LARGE-TUMOR-ANTIGEN
p300 family members associate with the carboxyl terminus of simian virus 40 large tumor antigen.
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Complex formation between the lymphotropic papovavirus large tumor antigen and the tumor suppressor protein p53.
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CD4+ T Lymphocytes Are Critical Mediators of Tumor Immunity to Simian Virus 40 Large Tumor Antigen Induced by Vaccination with Plasmid DNA
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The block of adipocyte differentiation by a C-terminally truncated, but not by full-length, simian virus 40 large tumor antigen is dependent on an intact retinoblastoma susceptibility protein family binding domain.
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The large tumor antigen of simian virus 40 encodes at least two distinct transforming functions.
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Role of the Innate Immune Response and Tumor Immunity Associated with Simian Virus 40 Large Tumor Antigen
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Intestinal Hyperplasia Induced by Simian Virus 40 Large Tumor Antigen Requires E2F2
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Subcellular Localization of Simian Virus 40 Large Tumor Antigen
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The replication functions of polyomavirus large tumor antigen are regulated by phosphorylation.
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Different forms of simian virus 40 large tumor antigen varying in their affinities for DNA.
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Association of p53 binding and immortalization of primary C57BL/6 mouse embryo fibroblasts by using simian virus 40 T-antigen mutants bearing internal overlapping deletion mutations.
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Common and unique features of T antigens encoded by the polyomavirus group.
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Phenotype-specific phosphorylation of simian virus 40 tsA mutant large T antigens in tsA N-type and A-type transformants.
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Mutual functional antagonism of the simian virus 40 T antigen and the hepatitis B virus trans activator.
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Site-directed mutagenesis of the simian virus 40 large T-antigen gene: replication-defective amino acid substitution mutants that retain the ability to induce morphological transformation.
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Three domains in the simian virus 40 core origin orchestrate the binding, melting, and DNA helicase activities of T antigen.
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A DNA replication-positive mutant of simian virus 40 that is defective for transformation and the production of infectious virions.
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Mapping of helicase and helicase substrate-binding domains on simian virus 40 large T antigen.
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Monoclonal antibodies as probes for a function of large T antigen during the elongation process of simian virus 40 DNA replication.
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Differential induction of structural changes in the simian virus 40 origin of replication by T antigen.
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