxicity of the ansamycin alkaloid maytansine. Culture of 3T3FL cells with serially increasing concentrations of maytansine resulted in a cell line resistant to maytansine at concentrations 118-fold higher than concentrations

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