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glucosamine/сарком
Веза се чува у привремену меморију
Страна 1 од 59 резултати
Effect of glucosamine on phenotype mixing of vesicular stomatitis virus with avian sarcoma virus.
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The effect of glucosamine on phenotypic mixing between vesicular stomatitis virus (VSV) and avian sarcoma virus (ASV) was studied. Phenotypic mixing decreased with increase in glucosamine concentration, and, in the presence of 20 mM glucosamine, was no longer detectable. In the presence of 20 mM
Effect of glucosamine on virus production and antigen expression in avian sarcoma virus-transformed cells.
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Treatment by glucosamine of avian sarcoma virus-transformed chicken embryo fibroblast (CEF) cells completely inhibited the formation of progeny-transforming virus particles. Such cells, however, could continue to synthesize non-infectious physical particles containing both viral RNA and the enzyme
Inhibition of avian sarcoma virus replication by glucosamine.
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Viral glycoprotein synthesis under conditions of glucosamine block in cells transformed by avian sarcoma viruses.
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Inhibition of avian sarcoma virus replication by glucosamine: a specific effect on the synthesis and processing of viral proteins.
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The effect of D-glucosamine hydrochloride and related compounds on tissue cultures of the solid form of mouse sarcoma 37.
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The effect of D-glucosamine on the adenine and uridine nucleotides of sarcoma 180 ascites tumor cells.
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A syngeneic monoclonal antibody to murine Meth-A sarcoma (HepSS-1) recognizes heparan sulfate glycosaminoglycan (HS-GAG): cell density and transformation dependent alteration in cell surface HS-GAG defined by HepSS-1.
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We have isolated a syngeneic monoclonal antibody (HepSS-1) reactive to a murine methylcholanthrene-induced fibrosarcoma, Meth-A. HepSS-1 also bound to a wide variety of established and fresh normal cells derived from not only mice but also other species such as human, monkey, rat, hamster, and
In vivo antiviral activity of D-glucosamine.
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Intraperitoneal treatments with D-glucosamine, an inhibitor of the glycosylation of the viral envelope, decreased the growth rate of tumors induced in quails or in chicks by Rous sarcoma virus and increased the survival of mice inoculated with human influenza virus.
Characterization of rat hepatoma glucosamine 6-phosphate synthase and its relation to liver and fetal forms.
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Glucosamine 6-phosphate synthase (EC 5.3.1.19) purified from various rat tissues by a procedure involving chromatography on diethylaminoethyl Sephadex and hydroxylapatite were characterized by means of isoelectric focusing. The non-hepatic isozyme, previously reported to be present in Yoshida
Detection of type A oncornavirus-like structures in chicken embryo cells after infection with Rous sarcoma virus.
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Electron microscopy examination of Rous sarcoma virus-transformed chicken embryo cells revealed membrane-free nucleoids resembling type A oncornavirus. These particles were not detected in noninfected cells, nor did they accumulate in excess under conditions of glucosamine block in virus-transformed
T- and B-cell-independent activation of syngeneic macrophages by murine sarcoma cells.
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Mouse peritoneal macrophages were achieved by cocultivation with syngeneic sarcoma cells. The tumor cells died progressively during the cocultivation, leaving highly activated marcophages. Because of great changes in macrophage morphology during the activation, special efforts were made to identify
Investigations on the aminoacid content of tumor associated antigens of rat sarcoma cells induced by virus.
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In our previous work (Alexandrov et al., 1996) was reported that the rat sarcoma cells induced by SR-RSV express two tumor associated antigens (TAA). The one TAA has a molecular weight of 52 kD and is detected by the help of a monoclonal antibody 2C2 only on the outer side of the plasma membrane of
Glycopeptides derived from individual membrane glycoproteins from control and Rous sarcoma virus-transformed hamster fibroblasts.
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The membrane glycoproteins from control (BHK21/C13) and Rous sarcoma virus-transformed (C13/B4) baby hamster kidney cells grown in medium containing [14C]- or D-[3H]glucosamine have been separated into two distinct classes: a phenol-soluble fraction and an aqueous fraction. The membrane
Immunoprecipitation of membrane proteins of cultured human sarcoma cells.
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Human sarcoma associated antigens (HSAA) have previously been identified by indirect immune fluorescence in human sarcoma cells in culture using sera from patients bearing different types of sarcoma. To further characterize these HSAA, surface proteins of cultured cells were labeled with 125Iodine,
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