Avoiding drug resistance through extended drug target interfaces: A case for stapled peptides
10.18632/oncotarget.8572
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sg-nus-scholar.10635-1799272024-04-18T02:17:13Z Avoiding drug resistance through extended drug target interfaces: A case for stapled peptides Wei, S.J Chee, S Yurlova, L Lane, D Verma, C Brown, C Ghadessy, F MEDICINE BIOLOGY (NU) nutlin peptide inhibitor protein inhibitor protein MDM2 protein p53 unclassified drug antineoplastic agent MDM2 protein, human peptide protein binding protein MDM2 protein p53 TP53 protein, human animal cell Article BHK cell line binding affinity controlled study drug protein binding drug resistance fibroblast fluorescence polarization immunoprecipitation in vitro study molecular model mouse neoplasm nonhuman phenotype point mutation protein binding protein expression protein function protein purification Western blotting wild type animal antagonists and inhibitors binding site cell line chemistry drug design drug effects gene expression regulation genetics genotype human metabolism molecular mimicry neoplasm pathology signal transduction structure activity relation Animals Antineoplastic Agents Binding Sites Cell Line Drug Design Drug Resistance, Neoplasm Gene Expression Regulation, Neoplastic Genotype Humans Mice Models, Molecular Molecular Mimicry Neoplasms Peptides Phenotype Point Mutation Protein Binding Proto-Oncogene Proteins c-mdm2 Signal Transduction Structure-Activity Relationship Tumor Suppressor Protein p53 10.18632/oncotarget.8572 Oncotarget 7 22 32232-32246 2020-10-26T05:08:17Z 2020-10-26T05:08:17Z 2016 Article Wei, S.J, Chee, S, Yurlova, L, Lane, D, Verma, C, Brown, C, Ghadessy, F (2016). Avoiding drug resistance through extended drug target interfaces: A case for stapled peptides. Oncotarget 7 (22) : 32232-32246. ScholarBank@NUS Repository. https://doi.org/10.18632/oncotarget.8572 19492553 https://scholarbank.nus.edu.sg/handle/10635/179927 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Unpaywall 20201031 |
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nutlin peptide inhibitor protein inhibitor protein MDM2 protein p53 unclassified drug antineoplastic agent MDM2 protein, human peptide protein binding protein MDM2 protein p53 TP53 protein, human animal cell Article BHK cell line binding affinity controlled study drug protein binding drug resistance fibroblast fluorescence polarization immunoprecipitation in vitro study molecular model mouse neoplasm nonhuman phenotype point mutation protein binding protein expression protein function protein purification Western blotting wild type animal antagonists and inhibitors binding site cell line chemistry drug design drug effects gene expression regulation genetics genotype human metabolism molecular mimicry neoplasm pathology signal transduction structure activity relation Animals Antineoplastic Agents Binding Sites Cell Line Drug Design Drug Resistance, Neoplasm Gene Expression Regulation, Neoplastic Genotype Humans Mice Models, Molecular Molecular Mimicry Neoplasms Peptides Phenotype Point Mutation Protein Binding Proto-Oncogene Proteins c-mdm2 Signal Transduction Structure-Activity Relationship Tumor Suppressor Protein p53 |
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nutlin peptide inhibitor protein inhibitor protein MDM2 protein p53 unclassified drug antineoplastic agent MDM2 protein, human peptide protein binding protein MDM2 protein p53 TP53 protein, human animal cell Article BHK cell line binding affinity controlled study drug protein binding drug resistance fibroblast fluorescence polarization immunoprecipitation in vitro study molecular model mouse neoplasm nonhuman phenotype point mutation protein binding protein expression protein function protein purification Western blotting wild type animal antagonists and inhibitors binding site cell line chemistry drug design drug effects gene expression regulation genetics genotype human metabolism molecular mimicry neoplasm pathology signal transduction structure activity relation Animals Antineoplastic Agents Binding Sites Cell Line Drug Design Drug Resistance, Neoplasm Gene Expression Regulation, Neoplastic Genotype Humans Mice Models, Molecular Molecular Mimicry Neoplasms Peptides Phenotype Point Mutation Protein Binding Proto-Oncogene Proteins c-mdm2 Signal Transduction Structure-Activity Relationship Tumor Suppressor Protein p53 Wei, S.J Chee, S Yurlova, L Lane, D Verma, C Brown, C Ghadessy, F Avoiding drug resistance through extended drug target interfaces: A case for stapled peptides |
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10.18632/oncotarget.8572 |
author2 |
MEDICINE |
author_facet |
MEDICINE Wei, S.J Chee, S Yurlova, L Lane, D Verma, C Brown, C Ghadessy, F |
format |
Article |
author |
Wei, S.J Chee, S Yurlova, L Lane, D Verma, C Brown, C Ghadessy, F |
author_sort |
Wei, S.J |
title |
Avoiding drug resistance through extended drug target interfaces: A case for stapled peptides |
title_short |
Avoiding drug resistance through extended drug target interfaces: A case for stapled peptides |
title_full |
Avoiding drug resistance through extended drug target interfaces: A case for stapled peptides |
title_fullStr |
Avoiding drug resistance through extended drug target interfaces: A case for stapled peptides |
title_full_unstemmed |
Avoiding drug resistance through extended drug target interfaces: A case for stapled peptides |
title_sort |
avoiding drug resistance through extended drug target interfaces: a case for stapled peptides |
publishDate |
2020 |
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https://scholarbank.nus.edu.sg/handle/10635/179927 |
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1800914573707968512 |