scholarly article | Q13442814 |
P2093 | author name string | Deppert W | |
Klockmann U | |||
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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 | Q25938983 | ||
The protein encoded by the transforming gene of avian sarcoma virus (pp60src) and a homologous protein in normal cells (pp60proto-src) are associated with the plasma membrane | Q28575831 | ||
A Film Detection Method for Tritium-Labelled Proteins and Nucleic Acids in Polyacrylamide Gels | Q29547782 | ||
Nuclear matrix. Isolation and characterization of a framework structure from rat liver nuclei | Q30424642 | ||
Antigenic and immunogenic characteristics of nuclear and membrane-associated simian virus 40 tumor antigen. | Q33915246 | ||
Monoclonal antibodies against simian virus 40 T antigens: evidence for distinct sublcasses of large T antigen and for similarities among nonviral T antigens | Q33920832 | ||
Two forms of simian-virus-40-specific T-antigen in abortive and lytic infection | Q34996059 | ||
Simian virus to (SV40) tumor-specific proteins in nucleus and plasma membrane of HeLa cells infected by adenovirus 2-SV40 hybrid virus Ad2+ND2 | Q35012456 | ||
Virus-specific proteins in the plasma membrane of cells lytically infected or transformed by pol-oma virus | Q35058806 | ||
Detection and characterization of multiple forms of simian virus 40 large T antigen | Q35235163 | ||
Complex of simian virus 40 large-T antigen and host 53,000-molecular-weight protein in monkey cells | Q35235746 | ||
Complex of simian virus 40 large tumor antigen and 48,000-dalton host tumor antigen | Q35299950 | ||
DETECTION OF SPECIFIC ANTIGEN IN SV40-TRANSFORMED CELLS BY IMMUNOFLUORESCENCE | Q36266598 | ||
Carboxy terminus of polyoma middle-sized tumor antigen is required for attachment to membranes, associated protein kinase activities, and cell transformation | Q36298676 | ||
Association of the src gene product of Rous sarcoma virus with cytoskeletal structures of chicken embryo fibroblasts | Q36393988 | ||
Adhesion plaques of Rous sarcoma virus-transformed cells contain the src gene product | Q36394145 | ||
Subcellular Localization of Simian Virus 40 Large Tumor Antigen | Q36498106 | ||
Preparation of syngeneic tumor regressor serum reactive with the unique determinants of the Abelson murine leukemia virus-encoded P120 protein at the cell surface | Q36502242 | ||
Association of pp60src and src protein kinase activity with the plasma membrane of nonpermissive and permissive avian sarcoma virus-infected cells | Q36508814 | ||
Measurements of the molecular size of the simian virus 40 large T antigen | Q36522386 | ||
Simian virus 40 gene A function and maintenance of transformation | Q36532450 | ||
Regulation of tumor antigen synthesis by simain virus 40 gene A | Q36537613 | ||
Time-dependent maturation of the simian virus 40 large T antigen-p53 complex studied by using monoclonal antibodies | Q36926635 | ||
Different forms of simian virus 40 large tumor antigen varying in their affinities for DNA | Q36940094 | ||
Polyoma Virus Middle T Antigen: Relationship to Cell Membranes and Apparent Lack of ATP-Binding Activity | Q36975407 | ||
Simian virus 40 tumor-specific proteins: subcellular distribution and metabolic stability in HeLa cells infected with nondefective adenovirus type 2-simian virus 40 hybrid viruses | Q37503557 | ||
Simian virus 40 T- and U-antigens: immunological characterization and localization in different nuclear subfractions of simian virus 40-transformed cells | Q39538638 | ||
Cell surface location of simian virus 40-specific proteins on HeLa cells infected with adenovirus type 2-simian virus 40 hybrid viruses Ad2+ND1 and Ad2+ND2 | Q39564514 | ||
Cellular location of viral transforming proteins | Q40122488 | ||
Effect of alkylation on the physical properties of simian virus 40 T-antigen species | Q40218996 | ||
Polyoma virus-specific 55K protein isolated from plasma membrane of productively infected cells is virus-codedand important for cell transformation | Q40256089 | ||
Localization of the ASV src gene product to the plasma membrane of transformed cells by electron microscopic immunocytochemistry | Q40273384 | ||
Association of a murine 53,000-dalton phosphoprotein with simian virus 40 large-T antigen in transformed cells | Q40307090 | ||
Simian virus 40 T-antigen-related cell surface antigen: serological demonstration on simian virus 40-transformed monolayer cells in situ | Q40307810 | ||
Surface modulation in cell recognition and cell growth | Q40490719 | ||
Subclasses of simian virus 40 large T antigen: differential binding of two subclasses of T antigen from productively infected cells to viral and cellular DNA | Q41311773 | ||
The outer boundary of the cytoskeleton: a lamina derived from plasma membrane proteins | Q41963121 | ||
Two polyoma virus gene functions involved in the expression of the transformed phenotype in FR 3T3 rat cells II. The presence of the 56K middle-T protein in the cell membrane is not sufficient for maintenance | Q42826406 | ||
Two polyoma virus gene functions involved in the expression of the transformed phenotype in FR 3T3 rat cells I. Localization of a transformation maintenance function in the proximal half of the large T coding region | Q42826415 | ||
Acylation: A new post‐translational modification specific for plasma membrane‐associated simian virus 40 large T‐antigen | Q43540621 | ||
SV40-transformed cells express SV40 T antigen-related antigens on the cell surface | Q43749432 | ||
Covalent binding of fatty acid to the transferrin receptor in cultured human cells | Q44051513 | ||
Evidence that the src gene product of rous sarcoma virus is membrane associated | Q44731356 | ||
Changes in amino-terminal sequences of pp60src lead to decreased membrane association and decreased in vivo tumorigenicity | Q45077792 | ||
Cell surface binding affinity of simian virus and 40 T-antigen | Q45792984 | ||
Acylated simian virus 40-specific proteins in the plasma membrane of HeLa cells infected with adenovirus 2-simian virus 40 hybrid virus Ad2+ND2. | Q45793937 | ||
The transforming proteins of Rous sarcoma virus, Harvey sarcoma virus and Abelson virus contain tightly bound lipid | Q45798971 | ||
Transformation of rat cells by an altered polyoma virus genome expressing only the middle-T protein | Q45801875 | ||
Domains of simian virus 40 large T-antigen exposed on the cell surface | Q45805091 | ||
Early changes in the distribution and organization of microfilament proteins during cell transformation | Q53571722 | ||
Localization of the src gene product of the Harvey strain of MSV to plasma membrane of transformed cells by electron microscopic immunocytochemistry | Q53577737 | ||
Immunological identification of two adenovirus 2-induced early proteins possibly involved in cell transformation | Q59064234 | ||
Actin-containing matrix associated with the plasma membrane of murine tumour and lymphoid cells | Q59064648 | ||
Proteolipids | Q70174032 | ||
Relationship of oligomerization to enzymatic and DNA-binding properties of the SV40 large T antigen | Q70567810 | ||
A new cell surface, detergent-insoluble glycoprotein matrix of human and hamster fibroblasts. The role of disulfide bonds in stabilization of the matrix | Q70797668 | ||
Fatty acid acylation of proteins in cultured cells | Q71364293 | ||
Different structural systems of the nucleus are targets for SV40 large T antigen | Q72388899 | ||
Acylation of virol. spike glycoproteins: A feature of enveloped RNA viruses | Q72924789 | ||
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | SV40 | Q734305 |
P304 | page(s) | 1151-1157 | |
P577 | publication date | 1983-01-01 | |
P1433 | published in | The EMBO Journal | Q1278554 |
P1476 | title | Acylated simian virus 40 large T-antigen: a new subclass associated with a detergent-resistant lamina of the plasma membrane | |
P478 | volume | 2 |
Q36910624 | Absence of a structural basis for intracellular recognition and differential localization of nuclear and plasma membrane-associated forms of simian virus 40 large tumor antigen. |
Q38641081 | Acylation of viral and eukaryotic proteins |
Q35585923 | Ankyrin is fatty acid acylated in erythrocytes |
Q40670990 | Ankyrin-bound fatty acid turns over rapidly at the erythrocyte plasma membrane |
Q40670377 | Evidence for free and metabolically stable p53 protein in nuclear subfractions of simian virus 40-transformed cells |
Q40124939 | Evidence for transmembrane orientation of acylated simian virus 40 large T antigen |
Q42143873 | Fatty acid acylation at the single cysteine residue in the cytoplasmic domain of the glycoprotein of vesicular-stomatitis virus |
Q38729752 | Fatty acylation of proteins |
Q41566268 | Identification of acyl donors and acceptor proteins for fatty acid acylation in BHK cells infected with Semliki Forest virus. |
Q41391683 | In vivo acylation of Dictyostelium actin with palmitic acid. |
Q35849175 | Initial characterization of the membrane-associated form of ICP4 of herpes simplex virus type 1 |
Q36831658 | Linker insertion mutants of simian virus 40 large T antigen that show trans-dominant interference with wild-type large T antigen map to multiple sites within the T-antigen gene |
Q36946529 | Membrane Interactions of Simian Virus 40 Large T-Antigen: Influence of Protein Sequences and Fatty Acid Acylation |
Q39578212 | Modification of proteins with covalent lipids |
Q33928962 | N protein is the predominant antigen recognized by vesicular stomatitis virus-specific cytotoxic T cells |
Q40132757 | Oligomerization and origin DNA-binding activity of simian virus 40 large T antigen |
Q40116855 | Only a minor fraction of plasma membrane-associated large T antigen in simian virus 40-transformed mouse tumor cells (mKSA) is exposed on the cell surface |
Q36897404 | Plasma membrane orientation of simian virus 40 T antigen in three transformed cell lines mapped with monoclonal antibodies |
Q36889566 | Posttranslational processing of the Epstein-Barr virus-encoded p63/LMP protein |
Q41456343 | Preparation of nuclear matrices from cultured cells: subfractionation of nuclei in situ |
Q36797816 | Properties of the DNA-binding domain of the simian virus 40 large T antigen |
Q33928759 | Regulation of SV40 DNA replication by phosphorylation of T antigen |
Q41396801 | SV40 T antigen and the exocytotic pathway |
Q40132622 | Sequence and structural organization of murine cytomegalovirus immediate-early gene 1. |
Q36832198 | Simian virus 40 host range/helper function mutations cause multiple defects in viral late gene expression |
Q36855375 | Simian virus 40 origin DNA-binding domain on large T antigen. |
Q41391599 | Studies on the attachment of myristic and palmitic acid to cell proteins in human squamous carcinoma cell lines: evidence for two pathways |
Q42269767 | Subcellular localisation of the middle and large T-antigens of polyoma virus |
Q33932011 | The abnormal location of cytoplasmic SV40 large T is not caused by failure to bind to DNA or to p53. |
Q36920447 | The cellular secretory pathway is not utilized for biosynthesis, modification, or intracellular transport of the simian virus 40 large tumor antigen |
Q39655733 | The covalent modification of eukaryotic proteins with lipid |
Q34330457 | The cyclin-dependent kinase inhibitor roscovitine inhibits the transactivating activity and alters the posttranslational modification of herpes simplex virus type 1 ICP0. |
Q42567525 | The kinase activity of SV40 large T antigen is mediated by a cellular kinase |
Q41527124 | The transfer of myristic and other fatty acids on lipid and viral protein acceptors in cultured cells infected with Semliki Forest and influenza virus |