AIDS

Label

• AIDS (literal)

Membro di

• Keywords of "Diminished RNA-Primer Usage Associated with the L74V and M184V Mutations in Reverse Transcriptase of Human Immunodeficiency Virus Type 1 Provides a Possible Mechanism for Diminished Viral replication Capacity" (Insieme di parole chiave)
• Keywords of "The European Virtual Human Immune System Project" (Insieme di parole chiave)
• Parole chiave di "Mitochondria as agents of disease and as drug targets" (Insieme di parole chiave)
• Parole chiave di "AKAP149 binds to HIV-1 reverse transcriptase and is involved in the reverse transcription." (Insieme di parole chiave)
• Parole chiave di "Discovery of Non-Nucleoside Inhibitors of HIV-1 Reverse Transcriptase Competing with the Nucleotide Substrate." (Insieme di parole chiave)
• Keywords of "AIDS: la verità negata" (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 "Novel N1-substituted 1,3-dihydro-2H-benzimidazol-2-ones as potent non-nucleoside reverse transcriptase inhibitors." (Insieme di parole chiave)
• Keywords of "NNRTI-selected mutations at codon 190 of human immunodeficiency virus type 1 reverse transcriptase decrease susceptibility to stavudine and zidovudine." (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 "Nevirapine resistance mutation at codon 181 of the HIV-1 reverse transcriptase confers stavudine resistance by increasing nucleotide substrate discrimination and phosphorolytic activity" (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 "Characterization of novel N,N-DABOs as effective tight binding non-nucleoside inhibitors of HIV-1 RT." (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)
• Keywords of "Slow-, Tight-Binding HIV-1 Reverse Transcriptase Non-Nucleoside Inhibitors Highly Active against Drug-Resistant Mutants." (Insieme di parole chiave)
• Parole chiave di "Mutation, fitness, viral diversity and predictive markers of disease progression in a computational model of HIV-1 infection" (Insieme di parole chiave)
• Keywords of "Transgenic expression of the deoxynucleotide carrier causes mitochondrial damage that is enhanced by NRTIs for AIDS" (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 "Indolyl aryl sulfones as HIV-1 non-nucleoside reverse transcriptase inhibitors: role of two halogen atoms at the indole ring in developing new analogues with improved antiviral activity." (Insieme di parole chiave)
• Keywords of "N2-Benzyloxycarbonylguan-9-yl Acetic Acid Derivatives as HIV-1 Reverse Transcriptase Non-Nucleoside Inhibitors with Decreased Loss of Potency Against Common Drug-Resistance Mutations." (Insieme di parole chiave)
• Keywords of "?Inibitori non nucleosidici della trascrittasi inversa come induttori del differenziamento cellulare?" (Insieme di parole chiave)
• Parole chiave di "Structure-based pharmacophore identification of new chemical scaffolds as non-nucleoside reverse transcriptase inhibitors." (Insieme di parole chiave)
• Parole chiave di "Synthesis and Biological Properties of Novel 2-Aminopyrimidin-4(3H)-ones Highly Potent against HIV-1 Mutant Strains." (Insieme di parole chiave)
• Parole chiave di "Second generation PBOs show enantioselective binding to the catalytic complex of HIV-1 RT wt and drug resistant mutants." (Insieme di parole chiave)
• Parole chiave di "Pharmacophore modeling and molecular docking led to the discovery of inhibitors of human immunodeficiency virus-1 replication targeting the human cellular aspartic acid-glutamic acid-alanine-aspartic acid box polypeptide 3." (Insieme di parole chiave)
• Keywords of "Natural resistance to HIV infection: role of APOBEC." (Insieme di parole chiave)
• Parole chiave di "Discovery of novel benzimidazolones as potent non-nucleoside reverse transcriptase inhibitors active against wild-type and mutant HIV-1 strains." (Insieme di parole chiave)
• Parole chiave di "New indolylarylsulfones as highly potent and broad spectrum HIV-1 non-nucleoside reverse transcriptase inhibitors" (Insieme di parole chiave)
• Parole chiave di "The balance between the rates of incorporation and pyrophosphorolytic removal influences the HIV-1 reverse transcriptase bypass of an abasic site with deoxy-, dideoxy-, and ribonucleotides." (Insieme di parole chiave)
• Keywords of "6-Vinyl pyrimidine and pyrimidinone derivatives and the use thereof." (Insieme di parole chiave)
• Parole chiave di "Novel HIV-1 NNRTIs with reduced loss of potency against common drug-resistant mutations." (Insieme di parole chiave)
• Parole chiave di "Novel NNRTIs" (Insieme di parole chiave)

Value

• AIDS (literal)

Incoming links:

Ha membro

• Parole chiave di "The balance between the rates of incorporation and pyrophosphorolytic removal influences the HIV-1 reverse transcriptase bypass of an abasic site with deoxy-, dideoxy-, and ribonucleotides." (Insieme di parole chiave)
• Parole chiave di "Pharmacophore modeling and molecular docking led to the discovery of inhibitors of human immunodeficiency virus-1 replication targeting the human cellular aspartic acid-glutamic acid-alanine-aspartic acid box polypeptide 3." (Insieme di parole chiave)
• Parole chiave di "AKAP149 binds to HIV-1 reverse transcriptase and is involved in the reverse transcription." (Insieme di parole chiave)
• Parole chiave di "Mitochondria as agents of disease and as drug targets" (Insieme di parole chiave)
• Parole chiave di "Mutation, fitness, viral diversity and predictive markers of disease progression in a computational model of HIV-1 infection" (Insieme di parole chiave)
• Keywords of "AIDS: la verità negata" (Insieme di parole chiave)
• Keywords of "N2-Benzyloxycarbonylguan-9-yl Acetic Acid Derivatives as HIV-1 Reverse Transcriptase Non-Nucleoside Inhibitors with Decreased Loss of Potency Against Common Drug-Resistance Mutations." (Insieme di parole chiave)
• Keywords of "6-Vinyl pyrimidine and pyrimidinone derivatives and the use thereof." (Insieme di parole chiave)
• Keywords of "Slow-, Tight-Binding HIV-1 Reverse Transcriptase Non-Nucleoside Inhibitors Highly Active against Drug-Resistant Mutants." (Insieme di parole chiave)
• Parole chiave di "Structure-based pharmacophore identification of new chemical scaffolds as non-nucleoside reverse transcriptase inhibitors." (Insieme di parole chiave)
• Keywords of "?Inibitori non nucleosidici della trascrittasi inversa come induttori del differenziamento cellulare?" (Insieme di parole chiave)
• Keywords of "Transgenic expression of the deoxynucleotide carrier causes mitochondrial damage that is enhanced by NRTIs for AIDS" (Insieme di parole chiave)
• Parole chiave di "New indolylarylsulfones as highly potent and broad spectrum HIV-1 non-nucleoside reverse transcriptase inhibitors" (Insieme di parole chiave)
• Keywords of "NNRTI-selected mutations at codon 190 of human immunodeficiency virus type 1 reverse transcriptase decrease susceptibility to stavudine and zidovudine." (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 "Synthesis and Biological Properties of Novel 2-Aminopyrimidin-4(3H)-ones Highly Potent against HIV-1 Mutant Strains." (Insieme di parole chiave)
• Keywords of "Indolyl aryl sulfones as HIV-1 non-nucleoside reverse transcriptase inhibitors: role of two halogen atoms at the indole ring in developing new analogues with improved antiviral activity." (Insieme di parole chiave)
• Keywords of "The European Virtual Human Immune System Project" (Insieme di parole chiave)
• Parole chiave di "Discovery of novel benzimidazolones as potent non-nucleoside reverse transcriptase inhibitors active against wild-type and mutant HIV-1 strains." (Insieme di parole chiave)
• Parole chiave di "Discovery of Non-Nucleoside Inhibitors of HIV-1 Reverse Transcriptase Competing with the Nucleotide Substrate." (Insieme di parole chiave)
• Parole chiave di "Nevirapine resistance mutation at codon 181 of the HIV-1 reverse transcriptase confers stavudine resistance by increasing nucleotide substrate discrimination and phosphorolytic 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)
• 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 "Novel NNRTIs" (Insieme di parole chiave)
• Parole chiave di "Second generation PBOs show enantioselective binding to the catalytic complex of HIV-1 RT wt and drug resistant mutants." (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 "Characterization of novel N,N-DABOs as effective tight binding non-nucleoside inhibitors of HIV-1 RT." (Insieme di parole chiave)
• Parole chiave di "Novel HIV-1 NNRTIs with reduced loss of potency against common drug-resistant mutations." (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)
• Keywords of "Natural resistance to HIV infection: role of APOBEC." (Insieme di parole chiave)
• Keywords of "Diminished RNA-Primer Usage Associated with the L74V and M184V Mutations in Reverse Transcriptase of Human Immunodeficiency Virus Type 1 Provides a Possible Mechanism for Diminished Viral replication Capacity" (Insieme di parole chiave)