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Volumn 1249, Issue , 2015, Pages 111-120
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A high-throughput cellular assay to quantify the p53- degradation activity of E6 from different human papillomavirus types
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Author keywords
Cancer; Cell based assay; E6; High risk; High throughput; Low risk; Luciferase; Oncogenesis; P53; Papillomavirus
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Indexed keywords
FIREFLY LUCIFERASE;
HYBRID PROTEIN;
PROTEASOME;
PROTEIN E6;
PROTEIN P53;
RENILLA LUCIFERIN 2 MONOOXYGENASE;
E6 PROTEIN, HUMAN PAPILLOMAVIRUS TYPE 16;
LUCIFERASE;
ONCOPROTEIN;
REPRESSOR PROTEIN;
ARTICLE;
CELL ASSAY;
CELL FUSION;
CONCENTRATION RESPONSE;
EC50;
ENZYME ACTIVITY;
EXPRESSION VECTOR;
GENETIC TRANSFECTION;
HIGH THROUGHPUT CELLULAR ASSAY;
HUMAN;
HUMAN CELL;
HUMAN PAPILLOMAVIRUS TYPE 16;
INFECTION RISK;
LUCIFERASE ASSAY;
PRIORITY JOURNAL;
PROTEIN DEGRADATION;
PROTEIN DETERMINATION;
QUANTITATIVE ASSAY;
RISK ASSESSMENT;
RISK FACTOR;
SENSITIVITY ANALYSIS;
STEADY STATE;
UTERINE CERVIX CARCINOMA;
WART VIRUS;
GENE VECTOR;
HIGH THROUGHPUT SCREENING;
METABOLISM;
PLASMID;
PROCEDURES;
TUMOR CELL LINE;
HUMAN PAPILLOMAVIRUS;
HUMAN PAPILLOMAVIRUS TYPES;
PAPILLOMAVIRIDAE;
RENILLA LUCIFERASE;
CELL LINE, TUMOR;
GENETIC VECTORS;
HIGH-THROUGHPUT SCREENING ASSAYS;
HUMANS;
LUCIFERASES;
ONCOGENE PROTEINS, VIRAL;
PLASMIDS;
PROTEOLYSIS;
REPRESSOR PROTEINS;
TRANSFECTION;
TUMOR SUPPRESSOR PROTEIN P53;
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EID: 84958608703
PISSN: 10643745
EISSN: None
Source Type: Book Series
DOI: 10.1007/978-1-4939-2013-6_8 Document Type: Article |
Times cited : (5)
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References (10)
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