http://www.cnr.it/ontology/cnr/individuo/parolaChiave/49289
drug resistance
- Label
- drug resistance (literal)
- Membro di
- Parole chiave di "Arylthiopyrrole (AThP) Derivatives as Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors: Synthesis, Structure-Activity Relationships, and Docking Studies (Part 2)." (Insieme di parole chiave)
- Keywords of "Prevalence of mutations and determinants of genotypic resistance to etravirine (TMC125) in a large Italian resistance database (ARCA)" (Insieme di parole chiave)
- Parole chiave di "Enhancing therapeutic efficacy by targeting non-oncogene addicted cells with combinations of signal transduction inhibitors and chemotherapy." (Insieme di parole chiave)
- Parole chiave di "Substrate-Induced Stable Enzyme-Inhibitor Complex Formation Allows Tight Binding of Novel 2-Aminopyrimidin-4(3H)-ones to Drug-Resistant HIV-1 Reverse Transcriptase Mutants." (Insieme di parole chiave)
- Parole chiave di "Drug treatment of cancer cell lines: a way to select for cancer stem cells?" (Insieme di parole chiave)
- Parole chiave di "Design, synthesis, biological evaluation, and molecular modeling studies of TIBO-like cyclic sulfones as non-nucleoside HIV-1 reverse transcriptase inhibitors." (Insieme di parole chiave)
- Parole chiave di "Indolyl aryl sulphones as HIV-1 non-nucleoside reverse transcriptase inhibitors: synthesis, biological evaluation and binding mode studies of new derivatives at indole-2-carboxamide." (Insieme di parole chiave)
- Parole chiave di "Arylthiopyrrole (ATP) Derivatives as Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors." (Insieme di parole chiave)
- Parole chiave di "Design, molecular modeling, synthesis, and anti-HIV-1 activity of new indolyl aryl sulfones. Novel derivatives of the indole-2-carboxamide." (Insieme di parole chiave)
- Keywords of "Model for the Chemotherapy of HIV with Antigenic Variation" (Insieme di parole chiave)
- Keywords of "Non-nucleoside HIV-1 reverse transcriptase inhibitors di-halo-indolyl aryl sulfones achieve tight binding to drug-resistant mutants by targeting the enzyme-substrate complex." (Insieme di parole chiave)
- Keywords of "Slow binding-tight binding interaction between benzimidazol-2-one inhibitors and HIV-1 reverse transcriptase containing the lysine 103 to asparagine mutation." (Insieme di parole chiave)
- Parole chiave di "Specific targeting highly conserved residues in the HIV-1 reverse transcriptase primer grip region. Design, synthesis, and biological evaluation of novel, potent, and broad spectrum NNRTIs with antiviral activity." (Insieme di parole chiave)
- Parole chiave di "Targeting the leukemic stem cell: the Holy Grail of leukemia therapy." (Insieme di parole chiave)
- Parole chiave di "Novel N1-substituted 1,3-dihydro-2H-benzimidazol-2-ones as potent non-nucleoside reverse transcriptase inhibitors." (Insieme di parole chiave)
- Keywords of "The effects of prolonged treatment with zidovudine, lamivudine, and abacavir on a T-lymphoblastoid cell line." (Insieme di parole chiave)
- Parole chiave di "A multidisciplinary approach for the identification of novel HIV-1 non-nucleoside reverse transcriptase inhibitors: S-DABOCs and DAVPs." (Insieme di parole chiave)
- Parole chiave di "The Raf/MEK/ERK pathway can govern drug resistance, apoptosis and sensitivity to targeted therapy." (Insieme di parole chiave)
- Keywords of "Towards novel S-DABOC inhibitors: Synthesis, biological investigation, and molecular modeling studies." (Insieme di parole chiave)
- Parole chiave di "Induction of nuclear receptors and drug resistance in the brain microvascular endothelial cells treated with antiepileptic drugs." (Insieme di parole chiave)
- Keywords of "Nucleoside reverse transcriptase inhibitor resistance mutations associated with first-line stavudine-containing antiretroviral therapy: Programmatic implications for countries phasing out stavudine" (Insieme di parole chiave)
- Keywords of "Efficacy of ST1968 (namitecan) on a topotecan-resistant squamous cell carcinoma." (Insieme di parole chiave)
- Keywords of "Drug resistance mutations in the nucleotide binding pocket of human immunodeficiency virus type 1 reverse transcriptase differentially affect the phosphorolysis-dependent primer unblocking activity in the presence of stavudine and zidovudine and its inhib" (Insieme di parole chiave)
- Keywords of "Novel 1-[2-(diarylmethoxy)ethyl]-2-methyl-5-nitroimidazoles as HIV-1 non-nucleoside reverse transcriptase inhibitors. A structure-activity relationship investigation." (Insieme di parole chiave)
- Parole chiave di "Synthesis and biological investigation of S-aryl-S-DABO derivatives as HIV-1 inhibitors." (Insieme di parole chiave)
- Parole chiave di "Dominant roles of the Raf/MEK/ERK pathway in cell cycle progression, prevention of apoptosis and sensitivity to chemotherapeutic drugs." (Insieme di parole chiave)
- Keywords of "The cyclin-dependent kinase inhibitor roscovitine and the nucleoside analog sangivamycin induce apoptosis in caspase-3 deficient breast cancer cells independent of caspase mediated P-glycoprotein cleavage: implications for therapy of drug resistant breast" (Insieme di parole chiave)
- Keywords of "5-Alkyl-6-benzyl-2-(2-oxo-2-phenylethylsulfanyl)pyrimidin-4(3H)-ones, a series of anti-HIV-1 agents of the dihydro-alkoxy-benzyl-oxopyrimidine family with peculiar structure-activity relationship profile." (Insieme di parole chiave)
- Parole chiave di "High potency of indolyl aryl sulfone nonnucleoside inhibitors towards drug-resistant human immunodeficiency virus type 1 reverse transcriptase mutants is due to selective targeting of different mechanistic forms of the enzyme." (Insieme di parole chiave)
- Keywords of "Parallel solution-phase and microwave-assisted synthesis of new S-DABO derivatives endowed with subnanomolar anti-HIV-1 activity." (Insieme di parole chiave)
- Keywords of "Selective targeting of the HIV-1 reverse transcriptase catalytic complex through interaction with the" (Insieme di parole chiave)
- Keywords of "Non apoptotic programmed cell death induced by a phosphine copper(I) complex as a new tool for overcoming cisplatin and multi drug resistance" (Insieme di parole chiave)
- Parole chiave di "Resistance of Schistosoma mansoni to praziquantel: is there a problem?" (Insieme di parole chiave)
- Value
- drug resistance (literal)
Incoming links:
- Ha membro
- Keywords of "Non apoptotic programmed cell death induced by a phosphine copper(I) complex as a new tool for overcoming cisplatin and multi drug resistance" (Insieme di parole chiave)
- Parole chiave di "Synthesis and biological investigation of S-aryl-S-DABO derivatives as HIV-1 inhibitors." (Insieme di parole chiave)
- Keywords of "Drug resistance mutations in the nucleotide binding pocket of human immunodeficiency virus type 1 reverse transcriptase differentially affect the phosphorolysis-dependent primer unblocking activity in the presence of stavudine and zidovudine and its inhib" (Insieme di parole chiave)
- Keywords of "Novel 1-[2-(diarylmethoxy)ethyl]-2-methyl-5-nitroimidazoles as HIV-1 non-nucleoside reverse transcriptase inhibitors. A structure-activity relationship investigation." (Insieme di parole chiave)
- Parole chiave di "Design, molecular modeling, synthesis, and anti-HIV-1 activity of new indolyl aryl sulfones. Novel derivatives of the indole-2-carboxamide." (Insieme di parole chiave)
- Parole chiave di "Targeting the leukemic stem cell: the Holy Grail of leukemia therapy." (Insieme di parole chiave)
- Keywords of "Non-nucleoside HIV-1 reverse transcriptase inhibitors di-halo-indolyl aryl sulfones achieve tight binding to drug-resistant mutants by targeting the enzyme-substrate complex." (Insieme di parole chiave)
- Parole chiave di "Indolyl aryl sulphones as HIV-1 non-nucleoside reverse transcriptase inhibitors: synthesis, biological evaluation and binding mode studies of new derivatives at indole-2-carboxamide." (Insieme di parole chiave)
- Parole chiave di "Arylthiopyrrole (AThP) Derivatives as Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors: Synthesis, Structure-Activity Relationships, and Docking Studies (Part 2)." (Insieme di parole chiave)
- Keywords of "The effects of prolonged treatment with zidovudine, lamivudine, and abacavir on a T-lymphoblastoid cell line." (Insieme di parole chiave)
- Keywords of "Towards novel S-DABOC inhibitors: Synthesis, biological investigation, and molecular modeling studies." (Insieme di parole chiave)
- Keywords of "Slow binding-tight binding interaction between benzimidazol-2-one inhibitors and HIV-1 reverse transcriptase containing the lysine 103 to asparagine mutation." (Insieme di parole chiave)
- Keywords of "Prevalence of mutations and determinants of genotypic resistance to etravirine (TMC125) in a large Italian resistance database (ARCA)" (Insieme di parole chiave)
- Parole chiave di "Design, synthesis, biological evaluation, and molecular modeling studies of TIBO-like cyclic sulfones as non-nucleoside HIV-1 reverse transcriptase inhibitors." (Insieme di parole chiave)
- Parole chiave di "Drug treatment of cancer cell lines: a way to select for cancer stem cells?" (Insieme di parole chiave)
- Keywords of "Selective targeting of the HIV-1 reverse transcriptase catalytic complex through interaction with the" (Insieme di parole chiave)
- Parole chiave di "A multidisciplinary approach for the identification of novel HIV-1 non-nucleoside reverse transcriptase inhibitors: S-DABOCs and DAVPs." (Insieme di parole chiave)
- Parole chiave di "Resistance of Schistosoma mansoni to praziquantel: is there a problem?" (Insieme di parole chiave)
- Keywords of "The cyclin-dependent kinase inhibitor roscovitine and the nucleoside analog sangivamycin induce apoptosis in caspase-3 deficient breast cancer cells independent of caspase mediated P-glycoprotein cleavage: implications for therapy of drug resistant breast" (Insieme di parole chiave)
- Keywords of "Nucleoside reverse transcriptase inhibitor resistance mutations associated with first-line stavudine-containing antiretroviral therapy: Programmatic implications for countries phasing out stavudine" (Insieme di parole chiave)
- Keywords of "Model for the Chemotherapy of HIV with Antigenic Variation" (Insieme di parole chiave)
- Parole chiave di "Substrate-Induced Stable Enzyme-Inhibitor Complex Formation Allows Tight Binding of Novel 2-Aminopyrimidin-4(3H)-ones to Drug-Resistant HIV-1 Reverse Transcriptase Mutants." (Insieme di parole chiave)
- Keywords of "Efficacy of ST1968 (namitecan) on a topotecan-resistant squamous cell carcinoma." (Insieme di parole chiave)
- Keywords of "5-Alkyl-6-benzyl-2-(2-oxo-2-phenylethylsulfanyl)pyrimidin-4(3H)-ones, a series of anti-HIV-1 agents of the dihydro-alkoxy-benzyl-oxopyrimidine family with peculiar structure-activity relationship profile." (Insieme di parole chiave)
- Parole chiave di "Novel N1-substituted 1,3-dihydro-2H-benzimidazol-2-ones as potent non-nucleoside reverse transcriptase inhibitors." (Insieme di parole chiave)
- Parole chiave di "Dominant roles of the Raf/MEK/ERK pathway in cell cycle progression, prevention of apoptosis and sensitivity to chemotherapeutic drugs." (Insieme di parole chiave)
- Parole chiave di "Specific targeting highly conserved residues in the HIV-1 reverse transcriptase primer grip region. Design, synthesis, and biological evaluation of novel, potent, and broad spectrum NNRTIs with antiviral activity." (Insieme di parole chiave)
- Parole chiave di "Enhancing therapeutic efficacy by targeting non-oncogene addicted cells with combinations of signal transduction inhibitors and chemotherapy." (Insieme di parole chiave)
- Parole chiave di "Arylthiopyrrole (ATP) Derivatives as Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors." (Insieme di parole chiave)
- Keywords of "Parallel solution-phase and microwave-assisted synthesis of new S-DABO derivatives endowed with subnanomolar anti-HIV-1 activity." (Insieme di parole chiave)
- Parole chiave di "The Raf/MEK/ERK pathway can govern drug resistance, apoptosis and sensitivity to targeted therapy." (Insieme di parole chiave)
- Parole chiave di "High potency of indolyl aryl sulfone nonnucleoside inhibitors towards drug-resistant human immunodeficiency virus type 1 reverse transcriptase mutants is due to selective targeting of different mechanistic forms of the enzyme." (Insieme di parole chiave)
- Parole chiave di "Induction of nuclear receptors and drug resistance in the brain microvascular endothelial cells treated with antiepileptic drugs." (Insieme di parole chiave)
